Recent advances in medical therapies, organ transplantation, HIV infections, and an increasing geriatric population have generated rising populations of immunocompromised patients. These events have all resulted in a significant increase in life-threatening human fungal infections over the last two decades (1
). The limited treatment options and high mortality rates associated with these infections has consequently led to a concerted effort to better understand mechanisms of fungal pathogenesis in mammals. The general rationale behind these studies is that a better understanding of how these organisms cause disease will allow us to develop better technologies for the treatment and prevention of these often lethal infections. One increasing area of fungal pathogenesis research is related to identifying and understanding the basic metabolic pathways utilized by these fungi to survive in the harsh and highly variable mammalian host environment.
The three main fungal pathogens that cause human mycoses, Aspergillus fumigatus, Cryptococcus neoformans, and Candida albicans, are typically opportunistic pathogens. These fungi are saprophytic organisms that have evolved a unique combination of attributes to survive in their natural environments. Aspergillus fumigatus is typically found in soil and decaying organic material such as compost heaps. Cryptococcus neoformans is typically found in pigeon droppings, soil and certain trees. Unlike Aspergillus and Cryptococcus species, Candida albicans is rarely found in the soil or external environment. Instead, it is a normal inhabitant of the human microflora. Thus, C. albicans is already highly adapted to the host environment. C. albicans possess the ability to survive in disparate host environments, as illustrated by its ability to colonize diverse areas of the host (oral, vaginal, gastrointestinal areas). Coincidentally, many of these attributes, which allow fungal survival in their natural ecological niches, appear to also allow these fungi to cause disease in immunocompromised hosts. One overlooked environmental selection pressure found in natural environments of all three of the most common fungal pathogens of humans is low oxygen tension. Whether in the soil, a compost pile, pigeon guano, or the gut of a mammal, these fungi must deal with low levels of oxygen.
The focus of this review is on the increasing evidence that pathogenic fungi must adapt to rapidly changing oxygen levels during fungal infections. It is well established that oxygen levels vary throughout the mammalian body depending on numerous factors including tissue type and presence or absence of an inflammatory response. For example, oxygen levels in most mammalian tissues are found to be considerably below atmospheric levels (21%) (2
). Even in the alveoli of healthy lungs, the most oxygen rich organ and site of infection for many fungal pathogens, the oxygen level is around 14%. By the time oxygen reaches the capillaries and diffuses into surrounding tissues its availability is much lower with levels of 2-4% reported (5
). In addition, it is well established that at sites of inflammation available oxygen is significantly reduced compared to surrounding tissues (7
). Moreover, in inflamed tissues, the blood supply is often interrupted because the vessels are congested with phagocytes or the pathogen itself (10
). Thus, it seems highly probable that hypoxic microenvironments are generated during fungal infection.
Indeed, we can look no further than the host response to observe that fungal pathogens are likely exposed to severely low oxygen levels during infection. Immune effector cells, such as neutrophils, function effectively in severely hypoxic microenvironments. These and other cells of the host have evolved distinct mechanisms to deal with hypoxic microenvironments generated during microbial infections. Many of these host response mechanisms are dependent upon the global transcription factor, hypoxia inducible factor (HIF) 1.
HIF 1 is a heterodimeric transcription factor that consists of one of three α-subunits (HIF-1α, HIF-2α, and HIF-3α) and one β-subunit (HIF-1β), and is the central regulator of hypoxic gene expression in mammals (reviewed in (12
)). Both the degradation and activity of the HIF-1α subunit are regulated by oxygen-dependent post-translational hydroxyl modifications. Under hypoxic conditions HIF-1α is not hydroxylated, leading to an accumulation of the HIF-1α subunit and expression of hypoxia-responsive genes, including those encoding many glycolytic enzymes, erythropoietin, adrenomedullin, and growth factors (14
In a recent study of A
yndrome (ARDS) and acute inflammatory lung injury, Thiel et al.
) provided evidence for the importance of hypoxic microenvironments in regulation of host immune responses. ARDS patients are normally treated with a life-saving oxygen therapy, but this therapy may have a dangerous side effect in patients with uncontrolled pulmonary inflammation. Thiel et al.
) identified a local tissue hypoxia-driven and adenosin A2A receptor (A2AR)-mediated anti-inflammatory mechanism. Their data suggest that oxygenation may lead to elimination of the A2AR-mediated lung tissue-protecting pathway and thereby further exacerbate lung injury. Taken together, the above observations and studies indicate that mammalian immune system responses to microbial infection and inflammation are critically tied to hypoxic microenvironments.
While the role of hypoxia in the immune response to fungal pathogens is relatively unknown, it follows that since immune cells of the host have evolved mechanisms to function in hypoxia, mammalian fungal pathogens like A. fumigatus
, C. neoformans
and C. albicans
are likely exposed to hypoxic conditions during fungal pathogenesis. Indeed, during A. fumigatus
infection, our laboratory has recently observed significant increases in HIF-1α activity as the fungal infection progresses and inflammation and edema increase in the lung (Grahl and Cramer, unpublished data). In addition, a recent study by Brock et al.
