Search tips
Search criteria 


Logo of cmrPermissionsJournals.ASM.orgJournalCMR ArticleJournal InfoAuthorsReviewers
Clin Microbiol Rev. 2012 January; 25(1): 106–141.
PMCID: PMC3255962

The Malassezia Genus in Skin and Systemic Diseases


Summary: In the last 15 years, the genus Malassezia has been a topic of intense basic research on taxonomy, physiology, biochemistry, ecology, immunology, and metabolomics. Currently, the genus encompasses 14 species. The 1996 revision of the genus resulted in seven accepted taxa: M. furfur, M. pachydermatis, M. sympodialis, M. globosa, M. obtusa, M. restricta, and M. slooffiae. In the last decade, seven new taxa isolated from healthy and lesional human and animal skin have been accepted: M. dermatis, M. japonica, M. yamatoensis, M. nana, M. caprae, M. equina, and M. cuniculi. However, forthcoming multidisciplinary research is expected to show the etiopathological relationships between these new species and skin diseases. Hitherto, basic and clinical research has established etiological links between Malassezia yeasts, pityriasis versicolor, and sepsis of neonates and immunocompromised individuals. Their role in aggravating seborrheic dermatitis, dandruff, folliculitis, and onychomycosis, though often supported by histopathological evidence and favorable antifungal therapeutic outcomes, remains under investigation. A close association between skin and Malassezia IgE binding allergens in atopic eczema has been shown, while laboratory data support a role in psoriasis exacerbations. Finally, metabolomic research resulted in the proposal of a hypothesis on the contribution of Malassezia-synthesized aryl hydrocarbon receptor (AhR) ligands to basal cell carcinoma through UV radiation-induced carcinogenesis.


Malassezia yeasts are unique under the view that they comprise almost exclusively the single eukaryotic member of the microbial flora of the skin. However, the complexity of the interaction of a unicellular eukaryotic organism (Malassezia) with a tissue of a multicellular organism (skin) makes understanding the interactions and development of disease a complex process. This is easily understood by the fact that once a revision of the genus Malassezia was described in a seminal publication by Guého et al. in 1996 (129), in addition to studying the epidemiology of this yeast in healthy and diseased skin, the need to repeat the already inconclusive experiments in relation to Malassezia immunology surfaced (14). Furthermore, the expansion of our knowledge on the complex homeostatic mechanisms of the skin increases the candidate targets of interactions between this yeast and skin cells.

In this article, in addition to reviewing the taxonomy and identification methods for the currently accepted Malassezia species, an effort is also made to critically assess the available data on Malassezia epidemiology and nosology in humans and the existence of pathogenic subtypes within Malassezia species, their biological characteristics, and their relevance to skin disease. Therapeutic approaches for the treatment of pityriasis versicolor, the prototypical Malassezia-associated skin disease, will be briefly discussed. Furthermore, data on Malassezia systemic infections are reviewed, and provisional diagnostic criteria are proposed.


An overview of the historical events underlying Malassezia taxonomy may be considered prima facie avoidable in the era of metagenomics. To reduce biased interpretations of taxonomic issues, it was deemed essential to refer to the succession of scientific inquiries that in the last 20 years brought about scrupulous research on diverse domains covering Malassezia biology. In many respects, the series of events preceding the current taxonomic status account for the numerous, independently derived theories regarding the role of Malassezia as a skin commensal and pathogen.

Current taxonomy places Malassezia (Baillon) yeasts (19) in the Phylum Basidiomycota, subphylum Ustilaginomycotina, class Exobasidiomycetes, order Malasseziales, and family Malasseziaceae. Today, the genus Malassezia includes 14 lipophilic species that have been isolated from healthy and diseased human and animal skin. However, Malassezia yeasts have been recognized for more than 150 years (91) as members of the human cutaneous flora and etiologic agents of certain skin diseases. As early as the early 1800s, it was noted that yeast cells and filaments were present in the skin scales of patients with pityriasis versicolor (267), whereas yeast cells, but no filaments, were observed in scales from healthy scalp, seborrheic dermatitis scalp, and dandruff. The absence of filaments in seborrheic dermatitis and dandruff lesional scales for many years led to uncertainty regarding the placement of yeast isolates from pityriasis versicolor and those from seborrheic dermatitis and dandruff into the same genus (32, 208, 274). Eventually, Sabouraud (274) placed them into separate genera and named the yeasts forming filaments in pityriasis versicolor skin scales Malassezia furfur and those which did not form filaments in dandruff and seborrheic dermatitis skin scales Pityrosporum malassezii. Almost a decade later, Pityrosporum malassezii was allotted the binomial nomenclature Pityrosporum ovale by Castellani and Chalmers (50) Subsequently, the lipid dependence of the growth of these yeasts was established (127), and it was confirmed that Pityrosporum orbiculare and P. ovale are variants of the same species (97).

From a historical standpoint, it is interesting that isolates from exfoliative dermatitis of a rhinoceros described by Weidman in 1925 (332) and from otitis externa of dogs described by Gustafsson in 1955 (139), although given the names Pityrosporum pachydermatis and Pityrosporum canis, respectively, were in due course found to have similar morphologies. As both isolates did not require lipid supplements for growth in culture, P. canis was accepted as a synonym for P. pachydermatis. Therefore, since 1970, and for approximately 14 years, it was acknowledged that the genus Pityrosporum included three species: P. ovale, P. orbiculare, and P. pachydermatis (292). During that time, the morphological similarities between Pityrosporum and Malassezia, as described by Eichstedt (91) and by Panja (240), were assessed. Hence, in the early 1980s, a reevaluation of those previous studies instigated among taxonomists an unequivocal acceptance of the genus name Malassezia over that of the genus name Pityrosporum. This was based on the morphology, ultrastructure (25, 246), and immunological properties (293, 310) of Malassezia yeasts. In addition, (i) microscopic observations of hyphae in skin scales from pityriasis versicolor lesions and (ii) confirmation of hyphal production by P. orbiculare clinical isolates in culture (87, 233) confirmed its placement in the genus Malassezia. Hence, within the genus Malassezia, the species M. furfur integrated both lipid-dependent yeasts, formerly referred to as P. orbiculare and P. ovale (342). However, toward the end of the 1980s, further studies demonstrated the existence of several M. furfur serovars (69, 221), providing evidence of diversity within the genus, which was observed in vivo as well as in vitro. Following pioneering work based on studies of nuclear DNA G+C content and a DNA-DNA hybridization technique, a new species, Malassezia sympodialis, was defined (290). Eventually, the genus Malassezia was revised and enlarged in 1996 to include 7 species (129). In a description of the new species by Guého et al. (129), conventional and modern spectrum techniques were employed, encompassing morphology, ultrastructure, physiology, and molecular biology. As a result, the genus included seven species, the three former taxa M. furfur, M. pachydermatis, and M. sympodialis and four new taxa, M. globosa, M. obtusa, M. restricta, and M. slooffiae. Lipid dependence for growth remained a common feature among all species, with the exception of M. pachydermatis, and molecular data were in accordance with phenotypic properties, which differed among species. These properties included differential per-species abilities to utilize lipid supplements, catalase and beta-glucosidase reactions, and temperature tolerance at 32°C, 37°C, and 40°C, thus providing a phenotypic identification algorithm for the routine identification of Malassezia isolates to the species level (Table 1). Despite the undisputable value of phenotypic identification, ambiguous results have been reported (132). For example, an accurate differentiation among M. furfur, M. sympodialis, and M. slooffiae isolates is often hindered because results from physiological tests on the basis of Tween compound utilization are very similar (Table 1).

Table 1
Routine phenotypic characterization of 14 Malassezia species based on their identifiable physiological and biochemical propertiesa

Undoubtedly, since the mid-1990s, molecular techniques, and in particular rRNA sequencing analysis (131), advanced Malassezia systematics, linked molecular systematics to the circumscription of new species, and warranted nonculture detection and identification of Malassezia species in patient skin scales from a variety of Malassezia-associated or -exacerbated diseases (114, 119, 295). This also accelerated developments in PCR-based identification methods (Table 2), promoted investigation into Malassezia epidemiology (64, 112) and pathobiology (108), and encouraged research on the association of certain Malassezia species with specific geographical locations (136).

Table 2
Identification of Malassezia species from pure culture by sequencing and/or PCR-based methodsa

In addition, molecular systematics had an impact on the recognition of new Malassezia species associated with human and animal disease. By 2004, three more new species were described: Malassezia dermatis and M. japonica, isolated from Japanese atopic dermatitis (synonym, atopic eczema) patients (299, 300), followed by M. yamatoensis, isolated from healthy human skin and from a patient with seborrheic dermatitis (297). New lipid-dependent species, such as M. nana (150), M. caprae, M. equina (39), and, recently, M. cuniculi (40), from animal skin were also described, raising the number of currently recognized Malassezia species to 14.


Culture-Based Epidemiology

More than 20 studies (Tables 3 to to6)6) have been carried out worldwide on the epidemiology of Malassezia species in cases of pityriasis versicolor, seborrheic dermatitis, atopic eczema, and psoriasis and on healthy control skin of the same individuals or skin from healthy volunteers (53, 63, 89, 112, 122, 146, 171, 173, 180, 185, 228, 237, 255, 259, 275, 286, 344, 353). Results are not directly comparable between studies, as different methodologies, isolation media, and identification procedures have been employed. However, these results can be used for the extraction of interesting conclusions on the epidemiology and pathobiology of Malassezia species. Furthermore, it should be noted that in all those studies, the surface of the skin was sampled and not the hair infundibulum, which is the niche of Malassezia yeasts. From the available data (Tables 3 to to6),6), we can conclude that the 7 Malassezia species described in 1996 (68) are the most common ones, while geographical variations in species distribution are apparent. M. dermatis has been isolated in East Asia (Japan and South Korea), while M. obtusa has been isolated mostly in Sweden, Canada, Bosnia, and Herzegovina but has also been reported in Iran and Indonesia. Identification and typing of the latter isolates with molecular techniques might reveal the existence of atypical M. obtusa-M. furfur subtypes, as these two species are phylogenetically close, and M. furfur shows considerable diversity (106, 315).

Table 3
Results from culture-based epidemiological studies of healthy skin
Table 6
Results from culture-based epidemiological studies of atopic eczema and psoriasis
Table 4
Results from culture-based epidemiological studies of pityriasis versicolor lesions
Table 5
Results from culture-based epidemiological studies of seborrheic dermatitis

Non-Culture-Based Epidemiology

Interesting results have been obtained from studies of Malassezia population dynamics in healthy or diseased human skin employing techniques that directly identify and quantify Malassezia DNA from skin specimens (Table 7). No substantial difference was found in the distributions of Malassezia species subtypes identified in the left and right halves of the body skin of healthy volunteers and psoriasis patients (243, 244). Also, there was no significant difference in the ribosomal DNA (rDNA) sequences of the strains colonizing healthy and psoriasis skin (243, 244). The predominant species in non-culture-based epidemiological studies are M. globosa and M. restricta, which are found on the skin of practically all humans. However, this introduces ambiguity regarding their pathogenic potential, as they are found on healthy and diseased skin equally, thus not fulfilling Koch's postulates. For this reason, the use of robust typing methods, such as multilocus sequencing typing, for the screening of pathogenic versus nonpathogenic Malassezia strains would highlight the pathobiology of Malassezia yeasts.

Table 7
Epidemiological data for non-culture-based methods

Molecular typing of Malassezia yeasts.

Current data (Table 8) point toward the existence of pathogenic subtypes of M. furfur (113, 170, 350), M. globosa (112, 307), and M. restricta (296, 307). The Malassezia microbiota was suggested to be host specific (243). Moreover, for M. furfur, phylogeographic associations have also been found in Greek, Swedish, and Bulgarian strains (106) as well as in the Han and Tibetan ethnic groups in China (350). M. sympodialis seems to represent a homogenous species, with no pathogenic subtypes detected by current molecular methods. However, our current molecular typing approaches are limited, as they provide only indirect evidence on virulence. In that respect, neither the observed sequence variation within the rDNA complex nor the polymorphism determined by PCR-based methods (Table 8) accounts for actual virulence. Essentially, these methods depict disease-associated subtypes that could represent pathogenic lineages whose survival is favored on diseased skin under conditions which are presently inadequately understood.

Table 8
Malassezia species subtypes associated with skin diseasesa


In the ongoing debate on the usefulness of conventional epidemiological studies on the distribution of Malassezia species, it should be noted that more accurate epidemiological data on species distribution can be acquired by non-culture-based molecular techniques. However, conventional culture and identification methods offer the advantage of further evaluating the isolates for possible virulence factors, such as the production of phospholipase (44, 170) and indole (108, 184, 336) and melanin synthesis (107). Furthermore, this was highlighted in a study by Akaza et al. (6), in which the seasonal rates of isolation of Malassezia species from healthy skin determined by quantitative PCR (qPCR) were compared with those determined by use of Leeming-Notman agar (197). Increased Malassezia colonization of the skin in summer was determined by culture but not by PCR. This finding can be attributed to the ability of culture to select viable cells, while PCR also quantifies DNA from nonviable or not metabolically active cells. Furthermore, the initial optimism on the pathogenic potential of M. globosa and its characterization as the causative agent of pityriasis versicolor (63) was subsequently weakened by findings supporting the widespread distribution of this species on healthy skin as well as in seborrheic dermatitis, atopic eczema, and psoriasis skin lesions (Tables 3 to to6).6). The matter is further complicated by the lower rate of recovery of Malassezia yeasts from lesional skin in the latter three skin diseases than from healthy skin, which points toward the existence of metagenomic alterations in the pathogenic strains of Malassezia species in order to survive in the altered environment of diseased skin.


Gradually, experimental data on the multiple facets of the interaction of Malassezia yeasts with different cell types are being collected. Although safe conclusions cannot be drawn, this area of research remains a promising field.

Experimental Data

Malassezia yeasts demonstrate a species-specific ability to interact with cells that are constitutive members of the skin and its adnexal structures, such as various keratinocyte subpopulations, or cell lineages that are involved in immune functions, including antigen-presenting dendritic cells, macrophages, eosinophils, and neutrophils (Table 9). The exposure of the above-mentioned cells to Malassezia yeasts or their products has been shown to induce the production of a variety of cytokines; however, the results are not directly comparable, as different cell lines and protocols have been employed (Table 9). The effect of Malassezia yeasts on cytokine production from keratinocytes in vitro depends on the culture phase of the yeast (stationary versus exponential), on the Malassezia species used, and on the previous manipulations (removal or not) of the yeast cell lipid layer (316). However, this does not universally apply to all the immune response-regulating molecular pathways that operate in epidermal keratinocytes, as it was recently shown that M. globosa and M. restricta could equally efficiently stimulate lysophosphatidic acid receptors in these cells and increase the production of thymic stromal lymphopoietin (160). This property was abrogated when the lipid layer was removed from Malassezia cells. Thymic stromal lymphopoietin may participate in the pathogenesis of atopic eczema, as it can promote a Th2 inflammatory response through corresponding dendritic cell activation. Furthermore, Malassezia yeasts have the ability to bind C-type lectins, which are a diverse group of proteins that have the ability to recognize carbohydrate structures and, upon ligand binding, induce cellular responses with immune and nonimmune functions (128). In mast cells of atopic eczema patients, the expression of dectin-1 and the response to M. sympodialis exposure are modified compared to those of mast cells from healthy individuals (264), and this finding points toward additional host susceptibility factors that interact with Malassezia cellular components and result in the aggravation of atopic eczema. The activation of the C-type lectin Mincle in murine macrophages, through interactions with Malassezia yeasts, led to increases in the induction of tumor necrosis factor alpha (TNF-α), macrophage inflammatory protein 2 (MIP-2), keratinocyte chemoattractant (KC), and interleukin-10 (IL-10) in a yeast/cell-dependent fashion, which was partly reduced in Mincle-deficient cells (340). Although this was originally observed for a strain of M. pachydermatis, binding to Mincle was further confirmed for the lipophilic species M. dermatis, M. japonica, M. nana, M. slooffiae, M. sympodialis, and M. furfur. Another C-type lectin, langerin, characteristically found in epidermal antigen-presenting Langerhans cells, was shown to bind extracts of M. furfur but not M. pachydermatis (79). However, effective binding to both of the latter species was observed when live cells and different Malassezia strains were used (312). Earlier studies showed that the uptake of M. furfur from human monocytes could be abrogated by coculture with soluble mannan and β-glucan (305), possibly through interactions with those receptors. It is most probable that the induction of cytokines from Malassezia cells is not mediated through a single pathway, as it has been shown that mast cell responses can be modulated by Malassezia through the canonical Toll-like receptor 2 (TLR2)/MyD88 pathway but also through a different, not-yet-determined one (282). Interestingly, the contact of Malassezia cells with serum and subsequent opsonization increased their ability to induce IL-8 expression in a macrophage cell line and a granulocytic cell line (304). The differential stimulation of cytokine, chemokine, and adhesion molecule expression in host effector cells (Table 9) would eventually lead to either up- or downregulation of skin inflammatory processes, probably depending on the modifying interactions of still poorly understood cofactors. The resulting deviations in the tissue milieu may be further reflected by the divergent pathophysiologic manifestations of Malassezia-associated skin conditions that span the whole spectrum between overt inflammatory responses (seborrheic dermatitis and atopic eczema) and a distinct absence of inflammation, as in pityriasis versicolor. It can be further speculated at this point that complex interactions between Malassezia yeasts and their commensal or pathogenic microbial bystanders on the skin surface may not only mutually affect the survival and virulence status of both but also serve as decisive modifying cofactors of the pathogenesis of all Malassezia-related skin diseases.

Table 9
Effects of Malassezia interactions with cellsa


The interaction of Malassezia yeasts with the skin immune system is open to further research, and a prospective line of work would be analogous to that already under way for bacterial skin commensals. Species like Staphylococcus epidermidis have the ability to amplify the innate immune response through an increase in the constitutive expression of antimicrobial peptides, which are, however, active against the pathogenic species Staphylococcus aureus (328). A delineation of comparable interaction mechanisms would contribute to a better understanding of the significance of the reported differential colonization of lesional skin by distinctive, “pathogenic” Malassezia species subtypes compared to “nonvirulent” ones associated with healthy skin. Moreover, properly designed experiments could highlight the sequence of internal and external events in the skin microenvironment that mediates the development of Malassezia-associated diseases.


Pityriasis Versicolor

Pityriasis versicolor is the prototypical skin disease etiologically connected to Malassezia species. It is characterized by hypo- or hyperpigmented plaques that are covered by fine scales (pityron, Greek for scale), preferentially distributed in the so-called seborrheic areas of the skin surface, such as the back, chest, and neck (65) (Fig. 1). Vitiligo, pityriasis alba, and leprosy in corresponding areas of endemicity (211) are the main differential diagnoses of pityriasis versicolor. For the clinical differential diagnosis of this disease, Wood's light examination and the so-called “evoked-scale” sign (141, 284) have proven valuable. The latter sign consists of the provocation of visible scales by the stretching or scraping of a pityriasis versicolor lesion, by which the pathologically increased fragility of the lesional stratum corneum becomes evident. Although the exact structural alterations of the stratum corneum that lead to the increased fragility of the stratum corneum in pityriasis versicolor skin lesions are still unknown, it may be that the same aberrations could account for the partial disruption of epidermal barrier function and the increased transepidermal water loss observed for this disease (193). In the case of Wood lamp fluorescence, UV light is emitted at an approximately 365-nm wavelength, and the lesions of pityriasis versicolor will fluoresce reddish or yellowish green. Pityriasis versicolor does not permanently affect the structure of the lesional skin, although some cases that induced nonreversible skin atrophy have been reported (66, 269, 341). Histopathological examination of lesional skin biopsy specimens reveals a slight to moderate hyperkeratosis and, to a lesser degree, acanthosis. Depending on the extent of clinically manifested inflammation, the dermis contains a mild to almost absent superficial perivascular inflammatory cell infiltrate (Fig. 2) consisting mainly of lymphocytes, histiocytes, and, occasionally, plasma cells. Sometimes, mild melanin incontinence is observed. In the stratum corneum, there are numerous budding yeast cells and short hyphae (Fig. 2 and and3).3). Whether rare cases of pityriasis versicolor with interface dermatitis (Fig. 3) (302) are associated with the subsequent development of atrophying lesions is not known.

