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Bullous impetigo due to Staphylococcus aureus is one of the most common bacterial infections of man, and its generalized form, staphylococcal scalded skin syndrome (SSSS), is a frequent manifestation of staphylococcal epidemics in neonatal nurseries. Both diseases are mediated by exfoliative toxins (ETs), which show exquisite pathologic specificity in blistering only the superficial epidermis. We show that these toxins act as serine proteases with extremely focused molecular specificity to cleave mouse and human desmoglein 1 (Dsg1) once after glutamic acid residue 381 between extracellular domains 3 and 4. Mutation of the predicted catalytically active serine to alanine completely inhibits cleavage. The mutated ETs bind specifically to Dsg1 by immunofluorescence colocalization and by coimmunoprecipitation. Thus, ETs, through specific recognition and proteolytic cleavage of one structurally critical peptide bond in an adhesion molecule, cause its dysfunction and allow S. aureus to spread under the stratum corneum, the main barrier of the skin, explaining how, although they circulate through the entire body in SSSS, they cause pathology only in the superficial epidermis.
Understanding the pathology resulting from Staphylococcus aureus infection is of great interest in medicine because of the organism’s common and increasing prevalence in humans, its growing bacterial resistance, and its ability to cause serious and life-threatening disease (1). Toxins contribute in a major way to the pathogenicity of S. aureus, as they do with many other bacteria (2).
S. aureus frequently infects the skin. In fact, the most common bacterial infection of children is impetigo, which accounts for approximately 10% of all skin problems in children (3). Of these impetigo patients, about 30% have bullous impetigo, which is caused by S. aureus strains that produce exfoliative toxins (ETs). In patients discharged from the newborn nursery, over 30% may be colonized with S. aureus, and organisms that produce ETs are the major cause of neonatal nursery outbreaks of staphylococcal disease (1, 4). Newborns, young children, and adults with renal failure and/or who are immunocompromised may develop a generalized form of bullous impetigo called staphylococcal scalded skin syndrome (SSSS). In this disease, bullae and erosions develop over a large area of the skin surface, resulting in the death of probably less than 3% of affected children but up to 60% of affected adults (5, 6).
The now-classic experiments of Melish et al. in the early 1970’s established that ET produced by S. aureus causes the blistering in bullous impetigo and SSSS (7–9). Passive transfer of the toxin to neonatal mice caused the same skin lesions seen in humans, namely a blister in the superficial living epidermis caused by separation of the keratinocytes in the granular cell layer due to splitting of the desmosomes as either a primary or secondary event (10, 11). Presumably, this type of blister allows the bacteria to spread under and circumvent the stratum corneum, a major barrier that prevents infection of the skin. Two major ETs, ETA and ETB, which share 40% identity in amino acid sequence, have been identified and cloned (12, 13). Recently, a third ET (termed ETD) that causes identical epidermal blisters has been identified (T. Yamaguchi et al., unpublished observations). In bullous impetigo, blisters occur at the site of infection with S. aureus, and are caused by local production of ET, whereas in SSSS the toxin is produced at the site of infection (not necessarily in the skin) and causes generalized blistering due to its systemic circulation. The latter disease underscores the exquisite specificity of ETs that, even when they circulate through the entire body, cause pathology only in the superficial epidermis.
The pathophysiologic basis of this specificity has been a mystery for over 30 years, even though recent crystal structure and amino acid sequences of ETA and ETB have suggested that they are “atypical” glutamate-specific serine proteases. The term “atypical” was used because some crystal structures of ETA and ETB have shown that the presumed catalytic site is not configured properly to be active, perhaps requiring activation by binding to a specific substrate or receptor (14–17). On the other hand, it has been argued that the toxicity of ETs may not be as serine proteases at all (e.g., data has suggested that these ETs are poorly inhibited by serine protease inhibitors), but as superantigens or through less-direct mechanisms such as release of proteases by the epidermis (reviewed in refs. 1, 18). Furthermore, until very recently, proteolysis of a relevant biological target had not been demonstrated.