) demonstrated that hypoxia likely occurs in vivo
in the lung during A fumigatus
infection. The authors constructed a luciferase-producing bioluminescent A. fumigatus
strain, which was not attenuated in virulence in a murine model of invasive aspergillosis. Interestingly, luminescence from the lungs decreased after reaching a maximum at one day post infection, despite the high number of fungal hyphae present in histology examinations. The authors hypothesize that this phenomenon might be due to the severe tissue damage in and through the pulmonary lesions, which likely decrease the oxygen concentration in the lung tissue. Oxygen is essential for the light-producing reaction, and thus the lack of luminescence is likely attributable to the hypoxia at the site of infection (17
Additional evidence that hypoxia may be a key component of the pathophysiology of invasive fungal infections comes from the observation that there are often significant differences in the in vivo
and in vitro
test results of antifungal drug efficacies. These differences have recently been postulated to be related to hypoxic conditions found in vivo
as demonstrated by in vitro
antifungal drug efficacy tests conducted in hypoxia (6
). Furthermore, recent studies have identified genes responsible for regulating fungal response to hypoxia, and some of these pathways have been observed to be essential for fungal virulence of mammals. Consequently, it seems probable that pathogenic fungi possess mechanisms to adapt to hypoxic microenvironments found in vivo
The purpose of this review is to summarize recent advances in our understanding of mechanisms that human fungal pathogens use to adapt to hypoxic conditions and to highlight the emerging importance of this area of research in the pathogenic fungi. While studies on hypoxia adaptation in these pathogenic fungi are limited, increasing research attention to this important component of their virulence arsenal has revealed similarities and differences with each other and the model yeast S. cerevisiae and S. pombe. Importantly, we should clarify the distinction between mechanisms of hypoxia adaptation and mechanisms of hypoxic growth. It seems clear that these are two distinct biological processes requiring a distinct set of genes and mechanisms. In our literature review, we did not find detailed studies defining these two likely different processes in the fungi. It is likely that periods of adaptation are different for diverse fungi. A close examination of the methodology used in the cited studies indicated that most, if not all, studies are focused on genes allowing the fungi to adapt to hypoxia (i.e. genes expressed/required in the early phase of exposure to hypoxia (within 48 hours of a switch to hypoxia), rather than genes required for actual fungal growth in these conditions. Where possible, we have attempted to highlight these distinctions. Finally, we have divided the manuscript into sections detailing fungi with Upc2p orthologs and fungi with SREBP orthologs given the emerging importance of these pathways in oxygen sensing and hypoxia adaptation in fungi.
Fungi with the SREBP analogue Upc2p
Saccharomyces cerevisiae S. cerevisiae
cells adapt to anaerobic conditions by inducing expression of a large number of genes, called “hypoxic genes” (19
). The hypoxic genes encode oxygen-related functions in respiration, heme, and membrane biosynthesis that are required at higher levels when molecular oxygen is limited (20
). For the regulation of hypoxic genes, the cell senses oxygen availability through cellular heme levels (27
), and recent studies suggest that oxygen availability can also be sensed through cellular sterol levels (29
Oxygen sensing by heme
Molecular oxygen is required as a substrate in two consecutive steps of heme biosynthesis catalyzed by the enzymes coproporphyrinogen oxidase and protoporphyrinogen IX oxidase (30
). In the presence of oxygen (aerobic growth), heme accumulates, binds to the transcriptional activator Hap1p (H
rotein) and causes the formation of a Hap1p homodimer specific for DNA binding to the cis-
element. Hap1p is a protein composed of a zinc-finger DNA binding domain at the N-terminus, a dimerization domain, a heme binding domain within the central region, a heme-responsive motif 7 (HRM7), and a transcriptional activation domain at the C-terminus (31
). The heme-Hap1p-complex acts as a transcriptional activator of genes containing its recognition site (5′CGGN6
), such as genes involved in respiration (reviewed in (20
In addition, the expression of the ROX1
ic genes) gene is activated by the heme-Hap1p complex and Rox1p accumulates in the cell under aerobic conditions (reviewed in (26
)). The Rox1p repressor binds to its recognition site upstream of the hypoxic genes to repress their transcription (37