Fig 1
Pityriasis versicolor in a 42-year-old female patient. The patient had relapsing disease for the past 6 years.
Fig 2
Histopathology of noninflammatory pityriasis versicolor. Shown is the infiltration of the hyperkeratotic stratum corneum by Malassezia cells and hyphae; there is a distinct absence of an inflammatory cell infiltrate. (A) Hematoxylin-eosin stain; (B) PAS ...
Fig 3
Histopathology of inflammatory pityriasis versicolor. Shown is the infiltration of the hyperkeratotic stratum corneum by Malassezia cells and hyphae; there is a moderately dense perivascular inflammatory cell infiltrate in the upper dermis. (A) Hematoxylin-eosin ...

Pityriasis versicolor has been reported to appear in all age groups, ranging from infants 4 months old (84) to children (314), adults, and elderly individuals (85). However, the prevalence of this common skin disease is greater in the third and fourth decades of life, and its appearance is significantly affected by environmental factors such as temperature and humidity, patient immune status, and genetic predisposition. The annual incidence of pityriasis versicolor has been reported to range from 5.2% to 8.3% (93). Seasonal variations, although not consistent, are observed, with the highest incidence rates in September (314), spring and fall (55), or summer months (144). If not corrected for these variations, records on the prevalence of pityriasis versicolor in a population may be affected, but nevertheless, this disease is significantly more common in tropical and subtropical climates (93). The prevalence of the disease falls drastically in more temperate climates, as it was diagnosed in only 2.1% of young healthy males (mean age, 22 years) in Italy (156), with even lower rates in Sweden (0.5% of males and 0.3% of females) (147). The peak age-specific prevalence of pityriasis versicolor is among young adults 20 to 40 years old (189); however, in tropical/subtropical regions, such as India, the highest disease prevalence has been recorded for somewhat younger individuals, between 10 and 30 years old (89). Pityriasis versicolor is not an infectious disease, and hereditable factors decisively contribute to its appearance. A positive family history of pityriasis versicolor has been found for approximately 20% of patients (140, 144) in relevant studies without conjugal cases reported for married couples (144). Also, a polygenic additive-inheritance model of susceptibility to this disease was observed in one of these studies (144). The reported differences in the male-to-female ratio are suggestive of a sampling or reporting bias, as expected for a fluctuating disease without alerting symptoms. The burden of pityriasis versicolor might not be that evident in light-colored Caucasians but can represent social stigmatization when extensive depigmentation happens in colored skin.

Pityriasis versicolor and Malassezia.

Besides the consistent description of yeasts from pityriasis versicolor lesions, there are two main facts that permit an etiologic association of Malassezia with this disease: (i) it is more likely that a positive culture will be obtained from specimens taken from lesional skin than from macroscopically unaffected skin areas of either the same individual (255) or matched healthy controls (275), and (ii) the hyphal state is connected to pityriasis versicolor lesions, independently of the Malassezia species isolated, and seems to play an important role in the pathogenesis of this disease (127). However, the expansion of hyphae in pityriasis versicolor patients is not confined to lesional skin. This points to a global propensity of the skin of these patients, at least at the time of overt disease, to support the hyphal growth of Malassezia species. Rates of isolation of hyphae from nonlesional trunk skin (42%) and the head (50%) of patients with pityriasis versicolor were lower than those reported for the lesions per se (100%) but were more than those reported for the skin of healthy individuals (6 to 7%) (217). As mentioned above, the Malassezia species initially associated with pityriasis versicolor was M. globosa (63), but current epidemiological data as well as the absence of distinct virulence factors confined to this species (151) do not permit a definite conclusion.

The involvement of Malassezia yeasts in the development of pityriasis versicolor illustrates the excellent adaptive mechanisms which this yeast possesses, with relevance to human skin physiology. In the two most common clinical forms of this disease, the hyperpigmented and hypopigmented forms, there is a significant fungal load on the skin but without any inflammatory alterations being observed. This has been partly attributed to the production of an array of indolic compounds produced by Malassezia species, in particular M. furfur (213), that have the ability to downregulate aspects of the inflammatory cascade (see below). Thus, indoles like pityriarubins impede the respiratory burst of human neutrophils (183), while indirubin and indolo[3,2-b]carbazole inhibit the phenotypic maturation of human dendritic cells (324). Additionally, malassezin was proposed to induce apoptosis in human melanocytes, and pityriacitrin was initially shown to have UV radiation-absorbing properties (206, 215). Due to its UV-absorbing capacity, it was proposed that it protects the underlying skin in the hypopigmented plaques of pityriasis versicolor (pityriasis versicolor alba) (190). However, this was not confirmed in subsequent in vivo and in vitro experiments (116), suggesting that additional substances may contribute to the clinically observed UV resistance of lesional skin. For the synthesis of these compounds, tryptophan aminotransferase, which converts l-tryptophan to indolepyruvate, has been inferred to be an important enzymatic step from data acquired from the phylogenetically close phytopathogenic yeast Ustilago maydis (355). The inhibition

of this enzyme by cycloserine led to the clinical reversal of hyperpigmented pityriasis versicolor lesions in vivo (214). The synthesis of these indoles is widely distributed among Malassezia species, and since this trait is also associated with the respective pathogenic potential of M. furfur (108) (P. Magiatis et al., unpublished data), the existence of additional biosynthetic pathways cannot be excluded.

Other metabolites that have been linked to the clinical presentation of pityriasis versicolor include melanin (107), azelaic acid (232), and other products of skin lipid peroxidation (80). The in vitro production of melanin by l-3,4-dihydroxyphenylalanine (l-DOPA) has been documented; however, the observation of melanized Malassezia cells in vivo in hyperpigmented lesions of pityriasis versicolor (107) still remains to be confirmed by relevant clinical studies. Finally, the proposed attribution of lesional skin hypopigmentation to the known competitive inhibition of tyrosinase activity by Malassezia-produced azelaic acid is most probably not relevant to the clinical setting, as this dicarboxylic acid cannot be synthesized in biologically significant quantities on diseased skin (196).


As mentioned above in the introduction, treatment for pityriasis versicolor will be discussed only briefly, and readers are referred to a recent relevant meta-analysis for further details (153). The goal of both topical and systemic treatments of pityriasis versicolor is not to eradicate Malassezia from skin but to restore the yeast's population dynamics to the commensal status.

In general, longer treatment periods (up to 4 weeks) and higher concentrations of topical regimens or doses of systemic agents result in higher cure rates, without, however, avoiding the increased relapse rate (153). In the latter case, prophylactic treatment regimens have been suggested.

Topical treatments are generally well tolerated and highly effective compared to placebo. Among the topical regimens, shampoos containing fungicidal concentrations of antifungal imidazoles, applied once daily for up to 4 weeks, were found to be adequately effective for the treatment of pityriasis versicolor (83). However, older studies also documented that nonimidazole topical agent formulations (zinc pyrithione shampoo, sulfur-salicylic acid shampoo, and selenium sulfide lotion) are sufficiently effective treatment options compared to placebo (21, 104, 276). More recently, pathophysiologically designed topical therapeutic approaches that target certain aspects of pityriasis versicolor pathogenesis are under clinical evaluation. Among them, quite promising approaches seem to be a 10-day application of a nitric oxide-liberating cream (168); the application twice daily of a 0.2 mol liter−1 aqueous cycloserine solution for 5 days, which resulted in the complete healing of hyperpigmented pityriasis versicolor with a rapid correction of the pigment deviation (214); and 5-aminolevulinic acid photodynamic therapy for regionally confined lesions (179).

Extensive pityriasis versicolor can be treated successfully and safely with different oral antifungals (ketoconazole, itraconazole, and fluconazole) applied at a rather wide range of doses (range of up to 4×) and for treatment periods of 7 to 28 days (153). This is also the case with the use of newer imidazoles, like pramiconazole (100). Currently, the efficacy of single-dose regimens with different oral imidazoles to improve compliance is under clinical evaluation (78, 326).

Pityriasis versicolor prophylaxis approaches are not well documented. Two older trials reported that itraconazole at 200 mg twice daily, once per month, sufficiently reduced the rate of disease relapses compared to placebo (see reference 153). Optimal preventive regimens employing other oral antifungals or topical formulations have not been adequately evaluated to date.


The relationship between pityriasis versicolor and Malassezia still remains an obscure one despite the frequency of this skin disease and the confirmed association with Malassezia. However, dissecting the mechanisms that trigger this skin disease would expand our knowledge on Malassezia and skin adaptive homeostatic mechanisms.

Seborrheic Dermatitis

Seborrheic dermatitis (synonym, seborrheic eczema) is a relapsing skin disease that shows a predilection for the so-called seborrheic areas of the skin, such as the scalp, eyebrows, paranasal folds (Fig. 4), chest, back, axillae, and genitals, and is characterized by recurrent erythema and scaling. However, it should also be stressed that despite its designation, seborrhea is not present in seborrheic dermatitis (37). No widely accepted criteria regarding the diagnosis and grading of seborrheic dermatitis exist, and identification can constitute a clinical problem for psoriasis patients with facial involvement, a condition termed sebopsoriasis. Seborrheic dermatitis was initially described by Unna (318), and the association with Malassezia yeasts was accepted up to the middle of the 20th century, when the observed increased epidermal cell turnover gradually prompted researchers to characterize this condition as being intrinsic to the skin, analogous to psoriasis. The recognition of the role of Malassezia yeasts in seborrheic dermatitis pathogenesis was reappraised in the 1980s, when it was shown that the common denominator of the multiple treatment regimens used for seborrheic dermatitis was their antifungal activity (288).

Fig 4
Seborrheic dermatitis in the nasolabial folds. The distribution of the lesions is typical; however, the seborrheic dermatitis can be characterized as severe, as the disease is extended into the parietal region and is associated with intense erythema and ...

The prevalence of seborrheic dermatitis is high, reaching 11.6% in a study from the United States, while dermatologists had diagnosed this condition in 2.6% of men and 3.0% of women in a relevant study (229). The disease is more common in certain populations, such as the elderly (181), and can be severe and therapy resistant in neuroleptic-induced Parkinsonism (31) and HIV patients (227). The occasionally observed clinical resistance to azole drugs in some cases of seborrheic dermatitis could be attributed to variable genotypes of the recently described M. globosa azole-metabolizing CYP51 enzyme (177).

The prevalence of seborrheic dermatitis peaks when sebaceous gland activity is high (15), during the first 3 months of life (infantile seborrheic dermatitis) and during puberty, but also when sebum excretion is reduced after the age of 50 years (61). Seborrheic dermatitis flares are also observed in the fall, when the level of sebum production is decreased compared to that in summer (345). The flare of disease could be associated with altered population dynamics, which would be affected not only by variations in sebaceous gland activity but also by modifications in other nutrients supplied by sweat, such as essential amino acids like glycine and tryptophan (148). It has been shown in vitro that glycine stimulates the fast growth of M. furfur, and when this amino acid is exhausted, yeast cells employ tryptophan as a nitrogen source, increasing the production of indolic metabolites (24). Such cycles of population growth, bioactive indole production, and subsequent deprivation of nutrients could result in insufficiently masked antigens and ligands on the surface of the yeast cells, which would result in the activation of the immune system. One study showed that increased numbers of metabolically active cells during summer resulted in higher rates of isolation in culture medium than in fall, although the actual DNA loads were equal in both seasons (6). The difference in the rates of active versus stationary/dead yeasts cells would result in the differential regulation of the skin immune response (316).

Seborrheic dermatitis and Malassezia.

Currently available data are not sufficient to define Malassezia virulence factors that lead to the appearance or exacerbation of seborrheic dermatitis. It should be noted that skin is the niche of Malassezia, and the interplay of the yeast with keratinocytes and immune cells determines the transformation of this commensal to a pathogen.

Environmental factors, such as UV radiation and antagonistic microorganisms, may constitute stress factors similarly for Malassezia yeasts and the skin. Thus, the ability of Malassezia to locally modify the immune response, in addition to host susceptibility and the production of secondary metabolites by the yeast, probably participates in eliciting and maintaining seborrheic dermatitis. Higher production rates of aryl hydrocarbon receptor (AhR) ligands in vitro by M. furfur have been associated with seborrheic dermatitis isolates (108). AhR is found in sebocytes (169), and its function is modified by epidermal growth factor receptor (EGFR) (268, 301). The latter probably has a seborrheic distribution, as antibodies or small molecules that block its function cause a folliculocentric eruption with a seborrheic distribution (36), and the interplay of these two receptors was proposed previously (105). Thus, an initial approach to understanding the participation of aryl hydrocarbon receptor in seborrheic dermatitis would be to study polymorphisms of the implicated downstream proteins (218) in patients and healthy controls and associate them with the indole-producing capacity of Malassezia strains that are isolated from their skin.

Current evidence demonstrates that seborrheic dermatitis results from a nonspecific immune response to Malassezia yeasts. Unfortunately, very few experiments were performed after the identification of new Malassezia species, and this is reflected in the available data (Table 9). Inflammatory markers recorded by immunocytochemistry of skin biopsy specimens from seborrheic dermatitis lesions show an increase in levels of inflammatory mediators (interleukin-1α [IL-1α], IL-1β, IL-2, IL-4, IL-6, IL-10, IL-12, gamma interferon [IFN-γ], and tumor necrosis factor alpha [TNF-α]) in the epidermis and around the follicles of diseased skin (98). These inflammatory markers are equivalent to those produced by Malassezia yeasts in experimental models (Table 9). However, this increase did not differ statistically from levels in adjacent, healthy-looking skin and varied only from levels on the skin of healthy volunteers (98), suggesting an individual susceptibility to the development of seborrheic dermatitis. Furthermore, Malassezia yeasts demonstrated an ability to induce immune reactions, depending on the species, the culture growth phase, yeast cell viability, and the integrity of Malassezia cells (316) (Table 9). The 2 species that are commonly isolated from human skin (M. globosa and M. restricta) demonstrate distinct profiles of proinflammatory cytokine production from epidermal cells, with M. globosa stimulating the production of significantly more cytokines than M. restricta. However, the net effect of this cytokine synthesis, i.e., immune stimulation or tolerance, cannot be extracted from published data, as experimental conditions are not comparable (Table 9). For example, even the use of different culture media could result in different compositions of the lipid layer that covers the cell wall of Malassezia, resulting in a variable modulation of the immune system (316). In a recent study, the levels of binding and activation of the C-type lectin Mincle caused by Malassezia yeasts were higher than those of other fungi (340). However, the growth of Malassezia yeasts in a medium with only olive oil as a lipid source would have resulted in an insufficient masking of mannose residues that could subsequently be recognized by Mincle (340).

Another virulence factor intrinsic to Malassezia yeasts that has been discussed in association with the pathogenesis of seborrheic dermatitis is the production of phospholipases and the response to β-endorphin. The increased level of production of phospholipase after β-endorphin stimulation has been shown only for pathogenic M. pachydermatis strains; however, there is evidence that this also applies to lipophilic Malassezia species, although to date, this has been reproducible in vitro only for M. furfur (323). However, sebum production is increased by β-endorphin (354), and the demonstration of a functional μ-opioid receptor in pathogenic and nonpathogenic M. pachydermatis strains (41, 42, 44) has been shown. This points toward the existence of an equivalent sensory pathway in the lipophilic Malassezia species that could assist in the preparation of the yeast for a better utilization of sebaceous lipids. The aberrant production of Malassezia phospholipases on the skin could result in the removal of epidermal lipids, disruption of the epidermal barrier function, and the development of seborrheic dermatitis when sebum production is constitutionally decreased. Phospholipase production is a well-established virulence factor in Candida albicans (187), and the existence of environmental sensory G-protein-coupled receptors in fungi has been shown (339). Mining of the sequenced genome of M. globosa would lead to the recognition and detection of relevant genes in Malassezia and their association with the pathogenetic potential of the respective strains.

Malassezia, seborrheic dermatitis, and HIV/AIDS.

Seborrheic dermatitis in HIV/AIDS patients is more severe and more recalcitrant to treatment and advances with the stage of the disease (227). HIV/AIDS is associated with the development of multiple skin diseases; however, seborrheic dermatitis is the most common, with its reported prevalence ranging between 20 and 40% in HIV-1-seropositive patients and between 40 and 80% in those with AIDS (317). The keratinocyte response to stress signals (258) as well as the cross talk of Langerhans cells with CD-4 memory lymphocytes are modified in HIV/AIDS patients, and the skin immune system is disorganized by the destruction of both subsets of immune cells (249). Data from Malassezia population studies of HIV/AIDS-associated seborrheic dermatitis are inconclusive, as increased numbers of Malassezia yeasts have been found on the skin of HIV/AIDS-positive volunteers without seborrheic dermatitis (245) and on the healthy skin of HIV-positive seborrheic dermatitis patients (245) compared to controls. However, decreased Malassezia numbers in HIV patients with seborrheic dermatitis (227, 335) have also been reported, calling into question the implication of Malassezia yeasts (335). It is conceivable that as HIV/AIDS advances, the skin immune system disintegrates and, therefore, multiple treatment-resistant viral, bacterial, and fungal dermatoses develop (165), challenging the survival of commensal Malassezia yeasts and prompting them to express virulence factors.

Malassezia and infantile seborrheic dermatitis.

Infantile seborrheic dermatitis describes a characteristic, usually nonpruritic, eczematous or psoriasiform eruption that usually appears between the second week and the sixth month of life and can involve the face, scalp, trunk, and sternum area, individually or in any combination (15, 343). The lesions might coalesce, especially on the face and flexures, but when on the trunk, they are more distinct. The microbial flora of the mothers seems to pass to the lactating infant during breastfeeding and readily colonizes the skin within the first 24 h of life (G. Stamatas, unpublished data). During rapid expansion in order to cover the infant skin biocene (i.e., the absence of living microorganisms), the interaction with the still immature neonatal immune system and the epidermis, itself adapting to its new environment, could cause seborrheic dermatitis.

Malassezia and dandruff.

Dandruff is a poorly defined, frequent, pathological skin condition confined to the scalp and is characterized by flaking with minimal to absent inflammation. Dandruff improves after reducing the population of Malassezia yeasts on the scalp with proper treatment (133). However, the experimental application of oleic acid has resulted in the production of dandruff lesions only in dandruff-prone individuals (75). Oleic acid in the scalp is produced from the hydrolysis of triglycerides by Malassezia lipases (74). A variety of lipases has been shown to be encoded by M. furfur (35), M. pachydermatis (285), and M. globosa (76). The expression of M. globosa lipases on the scalp of humans has been shown (76), increasing the significance of this observation and supporting a link between clinical observations (75) and experimental data (35, 76, 285).


Current data highly implicate Malassezia yeasts in the pathogenesis of both seborrheic dermatitis and dandruff. However, despite the global distribution and significant economic burden that these skin conditions inflict, amazingly, limited research has been conducted to date to improve our knowledge concerning the exact role of Malassezia in their pathogenesis. Nevertheless, both seborrheic dermatitis and dandruff represent excellent models for understanding the species- and strain-specific metabolic and immunogenic potential of Malassezia yeasts as well as host susceptibility.