Very recently, we identified a relevant substrate of ETA, ETB, and ETD to be desmoglein 1 (Dsg1), a transmembrane glycoprotein of desmosomes in the cadherin gene superfamily (19, 20) (T. Yamaguchi et al., unpublished observations). Dsg1, but not the closely related Dsg3 or E-cadherin, is cleaved by ETs. Furthermore, Dsg1 is a relevant substrate because antibodies in the autoimmune disease pemphigus foliaceus(PF) target Dsg1 and cause clinical and histologic blisters in mouse and man identical to those seen in bullous impetigo and SSSS. These data imply that targeting of Dsg1 can result in the pathology characteristic of bullous impetigo and SSSS.
Here we demonstrate that ETA, ETB, and ETD act as glutamic acid–specific serine proteases with unusually focused specificity that results in a single cleavage of Dsg1, leading to its functional inactivation. The pathophysiology of bullous impetigo and SSSS can thus be attributed to hydrolysis of a single peptide bond, presumably in a functionally critical area in Dsg1.
The expressed proteins, vectors, and their hosts are summarized in Table Table1.1. Shuttle vector pCE104, containing ETA and ETA Cmu, was from Patrick Schlievert (Department of Microbiology, University of Minnesota Medical School, Minneapolis, Minnesota, USA) (14). ETA Amu was constructed from these vectors with the QuikChange Site-Directed Mutagenesis Kit (Stratagene, La Jolla, California, USA). ETB Amu was cloned by PCR using pCE104-ETB (20) as a template. PCR was also used to add nucleotides encoding peptide tags, V5His (Invitrogen Corp., Carlsbad, California, USA) or 3X FLAG (Sigma-Aldrich, St. Louis, Missouri, USA), to the 3′ end of these ET constructs. ETA-V5His, ETA Cmu–V5His, ETA Amu–V5His, ETB-V5His, ETB–3X FLAG, and ETB Amu–V5His were subcloned into the HindIII and EcoRI sites of pCE104. DNA was transformed into the S. aureus strain RN4220 (provided by Patrick Schlievert) via electropolation. The supernatant from RN4220 transformed with these plasmids was precipitated with 85% ammonium sulfate. Precipitated ETs were dialyzed against PBS with 1 mM CaCl2 (PBS-Ca). His-tagged ETs were purified on Ni-NTA columns (QIAGEN Inc., Valencia, California, USA) using the manufacturer’s procedure and then dialyzed against PBS-Ca. ET concentrations were estimated with a protein assay kit from Bio-Rad Laboratories Inc. (Hercules, California, USA).
ETD was cloned by PCR from a patient sample (T. Yamaguchi et al., unpublished data), and ETD Amu was cloned by PCR mutagenesis. The amplified DNA fragments were cloned into pQE70 in order to express the fusion protein with a 6xHis tag sequence on the carboxy terminus in E. coli. The recombinant proteins were purified using Ni-NTA resin according to the manufacturer’s protocol (QIAGEN Inc.).
For comparison of mutant to wild-type ETs (see Figure Figure2),2), the supernatants from transformed RN4220 staphylococci were used, with the amount of ETs normalized by Coomassie blue staining of SDS-PAGE gels in which the ETs were the major band and accounted for over 90% of the total protein.
HaCaT cell keratinocytes cultured in DMEM with 10% FBS were transduced with recombinant adenovirus vectors Ax-mDsg1F and Ax-mDsg3F (20), encoding mouse Dsg1 and Dsg3, respectively, with carboxy-terminal FLAG tags (Table (Table1).1). After 24 hours, the cells were incubated with recombinant ETA, ETB, or ETD in culture media for 10 minutes. Then the cells were washed with PBS-Ca, extracted, and used for immunoprecipitation or immunoblotting.