). Rox1p binds to the DNA with its HMG domain and recruits the general repression complex, Tup1/Ssn6, which binds to the Rox1p repression domain (reviewed in (26
)). The repression through Rox1p varies between hypoxic genes that do not have aerobic counterparts, which are expressed at detectable levels at all oxygen concentrations but their expression is higher when oxygen decreases, like HEM13
, and the autorepressed ROX1
itself, and hypoxic genes that have an aerobic homologue, like HMG1/HMG2
, AAC1, AAC2/AAC3
, and TIF51A/ANBI
(the first gene is aerobic – last and underlined anaerobic). The anaerobic gene is then completely repressed until very low oxygen concentrations are reached (38
For some hypoxic genes, a second DNA binding protein Mot3p enhances Rox1p repression through helping recruit the Tup1p/Ssn6p complex. Two examples are the ANBI
nduced) gene, encoding a subunit of eukaryotic initiation factor 5 (eIF-5a), an essential translation factor (40
), and the HEM13
gene, encoding the enzyme coproporphyrinogen III oxidase, which catalyzes the rate-limiting step in heme biosynthesis (41
). The hypoxic derepression of HEM13
allows the cell to continue heme biosynthesis under limited available oxygen. The strongly repressed ANBI
gene has one Mot3p and two Rox1p binding sites in its promoter region, while the promoter of the partially repressed HEM13
contains one Rox1p and three Mot3p binding sites. The combination of binding sites determines the strength of repression. Multiple Mot3p binding sites plus a single Rox1p binding site are much weaker than multiple Rox1p binding sites plus a single Mot3p binding site (42
). Rox1p and Mot3p both interact with Ssn6p of the general repression complex and Rox1p stabilizes Mot3p binding to DNA through interactions with Tup1p/Ssn6p (42
Under hypoxic or anaerobic growth conditions, heme levels are reduced. Hap1p still binds to its cognate site, but in the absence of heme, Hap1p forms a biochemically distinct H
omplex, HMC, which contains Hap1p and four other proteins including Hsp28p and Ydj1p. This complex represses transcription (43
). Consequently, under hypoxic conditions, ROX1
expression is repressed resulting in the activation of hypoxic genes expression. (26
During adaptation to anaerobic conditions, a complex program of cell wall remodeling occurs in yeast. Under anaerobic conditions, major aerobic cell wall mannoproteins, encoded by CWP1
are replaced by their anaerobic counterparts, encoded by the DAN
genes. The DAN
genes encode a group of eight cell wall mannoproteins that play a significant role in cell wall permeability (23
genes are regulated by heme, sterol levels, and three DNA binding transcription factors. The heme-dependent repressors Rox1p and Mot3p function synergistically to efficiently repress DAN
genes under aerobic conditions (45
). In addition, the sterol depletion-dependent activator Upc2p acts through a consensus site termed AR1
to induce the expression of DAN
genes in anaerobic conditions (46
). Sertil et al.
) observed that the histone deacetylase and global repressor Rpd3p is required for the expression of all the DAN
genes and the hypoxic gene ANBI
. Moreover, the authors propose that Rpd3p is recruited to the DAN1
promoter under strict anaerobic conditions. The presence of Rpd3p at the promoter counteracts the function of the repressor Mot3p, which leads to stable binding of the activator Upc2p. Upc2p then recruits the chromatin remodeling complex Swi/Snf to reorganize chromatin, thereby facilitating the binding of the transcriptional machinery that results in the activation of gene expression (47
). Upc2p, together with the transcription factor Ecm22p, is also responsible for basal and induced expression of genes encoding enzymes of ergosterol biosynthesis in yeast (ERG1
, and ERG27
), and it has been implicated in the uptake of sterols under hypoxic conditions (48
Oxygen sensing by sterols
While heme has been thought to be the primary oxygen sensor in S. cerevisiae
, recent studies suggest that sterol levels also play an important role. Upc2p and Ecm22p are functionally related to human sterol regulatory element binding protein (SREBP) with an N-terminal transcription factor domain and a C-terminal transmembrane domain. Although S. cerevisiae
lacks an ortholog of SREBP, it seems that a potentially analogous oxygen-sensing mechanism exists in budding yeast regulated through Upc2p and Ecm22p. Marie et al.
) have observed that Upc2p and Ecm22p are localized outside of the nucleus in sterol replete conditions, but in conditions of sterol depletion localization shifts toward the nucleus. The authors suggest that the N-terminal transcription factor domain is separated from the C-terminal transmembrane domain by proteolytic cleavage and enters the nucleus to activate gene expression, analogous to SREBP regulation of cholesterol biosynthesis in mammals.