Atopic Eczema

Atopic eczema (166) is a multifactorial skin disease with a diverse genetic background, and it is characterized by a distinct constellation of clinical symptoms and signs. Currently, the interplay between an inherently defective skin barrier (60) and an aberrant skin immune response (77) constitutes the most widely accepted pathophysiological concept for the understanding of the pathogenesis of this skin disease. Malassezia yeasts have species- and strain-specific properties that support a distinctive, probably more than simply modifying, role in the pathogenesis and maintenance of atopic eczema. Despite the fact that there is no definite conclusion regarding the timing of events that result in the development of atopic eczema (a barrier defect predisposes one to immune stimulation, or an immune defect causes barrier damage) (30), resident Malassezia yeasts could actively participate in the deregulation of the skin homeostatic mechanisms.

Malassezia and atopic eczema.

The anatomical substrate of the epidermal barrier function, which is defective in atopic eczema (60), is the stratum corneum of the epidermis, a thin biological membrane that covers the whole body surface. It is made up of the keratinized, terminally differentiated epidermal keratinocytes of the interfollicular epidermis bound together by corneodesmosomes, filled with natural moisturizing factor and embedded in a lipidic matrix that is composed mainly of ceramides, cholesterol, fatty acids, and cholesterol esters (60). The natural moisturizing factor is formed by the degradation of fillagrin, comprising substances such as lactic acid, sodium pyrrolidone, carboxylic acid, urocanic acid, and urea (60). Decisive for the proper function of the stratum corneum is the maintenance of a pH gradient between its acidic outer and basic inner surfaces that motors many vital functions of this life-imperative biological membrane. Constitutional genetic defects in the formation of this barrier can be aggravated by the action of commensal organisms like Malassezia yeasts. The production of proteinase and phospholipase has been shown for the mainly animal M. pachydermatis isolates (62) and has been correlated with disease severity in dogs (205). Furthermore, phospholipase production as a response to β-endorphin stimulation, possibly through the expression of β-opioid-sensing receptors, has also been shown for M. pachydermatis (42) but has not been confirmed for human lipophilic isolates (323). However, the production of multiple secreted lipases by M. globosa, as predicted by recent sequencing results (338), suggests the presence of an enzymatic mechanism that, in addition to utilizing the secreted sebum lipids, could further downgrade (74) the already compromised lipidic constituents of the atopic epidermal barrier.

The damaged epidermal barrier function coupled with the vicious itching-and-scratching cycle in atopic eczema would allow the penetration of whole and fragmented cells that could activate innate immunity and sensitize adaptive immunity in these patients (77, 334). As mentioned above, Malassezia yeasts stimulate keratinocytes to produce a variety of cytokines in a species-dependent manner (Table 9). When healthy-looking atopic skin was patch tested with M. sympodialis ATCC 42132 extract, it demonstrated a gene expression profile similar to that of diseased skin (273). This profile showed increased levels of expression of inflammation- and immune function-associated genes and the downregulation of genes associated with skin lipid production in samples taken from both sites. Overall, these data show that at least M. sympodialis has the ability to induce an atopic eczema profile in vivo in susceptible individuals.

At some point in the evolution of disease in an individual with atopic eczema, sensitization to Malassezia allergens can occur with the production of Malassezia-specific IgE (Table 10). The level of total IgE in the serum of subjects with atopic eczema correlates with disease severity and currently permits the discrimination of 2 clinical types of atopic eczema according to IgE levels, “extrinsic” and “intrinsic” atopic eczema (30), with high and low levels of IgE antibodies, respectively. The progression of the latter form to the former is considered possible during the course of the disease. Notably, sensitization to M. sympodialis may happen in atopic eczema patients with both forms of the disease. Furthermore, sensitization to Malassezia yeasts is specific for the skin manifestations of this disease and does not happen in atopic patients with mostly respiratory symptoms like rhinoconjuctivitis and/or asthma or in patients with other hypersensitivity skin syndromes, like urticaria (48). The extent of this sensitization varies according to the recombinant allergen used for testing and is greater for antigens that could present higher degrees of cross-reactivity with human proteins, such as Mala s 6, which demonstrates structural similarity with cyclophilin (Table 10). It was recently shown that the M. sympodialis allergen Mala s 13 (thioredoxin) can cross-react with human recombinant thioredoxin, stimulating skin and peripheral blood lymphocytes toward a Th1, Th2, and Th17 inflammatory phenotype. In M. sympodialis-sensitized atopic eczema patients (20), these cells not only cross-react with human thioredoxin but also express skin homing markers. Furthermore, when human skin keratinocytes were exposed to a variety of cytokines (gamma interferon, tumor necrosis factor alpha, and interleukin-4), they released significant quantities of thioredoxin into the medium, pointing toward an additional triggering pathway of atopic eczema in this group of patients (20).

Table 10
Malassezia allergens

Malassezia allergens.

IgE binding allergens have been identified in M. sympodialis, M. furfur, and, lately, M. globosa (Table 10). Although M. globosa is the most common species on human skin, and most atopic eczema patients present IgE reactivity to M. globosa antigens (347), only recently has research work focused on the identification and isolation of relevant allergens (159). The identified allergen, provisionally termed MGp42, has a molecular mass of 42 kDa and reacted with the sera of all atopic patients included in that study. This allergen corresponds to heat shock protein 70 (HSP70) of yeast, and interestingly, it demonstrates a higher level of sequence identity to the human (65%) or Penicillium citrinum (75%) protein than to the analogous M. sympodialis Mala s 10 allergen (22% sequence identity). However, despite the significant structural homology, further testing of MGp42 could not demonstrate noteworthy cross-reactivity with human HSP70, which was attributed to alterations in binding epitopes due to steric hindrance (159).

The best-studied Malassezia allergens are those identified for M. sympodialis (Table 10), and two types of these can be distinguished. The first type demonstrates sequence similarity to human proteins (Mala s 5, 6, and 10 to 13 and Mala f 2, 3, and 4) and cross-reactivity with relevant human proteins, and the second type (Mala s 1 and 7 to 9) demonstrates no similarity with any known protein, and thus, their function cannot be determined (110). Among the described M. sympodialis allergens, Mala s 11 possesses a high degree of sequence identity to the human mitochondrial enzyme manganese superoxide dismutase as well as to the homologous Aspergillus fumigatus enzyme (321). The residues that are responsible for IgE binding have been shown to partly correlate with those of the human enzyme (321). The complexity of the genus Malassezia is further highlighted by the structure of the major allergen of M. sympodialis, termed Mala s 1. This allergen has sequences that are found only in this particular species (109) and also demonstrates a crystallized 6-fold-β-propeller structure, a novel fold among allergens (322).


The implication of Malassezia yeasts in atopic eczema is currently under intense investigation, and more studies are needed in order to understand the exact role of these organisms in disease courses and exacerbations. However, the recognition of IgE binding allergens produced by Malassezia yeasts and the observed selectivity of the response of immune cells to Malassezia point toward a close association between the skin and its predominant eukaryotic symbiont.


The association of Malassezia yeasts with psoriasis was first proposed by Rivolta (266), with a description of Cryptococcus psoriasis isolated from the epidermis of psoriasis patients. The yeast was described as double-contoured budding cells, later considered to correspond to Malassezia yeasts. However, the complexity of psoriasis pathogenesis and the ambiguous therapeutic potential of antimycotic drugs support only a secondary role, possibly that of an exacerbating factor, for Malassezia yeasts in psoriasis. Patch testing with sonication-killed M. furfur cells in psoriatic patients and controls succeeded in activating the disease in 10/10 patients, in comparison to 2/10 controls (202). In a psoriatic patient, guttate psoriatic lesions with compatible histology appeared in pityriasis versicolor lesions and subsided after fluconazole treatment (230). In another case report, guttate lesions of psoriasis developed in areas of Malassezia folliculitis (92). Also, the reverse has been observed, with recurrence of pityriasis versicolor after the healing of psoriasis following treatment with etanercept (198). However, the initial encouraging results for the treatment of scalp psoriasis with antifungal drugs (101, 271) have not been established in subsequent studies.

As mentioned above, epidemiological data on the distribution of Malassezia species in psoriasis lesional skin are contradictory (Tables 6 and and7),7), and diminished Malassezia numbers have been reported for healthy-looking and lesional skin of psoriasis patients (243, 244, 353). Also, pathogenic strains, like those established for pityriasis versicolor, atopic eczema, and seborrheic dermatitis, have not been found in cases of psoriasis (244). A possible explanation for this could be the relative scarcity of studies compared to the number of studies on other Malassezia-associated skin diseases. However, the recent pathogenesis model of psoriasis in genetically susceptible individuals includes the triggering of lesions by complexes formed from self-DNA released by stressed keratinocytes and the cathelicidin antimicrobial peptide LL-37, which subsequently stimulates plasmacytoid dendritic cells to secrete IFN-α, thus initiating and sustaining psoriasis lesions (234). A constitutionally excess production of antimicrobial peptides by psoriatic keratinocytes could be responsible for the diminished Malassezia population on psoriatic skin, but on the other hand, their production could also be secondarily exaggerated by Malassezia yeasts invading the skin and stressing predisposed keratinocytes (28). Thus, the resulting increase in the level of production of LL-37 (2) might contribute to the triggering of psoriasis lesions. Furthermore, the activation of TLR2 in keratinocytes seems to participate in the pathogenesis of psoriasis, most probably through the above-mentioned cathelicidin pathway. Malassezia yeasts have been shown to induce the TLR2 pathway (26). However, only to demonstrate the complexity of the participation of Malassezia yeasts in psoriasis pathogenesis, indirubin, a Malassezia-synthesized indole, was successfully employed for the treatment of this disease (200).

In conclusion, the role of Malassezia yeasts in exacerbations of psoriasis, especially on the scalp, will move in parallel with the eventual unraveling of the cause of psoriasis pathogenesis and the virulence characteristics of this yeast.

Malassezia Folliculitis

Malassezia folliculitis appears in the upper trunk, i.e., shoulders, back, and chest, and pruritus is a frequent symptom (Fig. 5). Occlusion is a common predisposing factor (18), especially for susceptible individuals (126), and the condition is also associated with immunosuppression (8, 226, 263); however, in these patients, it may appear with less distinct pruritus (65). Histopathological sections reveal dilated, partly destructed hair follicles, which contain keratinous material, debris, and, sometimes, mucin. Usually, a mild to moderate chronic inflammatory cell infiltrate encapsulates the infundibular portion of the affected follicle (Fig. 6). On periodic acid-Schiff (PAS)-stained sections, the presence of Malassezia yeasts becomes evident in the form of small spherical-to-oval yeast organisms without the regular observation of hyphae (250). There seems to be some predisposition to the development of Malassezia folliculitis along with other Malassezia-associated diseases like pityriasis versicolor and seborrheic dermatitis (99). It is more common in hot and humid environments and has been reported to coexist in 56% of acne patients in the Philippines (163) and to be present in 1 to 1.5% of dermatology outpatients in China (36). Thus, because of clinical similarities, this condition might be underdiagnosed in patients with acne (16). Also, Malassezia folliculitis in the form of an epidemic in an intensive care setting (12) and in heart transplant recipients (263) has been reported. However, it is rather rare in pregnancy (186), despite the corresponding relative immunosuppression.

Fig 5
Malassezia folliculitis in a 34-year-old construction worker. The condition developed after working in a hot, humid environment for a few days. (A) Back of the patient. (B) Close-up view of the lesions.
Fig 6
Histopathology of Malassezia folliculitis. (A) Dilated hair follicle filled with keratinous material and basophilic debris. Shown is a perifollicular inflammatory cell infiltrate with hematoxylin-eosin staining. Original magnification, ×40. (B) ...

The pathogenesis of Malassezia folliculitis is incompletely understood, but recent evidence shows that it is the normal cutaneous flora that infects the hair follicle and leads to the development of folliculitis (5). Thus, the most common species identified are M. restricta, M. globosa, and M. sympodialis, either alone or in association with each other (5). An older report assessing the use of ketoconazole for Malassezia folliculitis attributed the observed therapeutic effectiveness to the reversal of the follicular occlusion from the drug and not to its antifungal effects (149). In the future, studying the population of patients who develop Malassezia folliculitis under modern biologic therapies, pharmaceutical agents that also intervene with complex cellular signals, might prove more effective for the understanding of the pathophysiology of Malassezia folliculitis. Thus, this rash has been observed for patients receiving anti-tumor necrosis factor alpha medication (infliximab) for inflammatory bowel disease (231); erlotinib, an epidermal growth factor receptor tyrosine kinase inhibitor, for renal carcinoma (68); and cetuximab for parotid gland adenocarcinoma (56).


Different reports in the literature have linked Malassezia yeasts with cases of onychomycoses. However, even in the most well-established cases (57), the question remains whether Malassezia has the ability to invade the nail, as no keratinolytic capacity has been demonstrated to date. However, in a case described by Chowdhary et al. (57), the nail invasion of M. furfur was proven by histopathology; the pathogenic strain was isolated more than once and was identified by conventional and molecular (sequencing) techniques. In addition, other comorbidities that could affect the nail plate, like psoriasis, were excluded. However, those authors remained skeptical, suggesting that M. furfur onychomycosis could have resulted from an initial damage of the nail plate by Candida albicans. Reported Malassezia onychomycosis case series include those describing laboratory personnel who handled these yeasts (67) and immunocompromised patients (67). In one study, 370 screened patients had a diagnosis of fungal onychomycosis, and a Malassezia isolate was involved in 14 cases (289), but in 3 cases, it was coisolated with Candida albicans or Trichophyton rubrum, which could have been the primary pathogen. Recent cases involved extended hand nail plate damage in a 26-year-old woman (351) and involvement of all hand nails in a 34-year-old male worker (349) and a liver transplant patient (95). Although the therapeutic criterion was stated in the reported cases, the absence of a possible pathogenetic mechanism as well as the lack of a constant source of lipids under the nail plate do not support a role for Malassezia yeasts, at least as primary pathogens, in onychomycosis.

Malassezia in Systemic Infections

The first report of a systemic infection caused by the alleged “innocent” basidiomycetous yeast Malassezia was described in 1979 (327) and complicated the continuous ambulatory peritoneal dialysis of a patient with chronic renal failure. The increased number of immunosuppressed individuals susceptible to rare fungal pathogens (143) append Malassezia yeasts as candidate pathogens in adult and neonatal intensive care units (ICUs).

As the majority of cases were reported prior to the implementation of the new taxonomy for Malassezia yeasts, the genus name Malassezia sp. will be used in order to address cases of lipophilic yeast systemic isolates characterized as M. furfur (sensu lato) or Pityrosporum ovale, while M. pachydermatis will be used for nonobligatory lipophilic isolates.

The majority of published case reports and miniepidemics have involved infants, children, and adults with profound immunosuppression, serious concurrent health problems, and the infusion of total parenteral nutrition (TPN) with lipid supplementation (LS) through central vascular catheters (CVCs). Apart from systemic infections caused by the nonobligatory lipophilic yeast M. pachydermatis, the infections caused by the lipophilic Malassezia species are divided here into an infant group and into a second group that includes pediatric and adult patients (Table 11).

Table 11
Demographic information, clinical and laboratory findings, therapeutic approaches, and outcomes of Malassezia furfur (sensu lato) systemic infections and miniepidemics in neonates reported in the English-language literature from 1981 to 2011a

M. pachydermatis infections.

The first case of M. pachydermatis infection was described in 1983 in an insulin-dependent diabetic patient on continuous ambulatory peritoneal dialysis who was admitted for weight loss, diarrhea, and cloudy “sterile” peritoneal effluent (103). M. pachydermatis was isolated in culture following repeated positive microscopy results for yeast cells in the effluent. The simple removal of the peritoneal catheter and treatment of renal failure with hemodialysis sufficed for cure.

M. pachydermatis was the cause of fungemia in a neonatal ICU, affecting 8 premature (gestational age, 23 to 27 weeks) low-birth-weight (600- to 1,000-g) neonates with multiple comorbidities who received total parenteral nutrition with lipid supplementation (58). M. pachydermatis was isolated from blood (6/8 neonates), tracheal aspirate (2/8), eye (1/8) and nose (1/8) secretions, and urine (1/8). The infections were self-limited in 2 neonates, while in the remaining 6 neonates, fungemia was treated with amphotericin B plus flucytosine infusion and fluconazole. The typing of M. pachydermatis strains with PCR-random amplification of polymorphic DNA (PCR-RAPD) (Table 8) generated identical profiles, and an exogenous transfer of the M. pachydermatis strains was supported. Clonal M. pachydermatis and lipophilic Malassezia sp. isolates have been serially isolated from incubator surfaces, supporting the suggestion that M. pachydermatis strains can persist on incubator surfaces for up to 3 months despite standard cleansing procedures. Thus, meticulous personal hygiene of medical and health care staff handling neonates (52) as well as modifications of the cleansing procedures were implemented (319). The potential transfer of M. pachydermatis is highlighted by the fact that DNA has been amplified at high rates from the hands of dog owners regardless of whether the dogs were healthy (92%) or had atopic dermatitis (93%) (225).

Identified risk factors for M. pachydermatis systemic infection include an increased median neonatal acute physiology score, >9 days of arterial catheterization, and contact with a potential carrier (52). The presence of intravascular devices and lipid infusion were not identified as risk factors, suggesting that M. pachydermatis systemic infections do not share a pathogenetic background identical to that of lipophilic Malassezia systemic isolates. The frequency of M. pachydermatis systemic infections was determined retrospectively to be 1.6% in the neonatal ICU (191), and M. pachydermatis was isolated in that same study from CVCs (4/8 neonates); peripheral blood (2/8); urine (4/8); cerebrospinal fluid (1/8); and eye (1/8), ear (1/8), and tracheobronchial (1/8) discharge. M. pachydermatis fungemia in neonates can appear as a cluster of cases (219). In that same study, 28 neonates and 5 adult cases with M. pachydermatis infection were additionally retrospectively identified. The screening of specimens for M. pachydermatis revealed 44/600 (9%) positive samples, whereas for the adult ICU, M. pachydermatis was isolated from only 5 cultures out of 19,000. Eleven lipophilic Malassezia strains were also isolated, but no further data were discussed.

The above-mentioned cases, and additional reported data (192, 210), support the role of M. pachydermatis as a potential pathogen in the neonatal ICU which is capable of generating small-scale epidemics under favorable circumstances, and the diagnosis should not be overlooked when evaluating symptomatic, low-birth-weight, premature infants receiving total parenteral nutrition with lipid supplementation, as simple removal of the catheter after the identification of the causative agent can lead to clinical improvement.

Lipophilic Malassezia species infections.

Lipophilic Malassezia species infections can be divided in two major groups: the first comprising children and adults with various forms of immunosuppression and diverse clinical syndromes and the second involving infants on parenteral nutrition (Table 11). This discrimination was previously described with insight by Redline et al. in 1985 (262). The diagnosed cases comprised an infant group (3 patients) and a second group with ages ranging from 18 months to 48 years (4 patients). The first group included low-birth-weight premature infants (<12 months of age), while the second group incorporated children (>12 months of age) and adults with serious immunosuppression due to gastrointestinal disease. This classification is followed by the majority of reported cases. All patients reported by Redline et al. (262) were receiving TPN with LS (Intralipid; Pharmacia & Upjohn), and as those authors pointed out, linoleic, oleic, and palmitic acids, which are potent growth stimulants of Malassezia species, compose 86% of the TPN-LS infusate. The isolation of the lipophilic Malassezia isolate was achieved by use of standard blood culture media (thioglycolate broth and Trypticase soy broth; Bactec), as minimal growth was supported by small amounts of normally contained lipids. The death of 2 out of 3 infants treated with amphotericin B-flucytosine without a discontinuation of parenteral nutrition underscores the importance of alertness in the clinical laboratory for this potential agent of systemic infection. The poor response to amphotericin B (112), is currently supported by the in vitro-recorded high MIC values of this agent (320). Recent data showed that the M. furfur strains that have the ability to cause systemic infections belong to a distinct internal transcribed spacer 1 group and demonstrate increased phospholipase activity (170).

(i) Malassezia species infections in children and adults.

The first reported Malassezia systemic infection was a case of “sterile peritonitis,” until yeast cells that grew on Sabouraud agar overlaid with olive oil were identified as Pityrosporum ovale (327). Lipids leaking postprandially from the small bowel into the peritoneal cavity were incriminated in the overgrowth of this lipophilic yeast. Continuous ambulatory dialysis is an identified risk factor, and subsequent cases have been described (121, 167, 236). The identification of Malassezia species as a possible agent of infection can lead to the removal of the catheter and resolution of the infection (236). A common characteristic of systemic infections of Malassezia yeasts in adults is the existence of a central venous catheter and total parenteral nutrition (13, 23, 29, 34, 72, 118, 142, 212, 220, 278, 280, 287). Hematologic malignancies (212, 226, 280, 337), cancer (72, 118, 337), and Crohn's disease were the background of Malassezia systemic infections. Also, other less common causes include hyperemesis gravidarum (287), quadriplegia (59), preexisting cellulitis, and sinus formation (236). Apart from the symptoms and signs of systemic infection, clinical syndromes that have been attributed to Malassezia sp. systemic infections include endocardial mass (278), pneumonia (59, 287), osteomyelitis (337), and meningitis (11). Interestingly, some cases have clustered in the spring and summer months (23), and therapy is always assisted by the prompt removal of the central venous catheter. An alternative therapeutic approach that has been proposed is the “locking” of amphotericin B in the catheter (13).

In conclusion, Malassezia sp. systemic infections in adults have variable clinical presentations and can afflict patients with various degrees of immunosuppression. Current data are against their high prevalence, although it is evident that infections caused by this agent, as rare as they may seem, may well be underdiagnosed.

(ii) Malassezia species infections in infants.

The first report of Malassezia fungemia was published in 1981 and described a premature infant (gestational age, 28 weeks; birth weight, 740 g) receiving total parenteral nutrition with lipid supplementation (261). The child developed signs, symptoms, and radiological evidence of pneumonia, with negative bacterial and fungal cultures and without responding to triple-antibacterial chemotherapy. An open-lung biopsy revealed yeast cells, which were erroneously characterized as Candida sp. Infusion with amphotericin B plus flucytosine failed to alleviate symptoms and clear the infection, resulting in death on the 66th hospitalization day. An autopsy reported evidence of small-vessel vasculitis with abundant monopolar budding yeast cells, identified as Malassezia after morphological study in a mycology laboratory. Since then, a plethora of publications describing Malassezia infections in premature and debilitated infants who were receiving total parenteral nutrition with lipid supplementation have been reported (Table 11) (7, 17, 124, 175, 203, 209, 235, 251, 252, 283, 333). As is evident in the cases described in Table 11, the rapid diagnosis and removal of the CVC can suffice for cure when the underlying condition is reversible. An alternative therapeutic approach that has been successfully used incorporates the reallocation of the infusion site to a peripheral vein (209). Malassezia sepsis is not very rare, as it was reported for up to 23% of sepsis cases (3 out of 13 patients) (152) in 263 infants prospectively studied in an ICU and in 2/66 (3%) (291) infants after the placement of a central venous catheter. However, as proper isolation media were not used, only 1 out of 102 identified cases of probable fungemia was attributed to Malassezia (313). The role of health care personnel in the spreading of Malassezia yeasts is significant, as it was incriminated in a miniepidemic during a 7-day period in July 1987 (265). Skin swabs from infants and health care workers revealed that 2 out of 10 infants as well as 2 out of 11 health care workers were colonized. Malassezia systemic infections can be controlled when stringent aseptic care of neonates is enforced (152).

An interesting case of Malassezia yeast central nervous system infection was described after the spread of intravenous administrated fluid to a ruptured dural vein, which was fatal for the neonate (270).

(iii) Systemic infections by lipophilic Malassezia species.

M. sympodialis is rarely reported to be the causative agent of systemic infection (51, 70, 176). M. sympodialis was isolated from the ear lesion of a 53-year-old non-insulin-dependent diabetic man who was receiving intravenous antipseudomonal therapy and was eventually subjected to surgical debridement (51). His condition did not improve but rather deteriorated, with the development of cranial nerve paralysis. Histological examination of tissue specimens obtained from the nasopharynx demonstrated budding yeast cells, and findings suggested a chronic inflammatory reaction. The isolation and identification of M. sympodialis with the subsequent administration of intravenous amphotericin B therapy (1 mg/kg of body weight/day) led to a rapid recovery. The patient was subsequently given fluconazole prophylaxis (400 mg once daily) and was free of clinical and radiological signs of infection 6 months later, although the resulting nerve paralysis did not improve. A central venous catheter-associated M. sympodialis infection in a 63-year-old man receiving total parenteral nutrition with lipids was reported (176). Identification was pursued by Tween utilization tests (Table 1) and sequencing of the internal transcribed spacer 1 region (Table 2). Unfortunately, that strain was not deposited in an international culture collection; thus, it is not available for further virulence studies. A recent epidemiological study identified M. sympodialis catheter colonization in 3 out of 983 intravenous catheters cultured in Dixon's agar (70). In that same study, two more isolates were characterized as being M. furfur (sensu stricto), and 2 isolates did not keep in culture long enough to allow identification to the species level. The only clinical information recorded in that study was that the patients were hospitalized in a surgical ward and were not receiving lipid supplementation. More epidemiological surveys accompanied by detailed laboratory studies would substantiate the potential of M. sympodialis to cause systemic disease.


All observations reported thus far have confirmed the persistence of Malassezia yeasts on incubator surfaces and on the hands of health care workers who are pet dog owners. Therefore, the most important preventive measure against the spread of Malassezia systemic infection in immunocompromised pediatric and adult patient wards entails the scrupulous adherence of medical and health care staff to standard hygienic measures.

The prevention of Malassezia systemic infection by altering the composition of the lipid infusate was suggested by Papavassilis et al. (242). This was based on the observation that medium-chain fatty acids could delay the growth of the seven Malassezia species in vitro, but as the alteration of the infusate composition raises safety issues, clinical trials to determine both safety and efficacy seem imperative. However, the efficiency of this preventive measure has still not been fully explored.


Malassezia isolation followed by identification to the species level should be included in the evaluation of a febrile infant who is receiving total parenteral nutrition with lipid supplementation as well as any patient with immunosuppression and a central venous catheter who presents with persistent fever that is unresponsive to antibiotics and amphotericin B. The seasonal clustering of some reported cases makes this tactic reasonable, especially in ICUs located in countries with a hot and humid climate. Laboratory practices comprising microscopy of blood drawn from the central venous catheter or involved tissue and culture of biological fluids and biopsy specimens in selective medium, as well as an increased incubation time (10 to 15 days), would increase the rate of isolation of lipophilic Malassezia species. However, nonspecific laboratory findings that are commonly found in association with Malassezia systemic infections are leucocytosis or leucocytopenia and thrombocytopenia.

All reported data confirm that an important aspect of Malassezia systemic infections is that they can surface from any background of immunosuppression. Therefore, a high degree of clinical suspicion coupled with laboratory expertise and alertness are prerequisites for the timely management and control of this rare but emerging infection.

Malassezia-Produced AhR Ligands and Significance of AhR Activation on Skin

Malassezia yeasts have the ability to synthesize in vitro an array of indolic compounds when tryptophan is used as the single nitrogen source (108, 157, 158, 336). Within these compounds, some of the most potent ligands of the aryl hydrocarbon receptor (AhR) (synonym, dioxin receptor) have been identified, and, as mentioned above, their quantitative production has been linked to M. furfur strains isolated from cases of seborrheic dermatitis, dandruff, and pityriasis versicolor. AhR is an orphan nuclear receptor, a member of the per-arnt-sim family of proteins, and has pluripotent biological functions in addition to mediating the detrimental effects of dioxin intoxication in the skin and other organs (241). Upon ligand binding, AhR translocates to the nucleus, where it dimerizes with the aryl hydrocarbon nuclear translocator, binds to xenobiotic responsive elements flanking the 5′ ends of genes, and modifies their transcription (155) in a ligand-, cell type-, and tissue-specific manner (96, 253). AhR functions in skin physiology by affecting the cell cycle (182, 260) and melanogenesis (204), while it also modifies responses to injuries, as it affects wound healing (155), mediates UV damage (105), and modifies the inflammatory response to immune signals (22, 174). Among the Malassezia-produced indoles, indirubin is currently proposed to be the endogenous AhR ligand (1, 253).

Indole derivatives isolated from the genus Malassezia.

During the last decade, fungi of the genus Malassezia and especially those of the species M. furfur have been extensively studied for their chemical metabolic profile. When these fungi are cultivated in a selective medium containing tryptophan as the single nitrogen source, they can produce a significant number of chemically diverse indole derivatives (151, 157, 213, 336). A complete list of tryptophan derivatives as Malassezia metabolites that have been isolated up to now is shown in Fig. 7.

Fig 7Fig 7
Chemical structures of the currently identified indoles produced by M. furfur when grown on l-tryptophan agar. The corresponding references of the first description of isolation from Malassezia extracts are in parentheses.

However, despite the significant number of isolated metabolites, only a few of them have been studied for their biological roles.

(i) Malassezin.

Malassezin was initially isolated from ethyl acetate extracts of M. furfur cultures (336). It was found that malassezin induces the apoptosis of melanocytes (184). More specifically, a dose-dependent induction of apoptotic markers after the cultivation of melanocytes with malassezin for 24 h was reported. It was also observed that the biosynthesis of melanin is also reduced in a similar dose-dependent way (184). However, the reduction in the level of melanin is most probably due to the apoptosis of melanocytes, and it is not the result of a specific activity on the biosynthetic pathway of melanin. Nevertheless, the characteristic hypopigmentation associated with pityriasis versicolor has been attributed to this biological action of malassezin. Hypopigmentation seems to be enhanced by the inhibition of melanin transportation from melanocytes to keratinocytes due to the breakdown of the actin cytoskeleton (184).

Additionally, malassezin is an AhR agonist with a 50% effective concentration of (EC50) of 1.57 μΜ, which is able to induce the activity of CYP1A1-dependent 7-deoxyresorufin-Ο-dealkylase (EROD) in hepatocytes (184). However, malassezin does not fulfill the basic structural characteristics that are necessary for AhR agonist activity (336), and for this reason, it is possible that this type of activity could be attributed to the intracellular transformation of malassezin to indolo[3,2-b]carbazole (ICZ) (108, 184).

(ii) ICZ.

ICZ is known as a product of indole-3-carbinol (I3C) condensation in the acidic stomach environment after the ingestion of plants belonging to the genus Brassica (Cruciferae), such as cabbage and broccoli, etc. (248). I3C is a product of glucobrassicin catabolism, a natural ingredient of the above-mentioned foods (188, 336).

ICZ is a highly active agonist of AhR (EC50=2.6 × 10−7 M) (108). It is considered one of the most active, nonhalogenated inducers of AhR ever reported in vitro (248, 330). The affinity of ICZ for AhR is similar to that of dioxin, while it has been found to regulate the expression of AhR-dependent genes in a way similar to that of dioxin (81).

However, in contrast to dioxin, ICZ is metabolically labile, and for this reason, the effects of ICZ are very different from those of dioxin (54). More specifically, experiments with animals have shown that the administration of one dose or repeated doses cannot affect significantly the food intake of experimental animals, in contrast to dioxin. Moreover, after ICZ administration, no growth inhibition or weight reduction was observed, unlike dioxin. Those same studies showed an induction of CYP1A1 in liver (with an increase in levels of mRNA as well as EROD) in animals receiving 127 μg/kg ICZ for 4 days but not as strong as that achieved by dioxin at 5 μg/kg. The induction of CYP1A1 by ICZ is dose dependent, and in contrast to dioxin, the induction is transient due to ICZ metabolism (54).

In addition to CYP1A1, ICZ also affects another protein, breast cancer resistance protein (BCRP), probably through AhR activation. Experiments with Caco-2 cells have shown that ICZ (2.5 μM) can increase significantly the mRNA expression level of BCRP after 8 or 24 h (90). Furthermore, ICZ presented antiestrogenic activity in MCF-7 cells (201).

(iii) Indirubin.

Indirubin and its analogues exhibit inhibitory activities against cell proliferation as well as cytotoxicity and apoptosis induction in human cancer cell lines, and its identification in M. furfur extracts (120) expands the spectrum of the interactions of this yeast with the skin. The interest in indirubin and its derivatives has increased significantly in the last years, after the discovery of its inhibitory activity against cyclin-dependent kinases (CDKs) and glycogen synthase kinase 3 (GSK3). Additionally, indirubin has been found to be one of the most active agonists of the AhR and was also proposed to be the natural ligand of this receptor. In order to clarify the role of kinase inhibition and AhR activation by indirubin in cell proliferation, a study of synthetic derivatives with selective activity proved that AhR activation is responsible for the observed cytostatic effects, while the inhibition of CDKs or GSK3 is responsible for its cytotoxicity (182).

(iv) Pityriacitrin.

Pityriacitrin acts as a strong UV absorbent and most probably is produced by fungal cells as an agent that protects against UV light (206, 215). The presence of pityriacitrin on human skin was initially proposed to convey UV protection to the hypopigmented lesions of pityriasis versicolor and prevent skin from the development of sunburn (190). However, those results were not confirmed by subsequent in vitro experiments (116), and the substances produced by Malassezia yeasts that protect against UV in vivo are still under investigation.

(v) Pityrialactone.

Pityrialactone is also an agent that protects against UV, like pityriacitrin. It is a compound presenting intense yellow-green fluorescence. Its presence in the skin would probably explain the fluorescence observed for pityriasis versicolor skin under Wood lamp fluorescence (216).

(vi) Pityriarubins.

Pityriarubins are bis-indol derivatives with unique structures (158) showing inhibitory activity against the oxidative burst of human granulocytes. Their presence in vivo could explain the absence of inflammation in diseased skin.

(vii) Tryptanthrin.

Tryptanthrin is an alkaloid found in a number of plants, most of them also producing indigo and indirubin. It is a potent inhibitor of prostaglandin and leukotriene synthases in various cell lines and a selective inhibitor of cyclooxygenase 2 (COX-2) (73) and of inducible nitric oxide synthase (iNOS) (NOS II) expression (162). It inhibits the production of IFN-γ and IL-2 after the stimulation of Peyer's patch lymphocytes with staphylococcal enterotoxin B (SEB) (309). Tryptanthrin was also found to inhibit P-glycoprotein (Pgp) through MDR1 gene suppression (346). It was also reported to act as a moderate AhR inducer (281).

(viii) Malassezindole A and keto-malassezin.

Malassezindole A has shown activity in the inhibition of tyrosinase (71) and probably can affect melanin synthesis. Keto-malassezin is also probably a tyrosinase inhibitor capable of inhibiting the dopa reaction on human epidermal melanocytes (71).

Synergy-preferential biosynthesis.

It seems that the synergy between the indole derivatives found in Malassezia can explain some of the clinical symptoms of pityriasis versicolor, like depigmentation (malassezin), resistance to UV light, and reduced inflammatory reactions (pityriarubins) (151, 183).

It should be noted that a number of indole derivatives, like malassezin, ICZ, and indirubin, have been found to be preferentially synthesized by M. furfur strains isolated from seborrheic dermatitis lesions. These compounds are synthesized in significantly higher numbers by strains isolated from diseased skin than by strains isolated from healthy skin (108, 120). These compounds are among the most active known AhR agonists, and this common property implies the possible role of this receptor in the development of Malassezia-related skin diseases.

Malassezia and future research perspectives on skin cancer.

The production of the above-mentioned array of AhR ligands by Malassezia raises the question of a possible participation of this yeast in skin carcinogenesis through the activation of this receptor. Current evidence points toward an association of these yeasts with basal cell carcinoma (115), the malignant tumor with the highest incidence in Caucasians worldwide. Presently, solar UV light is regarded as the most significant carcinogen for this tumor; however, not all basal cell carcinomas are caused by UV light, as these tumors are rare in certain anatomical areas subjected to intense UV radiation exposure throughout life (i.e., dorsal aspects of the hands) and commonly appear on relatively sun-protected skin localizations (i.e., eyelid, inner canthus, and retroauricular area) (145). In the pathogenesis of basal cell carcinomas, activating mutations of the hedgehog pathway at the cellular level are implicated (94, 154), while at the tissue level, they act together with the induction of immune tolerance by the establishing tumor (immunosubversion) (172, 178, 352). The latter is a well-recognized common process in the progression of many types of cancer. Epidemiological observations that indirectly link Malassezia to basal cell carcinoma have come from studies of patients with Parkinson's disease, for whom seborrheic dermatitis and basal cell carcinoma appear at higher rates than expected by a random association despite the reduced prevalence of most other malignancies in this group of patients (102). Additional epidemiological data from different animal species on the rate of Malassezia colonization implied a role for this yeast in the induction of this type of cancer. Malassezia yeasts and basal cell carcinoma are more common in dogs and cats (33), while they are extremely rare in lagomorphs and rodents (325). In dogs and cats, these tumors develop on the head and neck region (272), overlapping with the Malassezia niche in these animals. Furthermore, in dogs, these tumors are more common in hairy animal breeds with long pendulous ears (Saint Bernards and Scottish Terriers), an anatomical trait that promotes Malassezia overgrowth (115). Furthermore, in humans and animals, these tumors and Malassezia yeasts accrue in the so-called seborrheic areas of the face and trunk. Basal cell carcinoma promotion by the Malassezia-synthesized AhR ligands could happen through a modification of UV radiation-induced carcinogenesis, favoring a shift toward the salvage/survival of initiated tumor cells, the inhibition of cell senescence, alterations in vitamin D metabolism, the induction of immune tolerance, and, finally, the procarcinogenic modulation of cell cycle progression and apoptosis (115).


The International Society for Human and Animal Mycology (ISHAM) Malassezia working group continues to promote multidisciplinary global collaborative research.



An external file that holds a picture, illustration, etc.
Object name is zcm9990923720008.jpg

Georgios Gaitanis, M.D., Ph.D., is currently Lecturer at the Department of Skin and Venereal Diseases in the Medical School of Ioannina, Greece. Dr. Gaitanis received his medical degree from the University of Athens Medical School in 1993 and became a Specialist in Dermatology in 2004 in A. Syggros Hospital (Greece). He carried out his Ph.D. work between 1999 and 2003 on Malassezia epidemiology and molecular identification and typing methodology at the Mycology Laboratory, Microbiology Department, Medical School of Athens. He worked as a postdoctoral researcher in the Biology Department of Athens University until he joined the Department of Dermatology at Ioannina Medical School in 2007. All these years, he has been actively involved in Malassezia research, with an interest in epidemiology, genetics, metabolomics, and, lately, the interaction of this yeast with skin cells. The multiple facets of skin interactions with Malassezia would assist in a better understanding of both.


An external file that holds a picture, illustration, etc.
Object name is zcm9990923720009.jpg

Prokopios Magiatis, Ph.D., M.Sc., is assistant Professor of Pharmacognosy and Natural Products Chemistry at the Faculty of Pharmacy of the University of Athens. He graduated from the same Faculty in 1994 and defended his Ph.D. in 2000. In 2001, he did his postdoctoral research at the Curie Institute in Paris, France. He is currently a visiting professor at the University of California, Davis, specializing in the study of the aryl hydrocarbon receptor. In 2009, he was awarded the Egon-Stahl silver medal as the top scientist under 40 years old in the field of natural-products chemistry and pharmacology. His research is focused on the isolation, chemical synthesis, and bioactivity of natural products, especially those reported in ancient medical texts. For the last few years, he has been studying microbial metabolites related to AhR and their relationship with the development of human diseases. He has invented five indirubin derivatives commercially available as pharmacological tools.