Upc2p and Ecm22p both bind a sequence motif known as the sterol regulatory element (SRE) (48
). Nearly one-third of hypoxically induced genes in S. cerevisiae
contain at least one potential Upc2p/Ecm22p binding site, suggesting that these transcription factors are major players in the adaptation to hypoxia (55
). The activation of target genes by Upc2p occurs in response to low sterol levels, which can be caused by blocks in ergosterol biosynthesis or by hypoxia. Davies and Rine (29
) observed that both Upc2p and Ecm22p require a functional version of Hap1p for basal expression of ERG2
, but when sterols are depleted Upc2p is independent of Hap1p, whereas Ecm22p still depends upon Hap1p for ERG
gene activation. ERG2
, and DAN4
are activated by Upc2p solely in response to sterol depletion whereas DAN1
respond to both sterols and heme (46
Other oxygen sensing mechanisms
An additional hypoxic regulatory pathway involving an antagonistic interaction between the Ord1p repressor and the Yap1p factor (a transcriptional activator involved in oxidative stress response) has been discovered in S. cerevisiae
and regulates both TIR1
The hypoxic response of TIR1
(both encode cell wall mannoproteins) depends on the absence of heme but is Rox1p-independent. Under aerobic conditions, Ord1p binds to the SRP1
promoter and expression is repressed. When conditions change to hypoxia, Yap1p also binds to the SRP1
promoter, counteracts the Ord1p effect and SRP1
is expressed (56
Multiple pathways involved in regulating hypoxic and anoxic gene expression in yeast may exist. Studies of several other hypoxic/anaerobic genes including SUT1
, encoding a putative Zn[II]2Cys6-transcription factor that facilitates the uptake and synthesis of sterols under hypoxic conditions (57
, encoding an isoenzyme of NAD-dependent glycerol 3-phosphate dehydrogenase (58
), and members of the seripauperine (PAU
) family, like TIR1
) have demonstrated Rox1p-independent hypoxic/anaerobic induction, but the mechanisms by which this occurs are not yet understood.
Another recently described possible mechanism of hypoxia signaling in yeast involves the mitochondrial respiratory chain, the cytochrome c oxidase and reactive oxygen species (60
). It has been shown that mitochondria from yeast, rat liver, and plants are capable of nitrite (NO2-
)-dependent nitric oxide (NO) synthesis (60
). This pathway is induced when cells experience hypoxia, and furthermore, Castello et al.
) suggest that mitochondrially produced NO functions in a signaling pathway to the nucleus by reacting with the superoxide produced by hypoxic mitochondria (67
) to form peroxynitrite (ONOO-
) that promotes protein tyrosine nitration of specific proteins that may be involved in a signaling pathway to the nucleus. Future research on this mechanism will likely uncover its specific role in hypoxia adaptation.
It seems clear that adaptation to hypoxia is a complex multi-faceted process regulated via the interaction of several different critical metabolic pathways in the cell. The major regulatory pathways discussed above are summarized in and . We now turn our attention to other fungi and discuss similarities and differences with these hypoxia adaptation mechanisms in S. cerevisiae. As many of the pathogenic fungi employ different life-styles than S. cerevisiae, it is still unclear which of these pathways involved in regulating responses to hypoxia in baker's yeast are conserved in fungi that invade mammalian hosts.
Schematic of the oxygen sensing pathways in Saccharomyces cerevisiae and Candida albicans
Hypoxia sensing mechanisms and pathways.
Candida albicans Candida albicans
is an important human fungal pathogen that causes superficial skin infections as well as deep-seated infections, suggesting that its ability to switch between normoxia and hypoxia is a major determinant of its virulence (68
). In C. albicans
little is known about mechanisms utilized by this yeast to adapt to hypoxic microenvironments. However, our current knowledge suggests that the transcriptional response to hypoxia differs significantly between C. albicans
and S. cerevisiae
in important aspects. Although both are generally referred to as facultative anaerobes, genetics studies, conditions required for anaerobic growth, and genome analyses seem to suggest that these hemiascomycota yeast respond differently to changes in oxygen levels.
First, a homologue (Rfg1p) of the S. cerevisiae
Rox1p has been identified in C. albicans
, but Rfg1p does not play a role in the regulation of hypoxic genes in this pathogenic yeast as in S. cerevisiae
(). Instead, Rfg1p is a transcriptional regulator that controls filamentous growth, and in that role, is critical for C. albicans
Second, S. cerevisiae
genes involved in glycolysis and fermentation are not stimulated by hypoxia (25
), but hypoxia induces these genes and genes involved in hyphal growth in C. albicans
while genes of oxidative metabolism are repressed (68
). During normoxic conditions the global transcription factor Efg1p regulates the expression of genes involved in glycolysis and respiration, but it has no role in controlling the expression of respiratory genes and is not required to upregulate glycolytic gene expression in hypoxia (68
). Efg1p also promotes filamentation under normoxic conditions. Recently, it was observed that under hypoxic conditions Efg1p promotes the synthesis of unsaturated fatty acids, the up-regulation of genes involved in the stress response (HSP12
) and represses filamentous growth in C. albicans
. Thus, the regulatory role of Efg1p in C. albicans
strongly depends on oxygen (68
). Transcriptional analyses observed that Efg1p is required to allow hypoxic regulation of about half of all genes that are normally regulated by hypoxia in C. albicans
. In an efg1
mutant, hypoxic upregulation (e.g. CTA1
) or downregulation (e.g. RIP1
) of several genes is abolished, and some genes, like OLE1
encoding a fatty acid desaturase, are ineffectively expressed in hypoxia. Another major function of Efg1p is to prevent hypoxic regulation of numerous genes that are not normally up- or downregulated under hypoxia (71
). Despite the fact that Efg1p is a major regulator of the hypoxic response in C. albicans
, a homozygous efg1
mutant shows no severe change in virulence in comparison to the wild-type (73
Another transcription factor in C. albicans
affected by hypoxia, Ace2p, is required for filamentation in response to hypoxic conditions. Ace2p also induces fermentative growth and represses respiration, but it is possible that the effect of Ace2p on metabolism is restricted to normal oxygen conditions. This remains to be tested (74
). Interestingly, an ace2
null mutant is almost avirulent in an immunocompetent mouse model, while there is only a low degree of attenuation in a neutropenic mouse model (75
). This may suggest that different states of the immune system may affect the development of hypoxia in vivo
i.e. the lack of neutrophils in the neutropenic model minimizes the inflammatory response and hence hypoxic microenvironments encountered by the invading fungus. This remains to be examined and confirmed.