An external file that holds a picture, illustration, etc.
Object name is zcm9990923720010.jpg

Markus Hantschke received his medical education from the University of Lübeck and University of California, Los Angeles. He received his M.D. from the University of Lübeck School of Medicine in 1994 and specialized in the field of Dermatology in 1999. During his years as a Dermatology resident, Dr. Hantschke dedicated his main focus to the field of Dermatopathology and also spent a fellowship at the Department of Dermatopathology, University of California, San Francisco, in 2001. In 2002, he joined the partnership of the highly specialized Laboratory for Dermatopathology headquartered in Friedrichshafen, Germany. Dr. Hantschke is an active researcher and has published articles in top-ranked medical journals. His textbook, Dermatopathology, published in 2007 by Steinkopff and in 2011 by Springer, has already been published in a half-dozen languages. In 2008, he was elected General Secretary for the German Society of Dermatopathology (ADH), and he is also active in the International Society of Dermatopathology.


An external file that holds a picture, illustration, etc.
Object name is zcm9990923720011.jpg

Ioannis D. Bassukas, M.D., Ph.D., studied Medicine and specialized in Dermatology-Venereology and Allergiology. He graduated from the University of Athens (Greece) and received his postgraduate degrees from the University of Würzburg (Germany). He joined Brigitte Maurer-Schultze at the Institute of Medical Radiation and Cell Research (University of Würzburg) as a research fellow and worked on the effects of antineoplastic modalities on growth and cell kinetics of normal and malignant tissues. He trained as a resident at the Departments of Pathology (Bonn) and Dermatology (Erlangen) and served as Attending Physician at the Departments of Dermatology, Fachklinik Hornheide University of Münster and University of Lübeck (Germany), and as Vice Director of the Department of Dermatology and Venereology, Academic Hospital Neukölln, Berlin, Germany. He is now Associate Professor of Dermatology and Director of the Department of Skin and Venereal Diseases, University of Ioannina (Greece). His main research interests are skin-focusing human commensal–pathogen interactions and nonsurgical treatment modalities for skin cancer.


An external file that holds a picture, illustration, etc.
Object name is zcm9990923720012.jpg

Aristea Velegraki earned her B.Sc. (honors) and C.N.A.A. in Applied Biology from the University of Sunderland, United Kingdom, and a Ph.D. in Medical Mycology from the Medical School, University of Ioannina, Greece. Her education/training in Medical and Molecular Mycology took place at Service Mycologie, Institut Pasteur, Paris, France; the Department of Medical Microbiology, Medical School, University of Edinburgh, United Kingdom; and the IMI, Surrey, United Kingdom. She was formerly Clinical Scientist, Microbiology Laboratory, Pediatric Hospital P&A, Kyriakou, Athens; Clinical Scientist and Lecturer, Department of Entomology, Parasitology and Tropical Diseases, School of Public Health, Athens, Greece; and Chief Clinical Scientist, Mycology Reference Laboratory, Hellenic Centre for Prevention and Diseases Control, Ministry of Health. Dr. Velegraki is currently Assistant Professor in Mycology, Department of Microbiology, Medical School, National and Kapodistrian University of Athens, Greece, and Curator of the UOA/HCPF929 Culture Collection ( Host-commensal/fungal pathogen interactions, fungal infections, antifungal susceptibility, molecular diagnostics, epidemiology, and metabolomics are research topics on which she has actively published. She was a coeditor of the textbook Malassezia and the Skin (T. Boekhout. E. Gueho, P. Mayser, and A. Velegraki, 2010) and twice elected (2006 to 2012) Vice President of the International Society for Human and Animal Mycology (ISHAM).


1. Adachi J, Mori Y, Matsui S, Matsuda T. 2004. Comparison of gene expression patterns between 2,3,7,8-tetrachlorodibenzo-p-dioxin and a natural arylhydrocarbon receptor ligand, indirubin. Toxicol. Sci. 80:161–169 [PubMed]
2. Agerberth B, et al. 2006. Malassezia sympodialis differently affects the expression of LL-37 in dendritic cells from atopic eczema patients and healthy individuals. Allergy 61:422–430 [PubMed]
3. Aizawa T, Kano R, Nakamura Y, Watanabe S, Hasegawa A. 2001. The genetic diversity of clinical isolates of Malassezia pachydermatis from dogs and cats. Med. Mycol. 39:329–334 [PubMed]
4. Aizawa T, Kano R, Nakamura Y, Watanabe S, Hasegawa A. 1999. Molecular heterogeneity in clinical isolates of Malassezia pachydermatis from dogs. Vet. Microbiol. 70:67–75 [PubMed]
5. Akaza N, et al. 2009. Malassezia folliculitis is caused by cutaneous resident Malassezia species. Med. Mycol. 47:618–624 [PubMed]
6. Akaza N, et al. 2010. Cutaneous Malassezia microbiota in atopic dermatitis patients differ by gender and body part. Dermatology 221:253–260 [PubMed]
7. Alpert G, Bell LM, Campos JM. 1987. Malassezia furfur fungemia in infancy. Clin. Pediatr. (Phila.) 26:528–531 [PubMed]
8. Alves EV, Martins JE, Ribeiro EB, Sotto MN. 2000. Pityrosporum folliculitis: renal transplantation case report. J. Dermatol. 27:49–51 [PubMed]
9. Amaya M, et al. 2007. Molecular analysis of Malassezia microflora in the lesional skin of psoriasis patients. J. Dermatol. 34:619–624 [PubMed]
10. Andersson A, et al. 2004. Cloning, expression and characterization of two new IgE-binding proteins from the yeast Malassezia sympodialis with sequence similarities to heat shock proteins and manganese superoxide dismutase. Eur. J. Biochem. 271:1885–1894 [PubMed]
11. Aoba S, Komiyama A, Hasegawa O. 1993. Fungal meningitis caused by a Malassezia species masquerading as painful ophthalmoplegia. Rinsho Shinkeigaku 33:462–464 [PubMed]
12. Archer-Dubon C, et al. 1999. An epidemic outbreak of Malassezia folliculitis in three adult patients in an intensive care unit: a previously unrecognized nosocomial infection. Int. J. Dermatol. 38:453–456 [PubMed]
13. Arnow PM, Kushner R. 1991. Malassezia furfur catheter infection cured with antibiotic lock therapy. Am. J. Med. 90:128–130 [PubMed]
14. Ashbee HR, Evans EG. 2002. Immunology of diseases associated with Malassezia species. Clin. Microbiol. Rev. 15:21–57 [PMC free article] [PubMed]
15. Atherton DJ, Gennery AR, Cant AJ. 2004. The neonate, p 1422–1429 In Burns T, Breathnach S, Cox N, Griffiths C, editors. (ed), Rooks textbook of dermatology, 7th ed. Blackwell Publishing, Oxford, United Kingdom
16. Ayers K, Sweeney SM, Wiss K. 2005. Pityrosporum folliculitis: diagnosis and management in 6 female adolescents with acne vulgaris. Arch. Pediatr. Adolesc. Med. 159:64–67 [PubMed]
17. Azimi PH, et al. 1988. Malassezia furfur: a cause of occlusion of percutaneous central venous catheters in infants in the intensive care nursery. Pediatr. Infect. Dis. J. 7:100–103 [PubMed]
18. Bäck O, Faergemann J, Hörnqvist R. 1985. Pityrosporum folliculitis: a common disease of the young and middle-aged. J. Am. Acad. Dermatol. 12:56–61 [PubMed]
19. Baillon H. 1889. Traité de botanique médicale cryptogamique, paris, 4th ed Octave Doin, Paris, France
20. Balaji H, et al. 2011. Malassezia sympodialis thioredoxin-specific T cells are highly cross-reactive to human thioredoxin in atopic dermatitis. J. Allergy Clin. Immunol. 128:92–99 [PubMed]
21. Bamford JT. 1983. Treatment of tinea versicolor with sulfur-salicylic shampoo. J. Am. Acad. Dermatol. 8:211–213 [PubMed]
22. Bankoti J, Rase B, Simones T, Shepherd DM. 2010. Functional and phenotypic effects of AhR activation in inflammatory dendritic cells. Toxicol. Appl. Pharmacol. 246:18–28 [PMC free article] [PubMed]
23. Barber GR, Brown AE, Kiehn TE, Edwards FF, Armstrong D. 1993. Catheter-related Malassezia furfur fungemia in immunocompromised patients. Am. J. Med. 95:365–370 [PubMed]
24. Barchmann T, Hort W, Krämer HJ, Mayser P. 2011. Glycine as a regulator of tryptophan-dependent pigment synthesis in Malassezia furfur. Mycoses 54:17–22 [PubMed]
25. Barfatani M, Munn RJ, Schjeide OA. 1964. An ultrastructure study of Pityrosporum orbiculare. J. Invest. Dermatol. 43:231–233 [PubMed]
26. Baroni A, et al. 2006. Toll-like receptor 2 (TLR2) mediates intracellular signalling in human keratinocytes in response to Malassezia furfur. Arch. Dermatol. Res. 297:280–288 [PubMed]
27. Baroni A, et al. 2004. Possible role of Malassezia furfur in psoriasis: modulation of TGF-beta1, integrin, and HSP70 expression in human keratinocytes and in the skin of psoriasis-affected patients. J. Cutan. Pathol. 31:35–42 [PubMed]
28. Baroni A, et al. 2001. Malassezia furfur invasiveness in a keratinocyte cell line (HaCat): effects on cytoskeleton and on adhesion molecule and cytokine expression. Arch. Dermatol. Res. 293:414–419 [PubMed]
29. Bhargava P, Longhi LP. 2007. Images in clinical medicine. Peripheral smear with Malassezia furfur. N. Engl. J. Med. 356:e25. [PubMed]
30. Bieber T. 2008. Atopic dermatitis. N. Engl. J. Med. 358:1483–1494 [PubMed]
31. Binder RL, Jonelis FJ. 1983. Seborrheic dermatitis in neuroleptic-induced Parkinsonism. Arch. Dermatol. 119:473–475 [PubMed]
32. Bizzozero J. 1884. Über die Mykrophyten der normalen Oberhaut des Menschen. Virchows Arch. Pathol. Anat. Physiol. 98:441–459
33. Bond R, Cabañes GJJ. 2010. Malassezia yeasts in animal disease, p 271–300. In Boekhout T, Guého E, Mayser P, Velegraki A, editors. (ed), Malassezia and the skin. Science and clinical practice. Springer, Berlin, Germany:
34. Brooks R, Brown L. 1987. Systemic infection with Malassezia furfur in an adult receiving long-term hyperalimentation therapy. J. Infect. Dis. 156:410–411 [PubMed]
35. Brunke S, Hube B. 2006. MfLIP1, a gene encoding an extracellular lipase of the lipid-dependent fungus Malassezia furfur. Microbiology 152:547–554 [PubMed]
36. Bulmer GS, Pu XM, Yi LX. 2008. Malassezia folliculitis in China. Mycopathologia 165:411–412 [PubMed]
37. Burton JL, Pye RJ. 1983. Seborrhoea is not a feature of seborrhoeic dermatitis. Br. Med. J. (Clin. Res. Ed.) 286:1169–1170 [PMC free article] [PubMed]
38. Cabanes FJ, Hernandez JJ, Castella G. 2005. Molecular analysis of Malassezia sympodialis-related strains from domestic animals. J. Clin. Microbiol. 43:277–283 [PMC free article] [PubMed]
39. Cabanes FJ, Theelen B, Castella G, Boekhout T. 2007. Two new lipid-dependent Malassezia species from domestic animals. FEMS Yeast Res. 7:1064–1076 [PubMed]
40. Cabanes FJ, Vega S, Castella G. 2011. Malassezia cuniculi sp. nov., a novel yeast species isolated from rabbit skin. Med. Mycol. 49:40–48 [PubMed]
41. Cafarchia C, Dell'Aquila ME, Capelli G, Minoia P, Otranto D. 2007. Role of beta-endorphin on phospholipase production in Malassezia pachydermatis in dogs: new insights into the pathogenesis of this yeast. Med. Mycol. 45:11–15 [PubMed]
42. Cafarchia C, et al. 2010. Expression of the micro-opioid receptor on Malassezia pachydermatis and its effect in modulating phospholipase production. Med. Mycol. 48:73–78 [PubMed]
43. Cafarchia C, et al. 2008. Genetic variants of Malassezia pachydermatis from canine skin: body distribution and phospholipase activity. FEMS Yeast Res. 8:451–459 [PubMed]
44. Cafarchia C, Otranto D. 2004. Association between phospholipase production by Malassezia pachydermatis and skin lesions. J. Clin. Microbiol. 42:4868–4869 [PMC free article] [PubMed]
45. Cafarchia C, et al. 2007. Multilocus mutation scanning for the analysis of genetic variation within Malassezia (Basidiomycota: Malasseziales). Electrophoresis 28:1176–1180 [PubMed]
46. Cafarchia C, et al. 2007. Molecular characterization of Malassezia isolates from dogs using three distinct genetic markers in nuclear DNA. Mol. Cell. Probes 21:229–238 [PubMed]
47. Canteros CE, et al. 2007. Concordance between phenotypical features and PCR-REA for the identification of Malassezia spp. Rev. Iberoam. Micol. 24:278–282 [PubMed]
48. Casagrande BF, et al. 2006. Sensitization to the yeast Malassezia sympodialis is specific for extrinsic and intrinsic atopic eczema. J. Invest. Dermatol. 126:2414–2421 [PubMed]
49. Castella G, Hernandez JJ, Cabanes FJ. 2005. Genetic typing of Malassezia pachydermatis from different domestic animals. Vet. Microbiol. 108:291–296 [PubMed]
50. Castellani A, Chalmers AJ. 1913. Manual of tropical medicine, 2nd ed. Baillière, Tindal, and Cox, London, United Kingdom
51. Chai FC, Auret K, Christiansen K, Yuen PW, Gardam D. 2000. Malignant otitis externa caused by Malassezia sympodialis. Head Neck 22:87–89 [PubMed]
52. Chang HJ, et al. 1998. An epidemic of Malassezia pachydermatis in an intensive care nursery associated with colonization of health care workers' pet dogs. N. Engl. J. Med. 338:706–711 [PubMed]
53. Chaudhary R, Singh S, Banerjee T, Tilak R. 2010. Prevalence of different Malassezia species in pityriasis versicolor in central India. Indian J. Dermatol. Venereol. Leprol. 76:159–164 [PubMed]
54. Chen YH, et al. 1995. Regulation of CYP1A1 by indolo[3,2-b]carbazole in murine hepatoma cells. J. Biol. Chem. 270:22548–22555 [PubMed]
55. Chetty GN, Kamalam A, Thambiah AS. 1979. Pityriasis versicolor—a study of 200 cases in a tropical skin clinic. Mykosen 22:234–236 [PubMed]
56. Cholongitas E, Pipili C, Ioannidou D. 2009. Malassezia folliculitis presented as acneiform eruption after cetuximab administration. J. Drugs Dermatol. 8:274–275 [PubMed]
57. Chowdhary A, Randhawa HS, Sharma S, Brandt ME, Kumar S. 2005. Malassezia furfur in a case of onychomycosis: colonizer or etiologic agent? Med. Mycol. 43:87–90 [PubMed]
58. Chryssanthou E, Broberger U, Petrini B. 2001. Malassezia pachydermatis fungaemia in a neonatal intensive care unit. Acta Paediatr. 90:323–327 [PubMed]
59. Chu CM, Lai RW. 2002. Malassezia furfur fungaemia in a ventilator-dependent patient without known risk factors. Hong Kong Med. J. 8:212–214 [PubMed]
60. Cork MJ, et al. 2009. Epidermal barrier dysfunction in atopic dermatitis. J. Invest. Dermatol. 129:1892–1908 [PubMed]
61. Cotterill JA, Cunliffe WJ, Williamson B, Bulusu L. 1972. Age and sex variation in skin surface lipid composition and sebum excretion rate. Br. J. Dermatol. 87:333–340 [PubMed]
62. Coutinho SD, Paula CR. 2000. Proteinase, phospholipase, hyaluronidase and chondroitin-sulphatase production by Malassezia pachydermatis. Med. Mycol. 38:73–76 [PubMed]
63. Crespo Erchiga V, Ojeda Martos A, Vera Casano A, Crespo Erchiga A, Sanchez Fajardo F. 2000. Malassezia globosa as the causative agent of pityriasis versicolor. Br. J. Dermatol. 143:799–803 [PubMed]
64. Crespo Erchiga V, Ojeda Martos AA, Vera Casano A, Crespo Erchiga A, Sanchez Fajardo F. 1999. Isolation and identification of Malassezia spp. in pytiriasis versicolor, seborrheic dermatitis and healthy skin. Rev. Iberoam. Micol. 16:S16–S21 [PubMed]
65. Crespo Erchiga V, Hay RJ. 2010. Pityriasis versicolor and other Malassezia skin diseases, p 175–199 In Boekhout T, Guého E, Mayser P, Velegraki A, editors. (ed), Malassezia and the skin. Science and clinical practice. Springer, Berlin, Germany
66. Crowson AN, Magro CM. 2003. Atrophying tinea versicolor: a clinical and histological study of 12 patients. Int. J. Dermatol. 42:928–932 [PubMed]
67. Crozier WJ, Wise KA. 1993. Onychomycosis due to Pityrosporum. Australas. J. Dermatol. 34:109–112 [PubMed]
68. Cuetara MS, Aguilar A, Martin L, Aspiroz C, del Palacio A. 2006. Erlotinib associated with rosacea-like folliculitis and Malassezia sympodialis. Br. J. Dermatol. 155:477–479 [PubMed]
69. Cunningham AC, Leeming JP, Ingham E, Gowland G. 1990. Differentiation of three serovars of Malassezia furfur. J. Appl. Bacteriol. 68:439–446 [PubMed]
70. Curvale-Fauchet N, Botterel F, Legrand P, Guillot J, Bretagne S. 2004. Frequency of intravascular catheter colonization by Malassezia spp. in adult patients. Mycoses 47:491–494 [PubMed]
71. Dahms K, Krämer H-J, Thoma W, Mayser P. 2002. Tyrosinaseinhibition durch Tryptophanmetabolite von Malassezia furfur in humaner Epidermis. Mycoses 45:230
72. Dankner WM, Spector SA, Fierer J, Davis CE. 1987. Malassezia fungemia in neonates and adults: complication of hyperalimentation. Rev. Infect. Dis. 9:743–753 [PubMed]
73. Danz H, Stoyanova S, Wippich P, Brattstrom A, Hamburger M. 2001. Identification and isolation of the cyclooxygenase-2 inhibitory principle in Isatis tinctoria. Planta Med. 67:411–416 [PubMed]
74. Dawson TL., Jr 2007. Malassezia globosa and restricta: breakthrough understanding of the etiology and treatment of dandruff and seborrheic dermatitis through whole-genome analysis. J. Invest. Dermatol. Symp. Proc. 12:15–19 [PubMed]
75. DeAngelis YM, et al. 2005. Three etiologic facets of dandruff and seborrheic dermatitis: Malassezia fungi, sebaceous lipids, and individual sensitivity. J. Invest. Dermatol. Symp. Proc. 10:295–297 [PubMed]
76. DeAngelis YM, et al. 2007. Isolation and expression of a Malassezia globosa lipase gene, LIP1. J. Invest. Dermatol. 127:2138–2146 [PubMed]
77. De Benedetto A, Agnihothri R, McGirt LY, Bankova LG, Beck LA. 2009. Atopic dermatitis: a disease caused by innate immune defects? J. Invest. Dermatol. 129:14–30 [PubMed]
78. Dehghan M, Akbari N, Alborzi N, Sadani S, Keshtkar AA. 2010. Single-dose oral fluconazole versus topical clotrimazole in patients with pityriasis versicolor: a double-blind randomized controlled trial. J. Dermatol. 37:699–702 [PubMed]
79. De Jong MA, et al. 2010. C-type lectin Langerin is a beta-glucan receptor on human Langerhans cells that recognizes opportunistic and pathogenic fungi. Mol. Immunol. 47:1216–1225 [PMC free article] [PubMed]
80. De Luca C, Picardo M, Breathnach A, Passi S. 1996. Lipoperoxidase activity of Pityrosporum: characterisation of by-products and possible role in pityriasis versicolor. Exp. Dermatol. 5:49–56 [PubMed]
81. De Waard PW, et al. 2008. A human intervention study with foods containing natural Ah-receptor agonists does not significantly show AhR-mediated effects as measured in blood cells and urine. Chem. Biol. Interact. 176:19–29 [PubMed]
82. Diaz MR, et al. 2006. Microcoding and flow cytometry as a high-throughput fungal identification system for Malassezia species. J. Med. Microbiol. 55:1197–1209 [PubMed]
83. Difonzo EM, Faggi E. 2008. Skin diseases associated with Malassezia species in humans. Clinical features and diagnostic criteria. Parassitologia 50:69–71 [PubMed]
84. Di Silverio A, Zeccara C, Serra F, Ubezio S, Mosca M. 1995. Pityriasis versicolor in a newborn. Mycoses 38:227–228 [PubMed]
85. Di Silverio A, Mosca M, Brandozzi G, Gatti M. 1989. Pityriasis versicolor in the aged: a clinical investigation and epidemiological survey in 190 elderly hospitalized patients. Mycopathologia 105:187–190 [PubMed]
86. Donnarumma G, et al. 2004. Malassezia furfur induces the expression of beta-defensin-2 in human keratinocytes in a protein kinase C-dependent manner. Arch. Dermatol. Res. 295:474–481 [PubMed]
87. Dorn M, Roehnert K. 1977. Dimorphism of Pityrosporum orbiculare in a defined culture medium. J. Invest. Dermatol. 69:244–248 [PubMed]
88. Duarte ER, Hamdan JS. 2010. RAPD differentiation of Malassezia spp. from cattle, dogs and humans. Mycoses 53:48–56 [PubMed]
89. Dutta S, Bajaj AK, Basu S, Dikshit A. 2002. Pityriasis versicolor: socioeconomic and clinico-mycologic study in India. Int. J. Dermatol. 41:823–824 [PubMed]
90. Ebert B, Seidel A, Lampen A. 2005. Identification of BCRP as transporter of benzo[a]pyrene conjugates metabolically formed in Caco-2 cells and its induction by Ah-receptor agonists. Carcinogenesis 26:1754–1763 [PubMed]
91. Eichstedt E. 1846. Pilzbildung in der Pityriasis versicolor. Froriep. Neue Notiz. Natur. Heilk. 39:270
92. Elewski B. 1990. Does pityrosporum ovale have a role in psoriasis? Arch. Dermatol. 126:1111–1112 [PubMed]
93. el-Hefnawi H, el-Gothamy Z, Refai M. 1971. Studies on pityriasis versicolor in Egypt. I. Incidence. Mykosen 14:225–231 [PubMed]
94. Epstein EH. 2008. Basal cell carcinomas: attack of the hedgehog. Nat. Rev. Cancer 8:743–754 [PubMed]
95. Ertam I, Aytimur D, Alper S. 2007. Malassezia furfur onychomycosis in an immunosuppressed liver transplant recipient. Indian J. Dermatol. Venereol. Leprol. 73:425–426 [PubMed]
96. Esser C, Rannug A, Stockinger B. 2009. The aryl hydrocarbon receptor in immunity. Trends Immunol. 30:447–454 [PubMed]
97. Faergemann J. 1992. Pityrosporum infections, p 69–83 In Elewski BE, editor. (ed), Cutaneous fungal infections. Igaku-Shoin, New York, NY
98. Faergemann J, Bergbrant IM, Dohse M, Scott A, Westgate G. 2001. Seborrhoeic dermatitis and Pityrosporum (Malassezia) folliculitis: characterization of inflammatory cells and mediators in the skin by immunohistochemistry. Br. J. Dermatol. 144:549–556 [PubMed]
99. Faergemann J, Johansson S, Bäck O, Scheynius A. 1986. An immunologic and cultural study of Pityrosporum folliculitis. J. Am. Acad. Dermatol. 14:429–433 [PubMed]
100. Faergemann J, et al. 2009. A double-blind, randomized, placebo-controlled, dose-finding study of oral pramiconazole in the treatment of pityriasis versicolor. J. Am. Acad. Dermatol. 61:971–976 [PubMed]
101. Farr PM, Krause LB, Marks JM, Shuster S. 1985. Response of scalp psoriasis to oral ketoconazole. Lancet ii:921–922 [PubMed]
102. Ferreira J, et al. 2007. Skin cancers and precancerous lesions in Parkinson's disease patients. Mov. Disord. 22:1471–1475 [PubMed]
103. Fine RN, et al. 1983. Peritonitis in children undergoing continuous ambulatory peritoneal dialysis. Pediatrics 71:806–809 [PubMed]
104. Fredriksson T, Faergemann J. 1983. Double-blind comparison of a zinc pyrithione shampoo and its shampoo base in the treatment of tinea versicolor. Cutis 31:436–437 [PubMed]
105. Fritsche E, et al. 2007. Lightening up the UV response by identification of the arylhydrocarbon receptor as a cytoplasmatic target for ultraviolet B radiation. Proc. Natl. Acad. Sci. U. S. A. 104:8851–8856 [PubMed]
106. Gaitanis G, Bassukas ID, Velegraki A. 2009. The range of molecular methods for typing Malassezia. Curr. Opin. Infect. Dis. 22:119–225 [PubMed]
107. Gaitanis G, Chasapi V, Velegraki A. 2005. Novel application of the Masson-Fontana stain for demonstrating Malassezia species melanin-like pigment production in vitro and in clinical specimens. J. Clin. Microbiol. 43:4147–4151 [PMC free article] [PubMed]
108. Gaitanis G, et al. 2008. AhR ligands, malassezin, and indolo[3,2-b]carbazole are selectively produced by Malassezia furfur strains isolated from seborrheic dermatitis. J. Invest. Dermatol. 128:1620–1625 [PubMed]
109. Gaitanis G, Menounos P, Katsambas A, Velegraki A. 2003. Detection and mutation screening of Malassezia sympodialis sequences coding for the Mal s 1 allergen implicated in atopic dermatitis. J. Invest. Dermatol. 121:1559–1560 [PubMed]
110. Gaitanis G, Mayser P, Scheynius A, Crameri R. 2010. Malassezia yeasts in seborrheic and atopic eczemas, p 201–228 In Boekhout T, Guého E, Mayser P, Velegraki A, editors. (ed), Malassezia and the skin. Science and clinical practice. Springer, Berlin, Germany
111. Gaitanis G, Robert V, Velegraki A. 2006. Verifiable single nucleotide polymorphisms of the internal transcribed spacer 2 region for the identification of 11 Malassezia species. J. Dermatol. Sci. 43:214–217 [PubMed]
112. Gaitanis G, et al. 2006. Distribution of Malassezia species in pityriasis versicolor and seborrhoeic dermatitis in Greece. Typing of the major pityriasis versicolor isolate M. globosa. Br. J. Dermatol. 154:854–859 [PubMed]
113. Gaitanis G, et al. 2009. Malassezia furfur fingerprints as possible markers for human phylogeography. ISME J. 3:498–502 [PubMed]
114. Gaitanis G, et al. 2002. Identification of Malassezia species from patient skin scales by PCR-RFLP. Clin. Microbiol. Infect. 8:162–173 [PubMed]
115. Gaitanis G, Velegraki A, Magiatis P, Pappas P, Bassukas ID. 2011. Could Malassezia yeasts be implicated in skin carcinogenesis through the production of aryl-hydrocarbon receptor ligands? Med. Hypotheses 77:47–51 [PubMed]
116. Gambichler T, et al. 2007. Quantification of ultraviolet protective effects of pityriacitrin in humans. Arch. Dermatol. Res. 299:517–520 [PubMed]
117. Gandra RF, et al. 2006. Genotyping by RAPD-PCR analyses of Malassezia furfur strains from pityriasis versicolor and seborrhoeic dermatitis patients. Mycopathologia 162:273–280 [PubMed]
118. Garcia CR, Johnston BL, Corvi G, Walker LJ, George WL. 1987. Intravenous catheter-associated Malassezia furfur fungemia. Am. J. Med. 83:790–792 [PubMed]
119. Gemmer CM, DeAngelis YM, Theelen B, Boekhout T, Dawson TL., Jr 2002. Fast, noninvasive method for molecular detection and differentiation of Malassezia yeast species on human skin and application of the method to dandruff microbiology. J. Clin. Microbiol. 40:3350–3357 [PMC free article] [PubMed]
120. Giakoumaki D, et al. 2008. Identification of indirubin as a metabolite of Malassezia furfur strains isolated from diseased skin. Planta Med. 74:1081