As in S. cerevisiae
), the cell-wall proteome of C. albicans
is sensitive to changes in environmental conditions which helps the cell to adjust to harsh environments. For example, iron deprivation and hypoxic conditions affect the expression of cell-wall protein encoding genes, such as iron acquisition and iron-uptake genes i.e. RBT5
a gene encoding a predicted GPI protein involved in iron acquisition (68
). Numerous oxygen-dependent reactions in the cell are carried out by iron-containing enzymes (79
). During hypoxic conditions, there may be competition for iron by iron-containing enzymes, which might lead to an increased expression of cell-wall protein encoding genes involved in iron-acquisition and iron-uptake (80
Oxygen sensing in Candida albicans
In S. cerevisiae
it has been observed that the cell senses oxygen availability through cellular heme and sterol levels (27
). In C. albicans
, no apparent homolog of ScHAP1
exists, but in recent studies a close ortholog of S. cerevisiae
Upc2p and Ecm22p, both involved in sensing sterol depletion, has been identified. Upc2p, a transcription factor of the zinc cluster family, is an important regulator of the sterol biosynthesis and azole drug resistance in C. albicans
) (). Hoot et al.
) showed that transcriptional regulation of UPC2
expression occurs through Upc2p-dependent as well as a novel Upc2p-independent mechanism. Whether there is also a post-translational control mechanism as described for the mammalian sterol regulator SREBP (discussed in detail below) or as suggested for the Sc
Upc2p remains to be determined.
Mutants in SREBP Pathway and Tco1 are sensitive to hypoxia
Upc2p binds in vivo
to the promoters of several ergosterol biosynthesis genes and other genes involved or predicted to be involved in lipid metabolism. Znaidi et al.
) observed that up-regulation of ERG11
during hypoxia is strictly Upc2p dependent. Upc2p also binds the promoters of four genes encoding transcription factors (INO2
, and UPC2
itself). One of them, Sut1p, controls sterol uptake in S. cerevisiae
) suggesting that in C. albicans
Upc2p and Sut1p may interact in a sterol regulatory network (84
Interestingly, Upc2p also binds to the promoter of CBP1
, which was shown to encode a corticosteroid binding protein in C. albicans
). C. albicans
appears to take up steroids and possibly metabolic precursors from the host, and Upc2p seems to play a role in corticosteroid uptake from mammals and in adaptation of C. albicans
to hypoxic conditions in the host (84
). Thus, an emerging theme with studies in S. cerevisiae
and C. albicans
is the role of sterol homeostasis in adaptation to hypoxic microenvironments. This theme will also be expanded on in additional fungi discussed below with the discovery of SREBP orthologs. A summary of the known hypoxia regulation mechanisms in C. albicans
is presented in and .
Fungi with SREBP orthologs
Recently, a novel mechanism of hypoxia adaptation mediated by a highly conserved family of transcription factors, the SREBPs, was characterized in Schizosaccharomyces pombe
). S. pombe
, also called “fission yeast”, is a non-pathogenic yeast that is used as a model organism in molecular and cell biology. SREBPs are a family of endoplasmic reticulum (ER) membrane bound transcription factors first identified in mammals as regulators of cholesterol and fatty acid synthesis (88
). SREBPs contain two transmembrane segments and are inserted into ER membranes in a hairpin fashion such that the N- and C-terminal ends of the protein are in the cytosol. SREBP is synthesized as an inactive membrane-bound precursor that forms a complex with SCAP (S
rotein), a multispan membrane protein that is a component of the sterol sensor (90
). Under conditions with enough available sterols, the SREBP-SCAP complex is retained in the ER membrane through binding of SCAP to the resident ER protein Insig (93
). In sterol-depleted cells, SCAP changes its confirmation, which releases the SREBP-SCAP complex from Insig (94
). SCAP then escorts SREBP from the ER to the Golgi apparatus where SREBP is activated by two sequential proteolytic events catalyzed by site-1 and a site-2 proteases that release the N-terminal transcription factor domain from the membrane, allowing the transcription factor to enter the nucleus and direct the transcription of target genes (90
In S. pombe
apparent orthologs of SREBP (SRE1
), SCAP (SCP1
) and Insig (INS1
) have been identified and characterized. Sre1p is cleaved and activated in response to sterol depletion and hypoxia, and stimulates transcription of genes required for adaptation to hypoxia such as genes involved in heme, sphingolipid, ubiquinone, and ergosterol biosynthesis ( and ) (87
). Thus, in fission yeast, Sre1p and Scp1p appear to monitor-oxygen dependent sterol synthesis as an indirect measure of oxygen supply. Interestingly, there does not appear to be an impact of Ins1p on the SREBP pathway in fission yeast. In addition, Hughes and Espenshade (97
) recently identified another component of this pathway, Ofd1p. Ofd1p is a prolyl 4-hydroxylase- like 2-oxoglutarate-Fe(II) dioxygenase that accelerates Sre1p degradation in the presence of oxygen. The N-terminal dioxygenase domain is an oxygen sensor that regulates the activity of the C-terminal degradation domain (97
). Altogether, the SREBP pathway functions as an oxygen sensor and is required for adaptation to hypoxia in fission yeast. However, the critical function of Sre1 in allowing hypoxic adaptation and subsequent growth is not clearly defined. It seems likely that Sre1 is playing a pleiotropic role in regulating many different genes required for yeast cells to adapt and grow in hypoxia.
Schematic of the oxygen sensing pathways in Schizosaccharomyces pombe, Cryptococcus neoformans and Aspergillus fumigatus
Orthologs of the SREBP pathway were recently identified and characterized in the human fungal pathogens C. neoformans and A. fumigatus. Yet, the exact components and the mechanism behind SREBP regulation largely remain to be determined in these pathogenic fungi. Moreover, it appears that the SREBP pathway is similar in function to the Upc2p mediated pathway in S. cerevisiae and C. albicans, but the mechanisms behind the similarities and differences between these two pathways is currently not clear.
Unlike the Ascomycete yeast S. cerevisiae
and C. albicans,
the Basidiomycete yeas Cryptococcus neoformans
is generally considered an obligate aerobe. Cryptococcus
species cause the disease Cryptococcosis in both immunocompromised and apparently healthy hosts and are the most common cause of fungal meningitis (98
). C. neoformans
is primarily found in pigeon droppings and soil contaminated with avian guanos throughout the world (99
). One would speculate that these environments are relatively oxygen poor suggesting that C. neoformans
likely has evolved mechanisms to adapt to low oxygen microenvironments. In the laboratory, C. neoformans
grows optimally under atmospheric oxygen conditions (21%), but oxygen concentrations in the human brain are drastically lower than in the atmosphere and vary significantly among anatomical sites (2
). Thus, in order to establish an infection in the brain, it seems likely that C. neoformans
must adapt to reduced oxygen levels during infection. Therefore, discovering the mechanisms utilized by C. neoformans
to sense and adapt to low-oxygen conditions is an important area of research aimed towards understanding the pathobiology of this pathogenic yeast. Yet, until recently, the importance of hypoxia adaptation in C. neoformans
biology and virulence have been largely un-studied.
Recent whole-genome microarray-based transcriptional profiling of C. neoformans
in a hypoxic microenvironment has started to reveal genes and pathways regulated in response to hypoxia. Among them are genes involved in hexose uptake (sugar transporter and hexose transporter), ethanol production (pyruvate decarboxylase and alcohol dehydrogenases), and sterol metabolism (ergosterol biosynthesis genes) (100
). The possibility of fermentation being important for hypoxic growth during infection is supported by another study, where ethanol was found in cerebral tissue of rats infected with C. neoformans
). Yet the importance of fermentation pathways in this obligate aerobe's ability to cause disease and grow in hypoxic microenvironments is unknown. However, as with other yeasts we have discussed, and the filamentous mold A. fumigatus
, sterol biosynthesis and homeostasis seems to be a common mechanism regulating adaptation to low oxygen environments in fungi.