121. Gidding H, Hawes L, Dwyer B. 1989. The isolation of Malassezia furfur from an episode of peritonitis. Med. J. Aust. 151:603. [PubMed]
122. Giusiano G, de los Angeles Sosa M, Rojas F, Vanacore ST, Mangiaterra M. 2010. Prevalence of Malassezia species in pityriasis versicolor lesions in northeast Argentina. Rev. Iberoam. Micol. 27:71–74 [PubMed]
123. Glaser AG, et al. 2006. Analysis of the cross-reactivity and of the 1.5 A crystal structure of the Malassezia sympodialis Mala s 6 allergen, a member of the cyclophilin pan-allergen family. Biochem. J. 396:41–49 [PubMed]
124. Glaser CA, Atwater SK. 1995. Febrile infant with a percutaneous vascular catheter. Pediatr. Infect. Dis. J. 14:163, 165–166 [PubMed]
125. Gonzalez A, et al. 2009. Physiological and molecular characterization of atypical isolates of Malassezia furfur. J. Clin. Microbiol. 47:48–53 [PMC free article] [PubMed]
126. Goodfield MJ, Saihan EM, Crowley J. 1987. Experimental folliculitis with Pityrosporum orbiculare: the influence of host response. Acta Derm. Venereol. 67:445–447 [PubMed]
127. Gordon MA. 1951. The lipophilic mycoflora of the skin. 1. In vitro culture of Pityrosporum orbiculare n. sp. Mycologia 43:524–535
128. Graham LM, Brown GD. 2009. The dectin-2 family of C-type lectins in immunity and homeostasis. Cytokine 48:148–155 [PMC free article] [PubMed]
129. Guého E, Midgley G, Guillot J. 1996. The genus Malassezia with description of four new species. Antonie Van Leeuwenhoek 69:337–355 [PubMed]
130. Guillot J, Deville M, Berthelemy M, Provost F, Guého E. 2000. A single PCR-restriction endonuclease analysis for rapid identification of Malassezia species. Lett. Appl. Microbiol. 31:400–403 [PubMed]
131. Guillot J, Guého E. 1995. The diversity of Malassezia yeasts confirmed by rRNA sequence and nuclear DNA comparisons. Antonie Van Leeuwenhoek 67:297–314 [PubMed]
132. Guillot J, Lesourd EGM, Midgley G, Chévrier G, Dupont B. 1996. Identification of Malassezia species: a practical approach. J. Mycol. Med. 6:103–110
133. Gupta AK, Batra R, Bluhm R, Boekhout T, Dawson TL., Jr 2004. Skin diseases associated with Malassezia species. J. Am. Acad. Dermatol. 51:785–798 [PubMed]
134. Gupta AK, Boekhout T, Theelen B, Summerbell R, Batra R. 2004. Identification and typing of Malassezia species by amplified fragment length polymorphism and sequence analyses of the internal transcribed spacer and large-subunit regions of ribosomal DNA. J. Clin. Microbiol. 42:4253–4260 [PMC free article] [PubMed]
135. Gupta AK, Kohli Y. 2004. Prevalence of Malassezia species on various body sites in clinically healthy subjects representing different age groups. Med. Mycol. 42:35–42 [PubMed]
136. Gupta AK, Kohli Y, Faergemann J, Summerbell RC. 2001. Epidemiology of Malassezia yeasts associated with pityriasis versicolor in Ontario, Canada. Med. Mycol. 39:199–206 [PubMed]
137. Gupta AK, Kohli Y, Li A, Faergemann J, Summerbell RC. 2000. In vitro susceptibility of the seven Malassezia species to ketoconazole, voriconazole, itraconazole and terbinafine. Br. J. Dermatol. 142:758–765 [PubMed]
138. Gupta AK, Kohli Y, Summerbell RC, Faergemann J. 2001. Quantitative culture of Malassezia species from different body sites of individuals with or without dermatoses. Med. Mycol. 39:243–251 [PubMed]
139. Gustafsson BA. 1955. Otitis externa in the dog. A bacteriological and experimental study. Ph.D. thesis. Royal Veterinary College, Stockholm, Sweden
140. Hafez M, el-Shamy S. 1985. Genetic susceptibility in pityriasis versicolor. Dermatologica 171:86–88 [PubMed]
141. Han A, et al. 2009. Evoked scale sign of tinea versicolor. Arch. Dermatol. 145:1078. [PubMed]
142. Hassall E, Ulich T, Ament ME. 1983. Pulmonary embolus and Malassezia pulmonary infection related to urokinase therapy. J. Pediatr. 102:722–725 [PubMed]
143. Hazen KC. 1995. New and emerging yeast pathogens. Clin. Microbiol. Rev. 8:462–478 [PMC free article] [PubMed]
144. He SM, et al. 2008. The genetic epidemiology of tinea versicolor in China. Mycoses 51:55–62 [PubMed]
145. Heckmann M, Zogelmeier F, Konz B. 2002. Frequency of facial basal cell carcinoma does not correlate with site-specific UV exposure. Arch. Dermatol. 138:1494–1497 [PubMed]
146. Hedayati MT, et al. 2010. Identification of Malassezia species isolated from Iranian seborrhoeic dermatitis patients. Eur. Rev. Med. Pharmacol. Sci. 14:63–68 [PubMed]
147. Hellgren L, Vincent J. 1983. The incidence of tinea versicolor in central Sweden. J. Med. Microbiol. 16:501–502 [PubMed]
148. Hier SW, Cornbleet T, Bergeim O. 1946. The amino acids of human sweat. J. Biol. Chem. 166:327–333 [PubMed]
149. Hill MK, Goodfield MJ, Rodgers FG, Crowley JL, Saihan EM. 1990. Skin surface electron microscopy in Pityrosporum folliculitis. The role of follicular occlusion in disease and the response to oral ketoconazole. Arch. Dermatol. 126:1071–1074 [PubMed]
150. Hirai A, et al. 2004. Malassezia nana sp. nov., a novel lipid-dependent yeast species isolated from animals. Int. J. Syst. Evol. Microbiol. 54:623–627 [PubMed]
151. Hort W, Mayser P. 2011. Malassezia virulence determinants. Curr. Opin. Infect. Dis. 24:100–105 [PubMed]
152. Hruszkewycz V, et al. 1991. Complications associated with central venous catheters inserted in critically ill neonates. Infect. Control Hosp. Epidemiol. 12:544–548 [PubMed]
153. Hu SW, Bigby M. 2010. Pityriasis versicolor: a systematic review of interventions. Arch. Dermatol. 146:1132–1140 [PubMed]
154. Hutchin ME, et al. 2005. Sustained Hedgehog signaling is required for basal cell carcinoma proliferation and survival: conditional skin tumorigenesis recapitulates the hair growth cycle. Genes Dev. 19:214–223 [PubMed]
155. Ikuta T, Namiki T, Fujii-Kuriyama Y, Kawajiri K. 2009. AhR protein trafficking and function in the skin. Biochem. Pharmacol. 77:588–596 [PubMed]
156. Ingordo V, Naldi L, Colecchia B, Licci N. 2003. Prevalence of pityriasis versicolor in young Italian sailors. Br. J. Dermatol. 149:1270–1272 [PubMed]
157. Irlinger B, Bartsch A, Krämer HJ, Mayser P, Steglich W. 2005. New tryptophan metabolites from cultures of the lipophilic yeast Malassezia furfur. Helv. Chim. Acta 88:1472–1485
158. Irlinger B, Krämer HJ, Mayser P, Steglich W. 2004. Pityriarubins, biologically active bis(indolyl)spirans from cultures of the lipophilic yeast Malassezia furfur. Angew. Chem. Int. Ed. Engl. 43:1098–1100 [PubMed]
159. Ishibashi Y, Kato H, Asahi Y, Sugita T, Nishikawa A. 2009. Identification of the major allergen of Malassezia globosa relevant for atopic dermatitis. J. Dermatol. Sci. 55:185–192 [PubMed]
160. Ishibashi Y, Sugawara K, Sugita T, Nishikawa A. 2011. Secretion of thymic stromal lymphopoietin from human keratinocytes in response to Malassezia yeasts. J. Dermatol. Sci. 62:134–138 [PubMed]
161. Ishibashi Y, Sugita T, Nishikawa A. 2006. Cytokine secretion profile of human keratinocytes exposed to Malassezia yeasts. FEMS Immunol. Med. Microbiol. 48:400–409 [PubMed]
162. Ishihara T, et al. 2000. Tryptanthrin inhibits nitric oxide and prostaglandin E(2) synthesis by murine macrophages. Eur. J. Pharmacol. 407:197–204 [PubMed]
163. Jacinto-Jamora S, Tamesis J, Katigbak ML. 1991. Pityrosporum folliculitis in the Philippines: diagnosis, prevalence, and management. J. Am. Acad. Dermatol. 24:693–696 [PubMed]
164. Jang SJ, et al. 2009. The investigation on the distribution of Malassezia yeasts on the normal Korean skin by 26S rDNA PCR-RFLP. Ann. Dermatol. 21:18–26 [PMC free article] [PubMed]
165. Jing W, Ismail R. 1999. Mucocutaneous manifestations of HIV infection: a retrospective analysis of 145 cases in a Chinese population in Malaysia. Int. J. Dermatol. 38:457–463 [PubMed]
166. Johansson SG, et al. 2004. Revised nomenclature for allergy for global use: report of the Nomenclature Review Committee of the World Allergy Organization, October 2003. J. Allergy Clin. Immunol. 113:832–836 [PubMed]
167. Johnson AS, Bailey E, Wright PA, Solomon L. 1996. Malassezia furfur: a possible cause of culture-negative CAPD peritonitis. Perit. Dial. Int. 16:187–188 [PubMed]
168. Jowkar F, Jamshidzadeh A, Pakniyat S, Namazi MR. 2010. Efficacy of nitric oxide-liberating cream on pityriasis versicolor. J. Dermatolog. Treat. 21:93–96 [PubMed]
169. Ju Q, et al. 2011. 2,3,7,8-Tetrachlorodibenzo-p-dioxin alters sebaceous gland cell differentiation in vitro. Exp. Dermatol. 20:320–325 [PubMed]
170. Kaneko T, Murotani M, Ohkusu K, Sugita T, Makimura K. Genetic and biological features of catheter-associated Malassezia furfur. Med. Mycol., in press [PubMed]
171. Kaneko T, et al. 2010. Human external ear canal as the specific reservoir of Malassezia slooffiae. Med. Mycol. 48:824–827 [PubMed]
172. Kaporis HG, et al. 2007. Human basal cell carcinoma is associated with Foxp3+ T cells in a Th2 dominant microenvironment. J. Invest. Dermatol. 127:2391–2398 [PubMed]
173. Karakaş M, Turaç-Biçer A, Ilkit M, Durdu M, Seydaoğlu G. 2009. Epidemiology of pityriasis versicolor in Adana, Turkey. J. Dermatol. 36:377–382 [PubMed]
174. Kerkvliet NI. 2009. AHR-mediated immunomodulation: the role of altered gene transcription. Biochem. Pharmacol. 77:746–760 [PMC free article] [PubMed]
175. Kessler AT, Kourtis AP, Simon N. 2002. Peripheral thromboembolism associated with Malassezia furfur sepsis. Pediatr. Infect. Dis. J. 21:356–357 [PubMed]
176. Kikuchi K, et al. 2001. A case of central venous catheter-related infection with Malassezia sympodialis. Nippon Ishinkin Gakkai Zasshi 42:220–222 (In Japanese.) [PubMed]
177. Kim D, Lim YR, Ohk SO, Kim BJ, Chun YJ. 2011. Functional expression and characterization of CYP51 from dandruff-causing Malassezia globosa. FEMS Yeast Res. 11:80–87 [PubMed]
178. Kim J, et al. 1995. IL-10 production in cutaneous basal and squamous cell carcinomas. A mechanism for evading the local T cell immune response. J. Immunol. 155:2240–2247 [PubMed]
179. Kim YJ, Kim YC. 2007. Successful treatment of pityriasis versicolor with 5-aminolevulinic acid photodynamic therapy. Arch. Dermatol. 143:1218–1220 [PubMed]
180. Kindo AJ, Sophia SK, Kalyani J, Anandan S. 2004. Identification of Malassezia species. Indian J. Med. Microbiol. 22:179–181 [PubMed]
181. Kligman AM. 1979. Perspectives and problems in cutaneous gerontology. J. Invest. Dermatol. 73:39–46 [PubMed]
182. Knockaert M, et al. 2004. Independent actions on cyclin-dependent kinases and aryl hydrocarbon receptor mediate the antiproliferative effects of indirubins. Oncogene 23:4400–4412 [PubMed]
183. Krämer HJ, et al. 2005. Pityriarubins, novel highly selective inhibitors of respiratory burst from cultures of the yeast Malassezia furfur: comparison with the bisindolylmaleimide arcyriarubin A. Chembiochem 6:2290–2297 [PubMed]
184. Krämer HJ, et al. 2005. Malassezin, a novel agonist of the aryl hydrocarbon receptor from the yeast Malassezia furfur, induces apoptosis in primary human melanocytes. Chembiochem 6:860–865 [PubMed]
185. Krisanty RI, Bramono K, Made Wisnu I. 2009. Identification of Malassezia species from pityriasis versicolor in Indonesia and its relationship with clinical characteristics. Mycoses 52:257–262 [PubMed]
186. Kroumpouzos G. 2005. Pityrosporum folliculitis during pregnancy is not pruritic folliculitis of pregnancy. J. Am. Acad. Dermatol. 53:1098–1099 [PubMed]
187. Kumar CP, Kumar SS, Menon T. 2006. Phospholipase and proteinase activities of clinical isolates of Candida from immunocompromised patients. Mycopathologia 161:213–218 [PubMed]
188. Kwon C-S, Grose RK, Riby J, Chen Y-H, Bjeldanes LF. 1994. In vivo production and enzyme-inducing activity of indolo[3,2-b]carbazole. J. Agric. Food Chem. 42:2536–2540
189. Kyriakis KP, Palamaras STI, Pagana G, Michailides C, Emmanuelides S. 2006. Pityriasis versicolor prevalence by age and gender. Mycoses 49:517–518 [PubMed]
190. Larangeira de Almeida H, Jr, Mayser P. 2006. Absence of sunburn in lesions of pityriasis versicolor alba. Mycoses 49:516. [PubMed]
191. Larocco M, Dorenbaum A, Robinson A, Pickering LK. 1988. Recovery of Malassezia pachydermatis from eight infants in a neonatal intensive care nursery: clinical and laboratory features. Pediatr. Infect. Dis. J. 7:398–401 [PubMed]
192. Lautenbach E, Nachamkin I, Schuster MG. 1998. Malassezia pachydermatis infections. N. Engl. J. Med. 339:270–271 [PubMed]
193. Lee WJ, et al. 2011. Disruption of barrier function in dermatophytosis and pityriasis versicolor. J. Dermatol. 38:1049–1053 [PubMed]
194. Lee YW, et al. 2008. Isolation of 19 strains of Malassezia dermatis from healthy human skin in Korea. J. Dermatol. 35:772–777 [PubMed]
195. Lee YW, Yim SM, Lim SH, Choe YB, Ahn KJ. 2006. Quantitative investigation on the distribution of Malassezia species on healthy human skin in Korea. Mycoses 49:405–410 [PubMed]
196. Leeming JP, Holland KT, Bojar RA. 1986. The in vitro antimicrobial effect of azelaic acid. Br. J. Dermatol. 115:551–556 [PubMed]
197. Leeming JP, Notman FH. 1987. Improved methods for isolation and enumeration of Malassezia furfur from human skin. J. Clin. Microbiol. 25:2017–2019 [PMC free article] [PubMed]
198. Levy MS, Polsky D, Davidson A, Strober BE. 2008. Tinea versicolor associated with etanercept therapy. J. Am. Acad. Dermatol. 58:S99–S100 [PubMed]
199. Limacher A, et al. 2007. Cross-reactivity and 1.4-A crystal structure of Malassezia sympodialis thioredoxin (Mala s 13), a member of a new pan-allergen family. J. Immunol. 178:389–396 [PubMed]
200. Lin YK, et al. 2008. Clinical assessment of patients with recalcitrant psoriasis in a randomized, observer-blind, vehicle-controlled trial using indigo naturalis. Arch. Dermatol. 144:1457–1464 [PubMed]
201. Liu H, Wormke M, Safe SH, Bjeldanes LF. 1994. Indolo[3,2-b]carbazole: a dietary-derived factor that exhibits both antiestrogenic and estrogenic activity. J. Natl. Cancer Inst. 86:1758–1765 [PubMed]
202. Lober CW, Belew PW, Rosenberg EW, Bale G. 1982. Patch tests with killed sonicated microflora in patients with psoriasis. Arch. Dermatol. 118:322–325 [PubMed]
203. Long JG, Keyserling HL. 1985. Catheter-related infection in infants due to an unusual lipophilic yeast—Malassezia furfur. Pediatrics 76:896–900 [PubMed]
204. Luecke S, et al. 2010. The aryl hydrocarbon receptor (AHR), a novel regulator of human melanogenesis. Pigment Cell Melanoma Res. 23:828–833 [PubMed]
205. Machado ML, et al. 2010. Genetic variability and phospholipase production of Malassezia pachydermatis isolated from dogs with diverse grades of skin lesions. Med. Mycol. 48:889–892 [PubMed]
206. Machowinski A, Krämer HJ, Hort W, Mayser P. 2006. Pityriacitrin—a potent UV filter produced by Malassezia furfur and its effect on human skin microflora. Mycoses 49:388–392 [PubMed]
207. Makimura K, et al. 2000. Species identification and strain typing of Malassezia species stock strains and clinical isolates based on the DNA sequences of nuclear ribosomal internal transcribed spacer 1 regions. J. Med. Microbiol. 49:29–35 [PubMed]
208. Malassez L. 1874. Note sur le champignon du pityriasis simple. Arch. Physiol. 1:451–459
209. Marcon MJ, Durrell DE, Powell DA, Buesching WJ. 1987. In vitro activity of systemic antifungal agents against Malassezia furfur. Antimicrob. Agents Chemother. 31:951–953 [PMC free article] [PubMed]
210. Marcus LC, Marcus E. 1998. Nosocomial zoonoses. N. Engl. J. Med. 338:757–759 [PubMed]
211. Massone G, Cavalchini A, Clapasson A, Nunzi E. 2010. Hypopigmented macules: leprosy, atopy or pityriasis versicolor. G. Ital. Dermatol. Venereol. 145:779–782 [PubMed]
212. Masure O, et al. 1991. Malassezia furfur septicaemia in a child with leukaemia. J. Infect. 23:335–336 [PubMed]
213. Mayser P, Gaitanis G. 2010. Physiology and biochemistry, p 121–138 In Boekhout T, Guého E, Mayser P, Velegraki A, editors. (ed), Malassezia and the skin. Science and clinical practice. Springer, Berlin, Germany
214. Mayser P, Rieche I. 2009. Rapid reversal of hyperpigmentation in pityriasis versicolor upon short-term topical cycloserine application. Mycoses 52:541–543 [PubMed]
215. Mayser P, Schafer U, Krämer HJ, Irlinger B, Steglich W. 2002. Pityriacitrin—an ultraviolet-absorbing indole alkaloid from the yeast Malassezia furfur. Arch. Dermatol. Res. 294:131–134 [PubMed]
216. Mayser P, et al. 2003. Pityrialactone—a new fluorochrome from the tryptophan metabolism of Malassezia furfur. Antonie Van Leeuwenhoek 84:185–191 [PubMed]
217. McGinley KJ, Leyden JJ, Marples RR, Kligman AM. 1975. Quantitative microbiology of the scalp in non-dandruff, dandruff and seborrheic dermatitis. J. Invest. Dermatol. 64:401–405 [PubMed]
218. Merisalu A, et al. 2007. The contribution of genetic variations of aryl hydrocarbon receptor pathway genes to male factor infertility. Fertil. Steril. 88:854–859 [PubMed]
219. Mickelsen PA, Viano-Paulson MC, Stevens DA, Diaz PS. 1988. Clinical and microbiological features of infection with Malassezia pachydermatis in high-risk infants. J. Infect. Dis. 157:1163–1168 [PubMed]
220. Middleton C, Lowenthal RM. 1987. Malassezia furfur fungemia as a treatable cause of obscure fever in a leukemia patient receiving parenteral nutrition. Aust. N. Z. J. Med. 17:603–604 [PubMed]
221. Midgley G. 1989. The diversity of Pityrosporum (Malassezia) yeasts in vivo and in vitro. Mycopathologia 106:143–153 [PubMed]
222. Midreuil F, et al. 1999. Genetic diversity in the yeast species Malassezia pachydermatis analysed by multilocus enzyme electrophoresis. Int. J. Syst. Bacteriol. 49:1287–1294 [PubMed]
223. Mirhendi H, et al. 2005. A simple PCR-RFLP method for identification and differentiation of 11 Malassezia species. J. Microbiol. Methods 61:281–284 [PubMed]
224. Morishita N, Sei Y, Sugita T. 2006. Molecular analysis of Malassezia microflora from patients with pityriasis versicolor. Mycopathologia 161:61–65 [PubMed]
225. Morris DO. 2005. Malassezia pachydermatis carriage in dog owners. Emerg. Infect. Dis. 11:83–88 [PMC free article] [PubMed]
226. Morrison VA, Weisdorf DJ. 2000. The spectrum of Malassezia infections in the bone marrow transplant population. Bone Marrow Transplant. 26:645–648 [PubMed]
227. Munoz-Perez MA, Rodriguez-Pichardo A, Camacho F, Colmenero MA. 1998. Dermatological findings correlated with CD4 lymphocyte counts in a prospective 3 year study of 1161 patients with human immunodeficiency virus disease predominantly acquired through intravenous drug abuse. Br. J. Dermatol. 139:33–39 [PubMed]
228. Nakabayashi A, Sei Y, Guillot J. 2000. Identification of Malassezia species isolated from patients with seborrhoeic dermatitis, atopic dermatitis, pityriasis versicolor and normal subjects. Med. Mycol. 38:337–341 [PubMed]
229. Naldi L, Rebora A. 2009. Clinical practice. Seborrheic dermatitis. N. Engl. J. Med. 360:387–396 [PubMed]
230. Narang T, Dogra S, Kaur I, Kanwar AJ. 2007. Malassezia and psoriasis: Koebner's phenomenon or direct causation? J. Eur. Acad. Dermatol. Venereol. 21:1111–1112 [PubMed]
231. Nasir A, El Bahesh E, Whitten C, Lawson A, Udall JN., Jr 2010. Pityrosporum folliculitis in a Crohn's disease patient receiving infliximab. Inflamm. Bowel Dis. 16:7–8 [PubMed]
232. Nazzaro-Porro M, Passi S. 1978. Identification of tyrosinase inhibitors in cultures of Pityrosporum. J. Invest. Dermatol. 71:205–208 [PubMed]
233. Nazzaro-Porro M, Passi S, Caprilli F, Mercantini R. 1977. Induction of hyphae in cultures of Pityrosporum by cholesterol and cholesterol esters. J. Invest. Dermatol. 69:355–360 [PubMed]
234. Nestle FO, Di Meglio P, Qin JZ, Nickoloff BJ. 2009. Skin immune sentinels in health and disease. Nat. Rev. Immunol. 9:679–691 [PMC free article] [PubMed]
235. Nguyen ST, Lund CH, Durand DJ. 2001. Thrombolytic therapy for adhesion of percutaneous central venous catheters to vein intima associated with Malassezia furfur infection. J. Perinatol. 21:331–333 [PubMed]
236. Oberle AD, Fowler M, Grafton WD. 1981. Pityrosporum isolate from the upper respiratory tract. Am. J. Clin. Pathol. 76:112–116 [PubMed]
237. Oh BH, Lee YW, Choe YB, Ahn KJ. 2010. Epidemiologic study of Malassezia yeasts in seborrheic dermatitis patients by the analysis of 26S rDNA PCR-RFLP. Ann. Dermatol. 22:149–155 [PMC free article] [PubMed]
238. Oh BH, Song YC, Lee YW, Choe YB, Ahn KJ. 2009. Comparison of nested PCR and RFLP for identification and classification of Malassezia yeasts from healthy human skin. Ann. Dermatol. 21:352–357 [PMC free article] [PubMed]
239. Onishi Y, et al. 1999. Two-dimensional electrophoresis of Malassezia allergens for atopic dermatitis and isolation of Mal f 4 homologs with mitochondrial malate dehydrogenase. Eur. J. Biochem. 261:148–154 [PubMed]
240. Panja G. 1927. The Malassezia of the skin, their cultivation, morphology and species. Abstr. Trans. 7th Congr. Far Eastern Assoc. Trop. Med. 2:442–455
241. Panteleyev AA, Bickers DR. 2006. Dioxin-induced chloracne—reconstructing the cellular and molecular mechanisms of a classic environmental disease. Exp. Dermatol. 15:705–730 [PubMed]