The SREBP pathway in Cryptococcus neoformans
Orthologs of SREBP (SRE1
), SCAP (SCP1
) and a Site-2-protease (STP1
) were identified and characterized in C. neoformans
). C. neoformans
appears to lack an identifiable homologue of Insig, the ER retention-protein that controls ER-to-Golgi transport of SREBP-SCAP complex in mammalian cells. This finding is consistent with S. pombe
data which suggests that Insig is not required for sterol-dependent regulation of Sre1p and Scp1p (87
). However, as in fission yeast, the SREBP pathway mediated by Sre1p and Scp1p in C. neoformans
is crucial for adaptation to hypoxia and sterol biosynthesis (). In addition, unlike in S. pombe
, Sre1p controls low-oxygen expression of genes required for two different pathways of iron uptake (SIT1
), which might be crucial for survival under hypoxic conditions. Importantly, sre1Δ
mutants fail to proliferate in host tissue, fail to cause fatal meningoencephalitis, and display hypersensitivity to the azole class of antifungal drugs ( and ) (100
). It is unclear if the virulence defect is due to deficiencies in iron homeostasis, a known virulence attribute of pathogenic fungi, or the inability of C. neoformans
to grow in low oxygen microenvironments in the absence of Sre1p. The two phenotypes are likely not mutually exclusive given the importance of iron in ergosterol biosynthesis. However, it is clear that C. neoformans
needs Sre1p activation to adapt to the host environment. Mechanisms linking ergosterol biosynthesis, iron homeostasis, and fungal virulence in this pathogenic yeast remain unknown. Identification and characterization of additional components of the SREBP pathway are likely to yield important insights into how this pathogenic yeast causes disease.
In order to identify novel Sre1p pathway components in C. neoformans
, Lee et al.
) observed that responses to cobalt chloride (CoCl2
) in C. neoformans
mimic certain aspects of hypoxia by targeting enzymes in the sterol biosynthesis pathway. CoCl2
has been widely used as a hypoxia-mimicking agent in mammalian systems (104
), but the mechanisms by which it induces hypoxia-mimicking responses are not fully understood. However, Sre1p is required for adaptation to CoCl2
in C. neoformans
. Upon CoCl2
treatment, Sre1p is likely activated in response to sterol defects caused by the inhibition of several enzymatic steps in the ergosterol biosynthetic pathway. CoCl2
treatment leads to increased levels of sterol intermediates, including the substrates of Erg25p, 4,4-dimethylfecosterol and 4-methylfecosterol, demonstrating that Sre1p regulates sterol homeostasis in response to CoCl2
-induced sterol synthesis inhibition and Sre1p activation has also been observed in S. pombe
, suggesting a conserved role for Sre1p in the adaptation to elevated levels of transition metals (103
treatment has been used to screen for pathways involved in oxygen sensing in C. neoformans
. In this context Ingavale et al.
) observed that CoCl2
sensitivity and/or oxygen sensing and adaptation processes in C. neoformans
have a complex nature. Importantly they identified several mutants with increased sensitivity to CoCl2
and they observed that most of the CoCl2
sensitive mutants are also sensitive to low oxygen concentrations. Mutants included genes involved in the sterol biosynthesis pathway such as SCP1
, SRE1, ERG5
, mutants in genes involved in mitochondrial function and energy metabolism such as H+
transporting ATP synthase, NADH:ubiquinone oxidoreductase or ATP:ADP anitporter, and various transporters and enzymes such as hexose transport related protein, seroheme synthase, amino acid transporter and myo-inositol oxygenase. The role of these genes and pathways in fungal virulence has yet to be explored, but the apparent role of the mitochondia in hypoxia adaptation in C. neoformans
echoes the recent findings in S. cerevisiae
The two-component like (Tco) system in Cryptococcus neoformans
Additional studies observed that the Sre1p pathway acts in parallel with a two-component signal transduction like pathway controlled by Tco1p in hypoxic adaptation of C. neoformans
). Tco1p is a member of a highly conserved family of fungal-specific histidine kinases. Tco1p negatively regulates the expression of melanin formation and, redundantly with Tco2p, positively regulates the HOG MAPK pathway (which is dispensable for virulence) (110
). Interestingly, it has been shown that Tco1p is required for growth under hypoxic conditions and for virulence of C. neoformans
). However, it is unclear how this pathway is involved in hypoxic adaptation and fungal virulence (). In contrast to mutants in SRE1
, the tco1Δ
mutant shows no detectable defects in the regulation of any of the known hypoxic genes ((100
), unpublished data). As a result Chun et al.
) hypothesize that the Tco1p pathway might act post-transcriptionally. However, this result may also indicate that novel pathways or altered function of existing known pathways regulated by Tco1p are involved in hypoxia adaptation. Clearly, however, these data suggest that oxygen sensing in C. neoformans
is highly complex, and likely important for virulence of this organism.
Aspergillus fumigatus A. fumigatus
is a saprophytic, obligate aerobic filamentous fungus commonly found in soil and compost piles. Its primary ecological function is to recycle carbon and nitrogen through the environment (111
). As with most fungi, it seems self-evident that these microenvironments would place significant oxygen related stress on the mold. While A. fumigatus
is responsible for a number of clinically relevant diseases, invasive pulmonary aspergillosis (IPA) is the most lethal with mortality rates ranging from 60-90% (114
). Interestingly, while IPA can be caused by several Aspergillus
species, the majority of IPA cases are caused by A. fumigatus
. This may suggest that A. fumigatus
contains unique attributes that allow it to cause disease (117
Currently, we have a limited understanding of the in vivo
growth mechanisms of A. fumigatus
during IPA (118
). Given that the lung is the primary site of infection for this mold, it may be counter-intuitive to think that low oxygen levels would be a critical component of the pathophysiology of IPA. However, during infection, A. fumigatus
causes significant damage to host tissue through invasive growth by hyphae and subsequent recruitment of immune effector cells (depending on the immune system status of the host). Thus, infection generates significant inflammation and necrosis in lung tissue that can be visualized by histopathology. These pathologic lesions also likely represent areas of poor oxygen availability to the pathogen and host. Thus, it is likely that to cause disease A. fumigatus
must adapt to hypoxic conditions.
In general, mechanisms of hypoxia adaptation in molds have gone largely unstudied. Tarrand et al.
) hypothesized that the low rate of Aspergillus
recovery from clinical material is due to adaptation by the fungus to the physiologic temperature and hypoxic milieu found in vivo
. However, recent studies with A. fumigatus
suggest that it cannot grow in anaerobic environments (121
). Interestingly, studies with the relatively non-pathogenic model mold A. nidulans
observed that while the mold could not proliferate without oxygen, ethanol fermentation was required for its long-term survival in anaerobic conditions (122
). Indeed, analyses of Aspergillus
genome sequences have revealed numerous potential fermentation pathways in these molds. Yet, as obligate aerobes, it remains unclear what function these pathways may serve in hypoxia adaptation and fungal virulence. Recent studies in our laboratory have identified ethanol fermentation during A. fumigatus
infection in a murine model of IPA indicating that fermentation may be a component of the virulence arsenal of this mold (Grahl et al.
unpublished data). However, our knowledge about the mechanisms by which A. fumigatus
, an obligate aerobe, adapts to hypoxic environments remains extremely limited.
The SREBP pathway in Aspergillus fumigatus
Recently, our laboratory identified and characterized an SREBP (Sre1p) ortholog, SrbA, in A. fumigatus
). As in C. neoformans
, SrbA is crucial for adaptation to hypoxia, mediates resistance to the azole class of antifungal drugs and is involved in sterol biosynthesis in A. fumigatus
( and ). In addition, unlike C. neoformans
, but similar to S. pombe,
transcriptional profiling of the SrbA null mutant suggested that SrbA does not appear to be involved in iron uptake or homeostasis in A. fumigatus
. However, these studies may have been limited by the type of media utilized, and direct studies regarding the role of SrbA in iron homeostasis in this pathogenic mold are ongoing.
null mutants are almost avirulent in two distinct murine models of IPA. While our results strongly suggest that the virulence defect is due to the inability of this mutant to grow in hypoxia due to the loss of hypoxia adaptation mechanisms regulated by SrbA, as with C. neoformans,
other potential hypotheses may explain the attenuation of virulence (124
). For example, SrbA plays an important role in maintenance of cell polarity in A. fumigatus
). We hypothesize that the accumulation of sterol intermediates leads to dysfunction in the formation or localization of sterol microdomains known to be required for maintaining cell polarity. Thus, the alteration of cell polarity may inhibit the ability of the SrbA mutant to cause disease. Yet, the mutant displays a normal growth rate in vitro
suggesting that the altered cell polarity does not alter growth in these conditions. Altogether, these data promote the hypothesis that hypoxia plays a key role in the pathophysiology of IPA. At the least, it is apparent that SREBPs are critical components of fungal virulence in both pathogenic yeast and molds.
So far the molecular mechanism behind SrbA regulation and activation in molds is unclear. In the yeast S. pombe
and C. neoformans
, it seems evident that Sre1p is regulated post-translationally in response to sterol biosynthesis perturbation that occurs in low oxygen environments. Indeed, Hughes et al.
) have identified 4-methyl sterols as the primary activating agent of Sre1p in S. pombe
and C. neoformans
. Thus, our finding that the SrbA null mutant in A. fumigatus
accumulates 4-methyl sterols may also suggest that these sterols are the trigger for SrbA activation in A. fumigatus
While many of the phenotypes observed in the A. fumigatus srbA mutant may suggest that SrbA is regulated in a similar manner as Sre1p in yeast, our results may also suggest an alternative model in molds. For example, despite intense bioinformatic analyses, we have been unable to identify clear homologs of SCAP or the proteases required for Sre1p activation. We have, however, identified a potential Insig1 homolog (insA) and we are currently characterizing a possible role for InsA in SREBP signaling in filamentous fungi. Yet, given the conservation of SCAP across many organisms, it is surprising that an ortholog does not appear to be present in the Aspergilli. It may be that another protein with a divergent sequence performs a similar function as SCAP, or it may suggest that a novel mechanism of SREBP regulation and activation exists in molds. Studies to examine these potential mechanisms are ongoing in our laboratory.