242. Papavassilis C, Mach KK, Mayser PA. 1999. Medium-chain triglycerides inhibit growth of Malassezia: implications for prevention of systemic infection. Crit. Care Med. 27:1781–1786 [PubMed]
243. Paulino LC, Tseng CH, Blaser MJ. 2008. Analysis of Malassezia microbiota in healthy superficial human skin and in psoriatic lesions by multiplex real-time PCR. FEMS Yeast Res. 8:460–471 [PubMed]
244. Paulino LC, Tseng CH, Strober BE, Blaser MJ. 2006. Molecular analysis of fungal microbiota in samples from healthy human skin and psoriatic lesions. J. Clin. Microbiol. 44:2933–2941 [PMC free article] [PubMed]
245. Pechere M, et al. 1999. Malassezia spp carriage in patients with seborrheic dermatitis. J. Dermatol. 26:558–561 [PubMed]
246. Pierard J, Dockx P. 1972. The ultrastructure of tinea versicolor and Malassezia furfur. Int. J. Dermatol. 11:116–124 [PubMed]
247. Pitkaranta M, et al. 2008. Analysis of fungal flora in indoor dust by ribosomal DNA sequence analysis, quantitative PCR, and culture. Appl. Environ. Microbiol. 74:233–244 [PMC free article] [PubMed]
248. Pohjanvirta R, et al. 2002. Comparison of acute toxicities of indolo[3,2-b]carbazole (ICZ) and 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in TCDD-sensitive rats. Food Chem. Toxicol. 40:1023–1032 [PubMed]
249. Pope M, et al. 1994. Conjugates of dendritic cells and memory T lymphocytes from skin facilitate productive infection with HIV-1. Cell 78:389–398 [PubMed]
250. Potter BS, Burgoon CF, Jr, Johnson WC. 1973. Pityrosporum folliculitis. Report of seven cases and review of the Pityrosporum organism relative to cutaneous disease. Arch. Dermatol. 107:388–391 [PubMed]
251. Powell DA, Aungst J, Snedden S, Hansen N, Brady M. 1984. Broviac catheter-related Malassezia furfur sepsis in five infants receiving intravenous fat emulsions. J. Pediatr. 105:987–990 [PubMed]
252. Prober CG, Ein SH. 1984. Tinea versicolor, or how far can furfur go? Pediatr. Infect. Dis. J. 3:592 [PubMed]
253. Prochazkova J, Kozubik A, Machala M, Vondracek J. 2011. Differential effects of indirubin and 2,3,7,8-tetrachlorodibenzo-p-dioxin on the aryl hydrocarbon receptor (AhR) signalling in liver progenitor cells. Toxicology 279:146–154 [PubMed]
254. Prohic A. 2010. Distribution of Malassezia species in seborrhoeic dermatitis: correlation with patients' cellular immune status. Mycoses 53:344–349 [PubMed]
255. Prohic A, Ozegovic L. 2007. Malassezia species isolated from lesional and non-lesional skin in patients with pityriasis versicolor. Mycoses 50:58–63 [PubMed]
256. Pryce TM, Palladino S, Kay ID, Coombs GW. 2003. Rapid identification of fungi by sequencing the ITS1 and ITS2 regions using an automated capillary electrophoresis system. Med. Mycol. 41:369–381 [PubMed]
257. Pryce TM, et al. 2006. Rapid identification of fungal pathogens in BacT/ALERT, BACTEC, and BBL MGIT media using polymerase chain reaction and DNA sequencing of the internal transcribed spacer regions. Diagn. Microbiol. Infect. Dis. 54:289–297 [PubMed]
258. Puig L, Fernandez-Figueras MT, Ferrandiz C, Ribera M, de Moragas JM. 1995. Epidermal expression of 65 and 72 kd heat shock proteins in psoriasis and AIDS-associated psoriasiform dermatitis. J. Am. Acad. Dermatol. 33:985–989 [PubMed]
259. Rasi A, et al. 2010. Malassezia yeast species isolated from Iranian patients with pityriasis versicolor in a prospective study. Mycoses 53:350–355 [PubMed]
260. Ray S, Swanson HI. 2009. Activation of the aryl hydrocarbon receptor by TCDD inhibits senescence: a tumor promoting event? Biochem. Pharmacol. 77:681–688 [PMC free article] [PubMed]
261. Redline RW, Dahms BB. 1981. Malassezia pulmonary vasculitis in an infant on long-term intralipid therapy. N. Engl. J. Med. 305:1395–1398 [PubMed]
262. Redline RW, Redline SS, Boxerbaum B, Dahms BB. 1985. Systemic Malassezia furfur infections in patients receiving intralipid therapy. Hum. Pathol. 16:815–822 [PubMed]
263. Rhie S, Turcios R, Buckley H, Suh B. 2000. Clinical features and treatment of Malassezia folliculitis with fluconazole in orthotopic heart transplant recipients. J. Heart Lung Transplant. 19:215–219 [PubMed]
264. Ribbing C, et al. 2011. Mast cells generated from patients with atopic eczema have enhanced levels of granule mediators and an impaired dectin-1 expression. Allergy 66:110–119 [PubMed]
265. Richet HM, McNeil MM, Edwards MC, Jarvis WR. 1989. Cluster of Malassezia furfur pulmonary infections in infants in a neonatal intensive-care unit. J. Clin. Microbiol. 27:1197–1200 [PMC free article] [PubMed]
266. Rivolta S. 1873. Parasiti vegetali, 1st ed Giulio Speirani, Torino, Italy
267. Robin C. 1853. Histoire naturelle des végétaux parasites qui croissent sur l'homme et les animaux vivants. Baillière, Paris, France
268. Roe E, et al. 2006. Description and management of cutaneous side effects during cetuximab or erlotinib treatments: a prospective study of 30 patients. J. Am. Acad. Dermatol. 55:429–437 [PubMed]
269. Romano C, Maritati E, Ghilardi A, Miracco C, Mancianti F. 2005. A case of pityriasis versicolor atrophicans. Mycoses 48:439–441 [PubMed]
270. Rosales CM, Jackson MA, Zwick D. 2004. Malassezia furfur meningitis associated with total parenteral nutrition subdural effusion. Pediatr. Dev. Pathol. 7:86–90 [PubMed]
271. Rosenberg EW, Belew PW. 1982. Improvement of psoriasis of the scalp with ketoconazole. Arch. Dermatol. 118:370–371 [PubMed]
272. Rothwell TL, Howlett CR, Middleton DJ, Griffiths DA, Duff BC. 1987. Skin neoplasms of dogs in Sydney. Aust. Vet. J. 64:161–164 [PubMed]
273. Saaf AM, et al. 2008. Global expression profiling in atopic eczema reveals reciprocal expression of inflammatory and lipid genes. PLoS One 3:e4017. [PMC free article] [PubMed]
274. Sabouraud R. 1904. Maladies du cuir chevelu. II. Les maladies desquamatives. Masson & Cie, Paris, France
275. Salah SB, et al. 2005. Identification of Malassezia species from Tunisian patients with pityriasis versicolor and normal subjects. Mycoses 48:242–245 [PubMed]
276. Sanchez JL, Torres VM. 1984. Double-blind efficacy study of selenium sulfide in tinea versicolor. J. Am. Acad. Dermatol. 11:235–238 [PubMed]
277. Sandström Falk MH, et al. 2005. The prevalence of Malassezia yeasts in patients with atopic dermatitis, seborrhoeic dermatitis and healthy controls. Acta Derm. Venereol. 85:17–23 [PubMed]
278. Schleman KA, Tullis G, Blum R. 2000. Intracardiac mass complicating Malassezia furfur fungemia. Chest 118:1828–1829 [PubMed]
279. Schmid-Grendelmeier P, et al. 2005. IgE-mediated and T cell-mediated autoimmunity against manganese superoxide dismutase in atopic dermatitis. J. Allergy Clin. Immunol. 115:1068–1075 [PubMed]
280. Schoepfer C, et al. 1995. Malassezia furfur septicemia after bone marrow graft. Arch. Pediatr. 2:245–248 [PubMed]
281. Schrenk D, Riebniger D, Till M, Vetter S, Fiedler HP. 1997. Tryptanthrins: a novel class of agonists of the aryl hydrocarbon receptor. Biochem. Pharmacol. 54:165–171 [PubMed]
282. Selander C, Engblom C, Nilsson G, Scheynius A, Andersson CL. 2009. TLR2/MyD88-dependent and -independent activation of mast cell IgE responses by the skin commensal yeast Malassezia sympodialis. J. Immunol. 182:4208–4216 [PubMed]
283. Shek YH, Tucker MC, Viciana AL, Manz HJ, Connor DH. 1989. Malassezia furfur—disseminated infection in premature infants. Am. J. Clin. Pathol. 92:595–603 [PubMed]
284. Shi VS, Lio PA. 2011. Diagnosis of pityriasis versicolor in paediatrics: the evoked scale sign. Arch. Dis. Child. 96:392–393 [PubMed]
285. Shibata N, et al. 2006. Isolation, characterization and molecular cloning of a lipolytic enzyme secreted from Malassezia pachydermatis. FEMS Microbiol. Lett. 256:137–144 [PubMed]
286. Shokohi T, Afshar P, Barzgar A. 2009. Distribution of Malassezia species in patients with pityriasis versicolor in Northern Iran. Indian J. Med. Microbiol. 27:321–324 [PubMed]
287. Shparago NI, Bruno PP, Bennett J. 1995. Systemic Malassezia furfur infection in an adult receiving total parenteral nutrition. J. Am. Osteopath. Assoc. 95:375–377 [PubMed]
288. Shuster S. 1984. The aetiology of dandruff and the mode of action of therapeutic agents. Br. J. Dermatol. 111:235–242 [PubMed]
289. Silva V, Moreno GA, Zaror L, de-Oliveira E, Fischman O. 1997. Isolation of Malassezia furfur from patients with onychomycosis. J. Med. Vet. Mycol. 35:73–74 [PubMed]
290. Simmons RB, Guého E. 1990. A new species of Malassezia. Mycol. Res. 94:1146–1149
291. Sizun J, et al. 1994. Malassezia furfur-related colonization and infection of central venous catheters. A prospective study in a pediatric intensive care unit. Intensive Care Med. 20:496–499 [PubMed]
292. Slooff WC. 1970. Genus 6 Pityrosporum Sabouraud, p 1167–1186 In Lodder J, editor. (ed), The yeasts, a taxonomic study, 2nd ed. North-Holland, Amsterdam, Netherlands:
293. Sternberg TH, Keddie MD. 1961. Immunofluorescence studies in tinea versicolor. Arch. Dermatol. 84:999–1003 [PubMed]
294. Sugita T, et al. 2003. Sequence diversity of the intergenic spacer region of the rRNA gene of Malassezia globosa colonizing the skin of patients with atopic dermatitis and healthy individuals. J. Clin. Microbiol. 41:3022–3027 [PMC free article] [PubMed]
295. Sugita T, et al. 2001. Molecular analysis of Malassezia microflora on the skin of atopic dermatitis patients and healthy subjects. J. Clin. Microbiol. 39:3486–3490 [PMC free article] [PubMed]
296. Sugita T, Tajima M, Amaya M, Tsuboi R, Nishikawa A. 2004. Genotype analysis of Malassezia restricta as the major cutaneous flora in patients with atopic dermatitis and healthy subjects. Microbiol. Immunol. 48:755–759 [PubMed]
297. Sugita T, et al. 2004. A new yeast, Malassezia yamatoensis, isolated from a patient with seborrheic dermatitis, and its distribution in patients and healthy subjects. Microbiol. Immunol. 48:579–583 [PubMed]
298. Sugita T, Tajima M, Tsubuku H, Tsuboi R, Nishikawa A. 2006. Quantitative analysis of cutaneous Malassezia in atopic dermatitis patients using real-time PCR. Microbiol. Immunol. 50:549–552 [PubMed]
299. Sugita T, Takashima M, Kodama M, Tsuboi R, Nishikawa A. 2003. Description of a new yeast species, Malassezia japonica, and its detection in patients with atopic dermatitis and healthy subjects. J. Clin. Microbiol. 41:4695–4699 [PMC free article] [PubMed]
300. Sugita T, et al. 2002. New yeast species, Malassezia dermatis, isolated from patients with atopic dermatitis. J. Clin. Microbiol. 40:1363–1367 [PMC free article] [PubMed]
301. Sutter CH, et al. 2009. EGF receptor signaling blocks aryl hydrocarbon receptor-mediated transcription and cell differentiation in human epidermal keratinocytes. Proc. Natl. Acad. Sci. U. S. A. 106:4266–4271 [PubMed]
302. Suwattee P, Cham PM, Solomon RK, Kaye VN. 2009. Tinea versicolor with interface dermatitis. J. Cutan. Pathol. 36:285–286 [PubMed]
303. Suzuki T, Hori N, Miyake T, Hori Y, Mochizuki K. 2007. Keratitis caused by a rare fungus, Malassezia restricta. Jpn. J. Ophthalmol. 51:292–294 [PubMed]
304. Suzuki T, Ohno N, Ohshima Y, Yadomae T. 2000. Modulation of calcium-induced clot formation of human plasma by Malassezia furfur. Zentralbl. Bakteriol. 289:849–856 [PubMed]
305. Suzuki T, Ohno N, Ohshima Y, Yadomae T. 1998. Soluble mannan and beta-glucan inhibit the uptake of Malassezia furfur by human monocytic cell line, THP-1. FEMS Immunol. Med. Microbiol. 21:223–230 [PubMed]
306. Suzuki T, Tsuzuki A, Ohno N, Ohshima Y, Yadomae T. 2000. Enhancement of IL-8 production from human monocytic and granulocytic cell lines, THP-1 and HL-60, stimulated with Malassezia furfur. FEMS Immunol. Med. Microbiol. 28:157–162 [PubMed]
307. Tajima M, Sugita T, Nishikawa A, Tsuboi R. 2008. Molecular analysis of Malassezia microflora in seborrheic dermatitis patients: comparison with other diseases and healthy subjects. J. Invest. Dermatol. 128:345–351 [PubMed]
308. Takahata Y, Sugita T, Hiruma M, Muto M. 2007. Quantitative analysis of Malassezia in the scale of patients with psoriasis using a real-time polymerase chain reaction assay. Br. J. Dermatol. 157:670–673 [PubMed]
309. Takei Y, et al. 2003. Tryptanthrin inhibits interferon-gamma production by Peyer's patch lymphocytes derived from mice that had been orally administered staphylococcal enterotoxin. Biol. Pharm. Bull. 26:365–367 [PubMed]
310. Tanaka M, Imamura S. 1979. Immunological studies on Pityrosporum genus and Malassezia furfur. J. Invest. Dermatol. 73:321–324 [PubMed]
311. Tarazooie B, et al. 2004. Study of the distribution of Malassezia species in patients with pityriasis versicolor and healthy individuals in Tehran, Iran. BMC Dermatol. 4:5. [PMC free article] [PubMed]
312. Tateno H, et al. 2010. Dual specificity of Langerin to sulfated and mannosylated glycans via a single C-type carbohydrate recognition domain. J. Biol. Chem. 285:6390–6400 [PMC free article] [PubMed]
313. Taylor GD, Buchanan-Chell M, Kirkland T, McKenzie M, Wiens R. 1994. Trends and sources of nosocomial fungaemia. Mycoses 37:187–190 [PubMed]
314. Terragni L, Lasagni A, Oriani A, Gelmetti C. 1991. Pityriasis versicolor in the pediatric age. Pediatr. Dermatol. 8:9–12 [PubMed]
315. Theelen B, Silvestri M, Guého E, van Belkum A, Boekhout T. 2001. Identification and typing of Malassezia yeasts using amplified fragment length polymorphism (AFLP), random amplified polymorphic DNA (RAPD) and denaturing gradient gel electrophoresis (DGGE). FEMS Yeast Res. 1:79–86 [PubMed]
316. Thomas DS, Ingham E, Bojar RA, Holland KT. 2008. In vitro modulation of human keratinocyte pro- and anti-inflammatory cytokine production by the capsule of Malassezia species. FEMS Immunol. Med. Microbiol. 54:203–214 [PubMed]
317. Tschachler E, Bergstresser PR, Stingl G. 1996. HIV-related skin diseases. Lancet 348:659–663 [PubMed]
318. Unna PG. 1887. Seborrheic eczema. J. Cutan. Dis. 5:449–453
319. van Belkum A, Boekhout T, Bosboom R. 1994. Monitoring spread of Malassezia infections in a neonatal intensive care unit by PCR-mediated genetic typing. J. Clin. Microbiol. 32:2528–2532 [PMC free article] [PubMed]
320. Velegraki A, Alexopoulos EC, Kritikou S, Gaitanis G. 2004. Use of fatty acid RPMI 1640 media for testing susceptibilities of eight Malassezia species to the new triazole posaconazole and to six established antifungal agents by a modified NCCLS M27-A2 microdilution method and Etest. J. Clin. Microbiol. 42:3589–3593 [PMC free article] [PubMed]
321. Vilhelmsson M, et al. 2008. Mutational analysis of amino acid residues involved in IgE-binding to the Malassezia sympodialis allergen Mala s 11. Mol. Immunol. 46:294–303 [PubMed]
322. Vilhelmsson M, et al. 2007. Crystal structure of the major Malassezia sympodialis allergen Mala s 1 reveals a beta-propeller fold: a novel fold among allergens. J. Mol. Biol. 369:1079–1086 [PubMed]
323. Vlachos C, et al. 2009. Phospholipase production by Malassezia species in response to beta-endorphin stimulation: a candidate virulence factor? Mycoses 52:105
324. Vlachos C, et al. 2011. Malassezia produced indoles induce aryl hydrocarbon receptor activation and inhibit Toll-like receptor maturation in monocyte derived dendritic cells. J. Invest. Dermatol. 131:S87 [PubMed]
325. von Bomhard W, et al. 2007. Cutaneous neoplasms in pet rabbits: a retrospective study. Vet. Pathol. 44:579–588 [PubMed]
326. Wahab MA, et al. 2010. Single dose (400 mg) versus 7 day (200 mg) daily dose itraconazole in the treatment of tinea versicolor: a randomized clinical trial. Mymensingh Med. J. 19:72–76 [PubMed]
327. Wallace M, Bagnall H, Glen D, Averill S. 1979. Isolation of lipophilic yeast in “sterile” peritonitis. Lancet ii:956. [PubMed]
328. Wanke I, et al. 2011. Skin commensals amplify the innate immune response to pathogens by activation of distinct signaling pathways. J. Invest. Dermatol. 131:382–390 [PubMed]
329. Watanabe S, Kano R, Sato H, Nakamura Y, Hasegawa A. 2001. The effects of Malassezia yeasts on cytokine production by human keratinocytes. J. Invest. Dermatol. 116:769–773 [PubMed]
330. Wei YD, Helleberg H, Rannug U, Rannug A. 1998. Rapid and transient induction of CYP1A1 gene expression in human cells by the tryptophan photoproduct 6-formylindolo[3,2-b]carbazole. Chem. Biol. Interact. 110:39–55 [PubMed]
331. Weichel M, Flückiger S, Crameri R. 2002. Molecular characterization of mould allergens involved in respiratory complications. Recent Res. Dev. Respir. Crit. Care Med. 2:29–45
332. Weidman FD. 1925. Exfoliative dermatitis in the Indian rhinoceros (Rhinoceros unicornis), with description of a new species: Pityrosporum pachydermatis, p 36–43 In Fox H, editor. (ed), Report of the Laboratory and Museum of Comparative Pathology of the Zoological Society of Philadelphia. Laboratory and Museum of Comparative Pathology of the Zoological Society of Philadelphia, Philadelphia, PA
333. Weiss SJ, Schoch PE, Cunha BA. 1991. Malassezia furfur fungemia associated with central venous catheter lipid emulsion infusion. Heart Lung 20:87–90 [PubMed]
334. Werfel T. 2009. The role of leukocytes, keratinocytes, and allergen-specific IgE in the development of atopic dermatitis. J. Invest. Dermatol. 129:1878–1891 [PubMed]
335. Wikler JR, Nieboer C, Willemze R. 1992. Quantitative skin cultures of Pityrosporum yeasts in patients seropositive for the human immunodeficiency virus with and without seborrheic dermatitis. J. Am. Acad. Dermatol. 27:37–39 [PubMed]
336. Wille G, et al. 2001. Malassezin—a novel agonist of the arylhydrocarbon receptor from the yeast Malassezia furfur. Bioorg. Med. Chem. 9:955–960 [PubMed]
337. Wurtz RM, Knospe WN. 1988. Malassezia furfur fungemia in a patient without the usual risk factors. Ann. Intern. Med. 109:432–433 [PubMed]
338. Xu J, et al. 2007. Dandruff-associated Malassezia genomes reveal convergent and divergent virulence traits shared with plant and human fungal pathogens. Proc. Natl. Acad. Sci. U. S. A. 104:18730–18735 [PubMed]
339. Xue C, Hsueh YP, Heitman J. 2008. Magnificent seven: roles of G protein-coupled receptors in extracellular sensing in fungi. FEMS Microbiol. Rev. 32:1010–1032 [PMC free article] [PubMed]
340. Yamasaki S, et al. 2009. C-type lectin Mincle is an activating receptor for pathogenic fungus, Malassezia. Proc. Natl. Acad. Sci. U. S. A. 106:1897–1902 [PubMed]
341. Yang YS, Shin MK, Haw CR. 2010. Atrophying pityriasis versicolor: is this a new variant of pityriasis versicolor? Ann. Dermatol. 22:456–459 [PMC free article] [PubMed]
342. Yarrow D, Ahearn D. 1984. Genus 7 Malassezia Baillon, p 882–885 In Kreger-van Rij NJW, editor. (ed), The yeasts, a taxonomic study, 3rd ed. Elsevier Science, Amsterdam, Netherlands
343. Yates VM, Kerr RE, Frier K, Cobb SJ, MacKie RM. 1983. Early diagnosis of infantile seborrhoeic dermatitis and atopic dermatitis—total and specific IgE levels. Br. J. Dermatol. 108:639–645 [PubMed]
344. Yim SM, et al. 2010. Molecular analysis of Malassezia microflora on the skin of the patients with atopic dermatitis. Ann. Dermatol. 22:41–47 [PMC free article] [PubMed]
345. Youn SW, Na JI, Choi SY, Huh CH, Park KC. 2005. Regional and seasonal variations in facial sebum secretions: a proposal for the definition of combination skin type. Skin Res. Technol. 11:189–195 [PubMed]
346. Yu ST, Chen TM, Tseng SY, Chen YH. 2007. Tryptanthrin inhibits MDR1 and reverses doxorubicin resistance in breast cancer cells. Biochem. Biophys. Res. Commun. 358:79–84 [PubMed]
347. Zargari A, Midgley G, Bäck O, Johansson SG, Scheynius A. 2003. IgE-reactivity to seven Malassezia species. Allergy 58:306–311 [PubMed]
348. Zargari A, et al. 2007. Mala s 12 is a major allergen in patients with atopic eczema and has sequence similarities to the GMC oxidoreductase family. Allergy 62:695–703 [PubMed]
349. Zawar V, Chuh A. 2009. Case report on Malassezia infection of palms and fingernails—speculations on cause for therapeutic failure in pityriasis versicolor. J. Eur. Acad. Dermatol. Venereol. 23:171–172 [PubMed]
350. Zhang H, et al. 2010. Genetic polymorphism of Malassezia furfur isolates from Han and Tibetan ethnic groups in China using DNA fingerprinting. Med. Mycol. 48:1034–1038 [PubMed]
351. Zhao Y, Li L, Wang JJ, Kang KF, Zhang QQ. 2010. Cutaneous malasseziasis: four case reports of atypical dermatitis and onychomycosis caused by Malassezia. Int. J. Dermatol. 49:141–145 [PubMed]
352. Zitvogel L, Tesniere A, Kroemer G. 2006. Cancer despite immunosurveillance: immunoselection and immunosubversion. Nat. Rev. Immunol. 6:715–727 [PubMed]
353. Zomorodian K, et al. 2008. Distribution of Malassezia species in patients with psoriasis and healthy individuals in Tehran, Iran. J. Cutan. Pathol. 35:1027–1031 [PubMed]
354. Zouboulis CC, et al. 2008. Frontiers in sebaceous gland biology and pathology. Exp. Dermatol. 17:542–551 [PubMed]
355. Zuther K, et al. 2008. The tryptophan aminotransferase Tam1 catalyses the single biosynthetic step for tryptophan-dependent pigment synthesis in Ustilago maydis. Mol. Microbiol. 68:152–172 [PubMed]

Articles from Clinical Microbiology Reviews are provided here courtesy of American Society for Microbiology (ASM)