The entire extracellular domain of human or mouse recombinant Dsg1 with an E tag (hDsg1E and mDsg1E) on the carboxyl terminus was produced as a secreted protein by baculovirus, as previously described (21). (These constructs also contained a His tag on the carboxy terminus.) Approximately 1 μg of mouse or human Dsg1 purified with a TALON (BD Biosciences Clontech, San Jose, California, USA) or E-tag column (Amersham Biosciences Inc., Piscataway, New Jersey, USA) was incubated with recombinant ETA, ETB, or ETD in Tris-buffered saline with 1 mM CaCl (TBS-Ca) for 1 hour at 37°C. The digested samples were subjected to SDS-PAGE, transferred to PVDF membranes, and stained using Coomassie brilliant blue. Stained bands were cut out and sequenced by Edman degradation at the Protein Microchemistry Facility of The Wistar Institute (Philadelphia, Pennsylvania, USA).
Anti–E-tag mouse monoclonal antibody conjugated with horseradish peroxidase (HRP; Amersham Biosciences Inc.), anti–V5-tag mouse monoclonal antibody (Invitrogen Corp.), anti–His-tag mouse monoclonal antibody (QIAGEN Inc.), anti–FLAG-tag mouse monoclonal antibody (M2; Sigma-Aldrich), anti-ETA sheep polyclonal antibody (Toxin Technology Inc., Sarasota, Florida, USA), anti-ETD rabbit polyclonal antibody (T. Yamaguchi, unpublished observations), and PF serum (anti-Dsg1) were used for immunoblotting and immunohistochemistry. HRP-conjugated anti-IgG antibodies of the appropriate specificity (Bio-Rad Laboratories Inc.) were used for immunoblotting. Anti-human antibody conjugated with Alexa Fluor 495 and anti-mouse antibody conjugated with Alexa Fluor 590 (Molecular Probes Inc., Eugene, Oregon, USA) were used for immunohistochemistry.
Mouse tail or paw skin was incubated in DMEM at a ratio of 1:1 with 10% FBS and ETA Amu–V5His (~83 μM) in PBS-Ca at 4°C for 12 hours and then cryosectioned. After being fixed with 4% paraformaldehyde in PBS-Ca, specimens were blocked with 1% BSA in PBS-Ca. Blocked specimen was incubated with anti-V5 antibody followed by anti-mouse antibody conjugated with Alexa Fluor 590, and then stained with PF serum followed by anti-human antibody conjugated with Alexa Fluor 495. Stained sections were photographed using confocal microscopy (MRC 1024; Bio-Rad Laboratories Inc.). For controls, skin was first incubated with wild-type ETA or an irrelevant toxin (staphylococcal enterotoxin B with a V5 tag), then stained with PF serum or anti-V5 antibody, respectively. These controls showed no staining (not shown).
After incubation with ETs, adenovirus-infected cells were extracted with 1% Triton X-100 in TBS-Ca with protease inhibitors (2 μg/ml aprotinin, 2 μg/ml leupeptin, and 1 mM PMSF) for immunoprecipitation. Supernatants of High Five insect cells (Invitrogen Corp.) transduced with baculovirus encoding hDsg1E were incubated with ETs, then used directly for immunoprecipitation. FLAG-tagged proteins were precipitated with anti-FLAG agarose (Sigma-Aldrich), and E-tagged proteins were precipitated with anti–E-tag Sepharose (Amersham Biosciences Inc.) at 4°C for 1 hour. Immunoprecipitates were washed ten times with 1% Triton X-100 in TBS-Ca, then eluted with Laemmli sample buffer at 100°C.
Cell extracts or immunoprecipitates in Laemmli sample buffer were separated by 4–20% or 10% Tris-glycine SDA-PAGE (Bio-Rad Laboratories Inc. or Invitrogen Corp.), then transferred to nitrocellulose sheets (Trans-Blot; Bio-Rad Laboratories Inc.). The sheets were incubated for 1 hour in blocking buffer (5% fat-free milk powder in PBS). The first antibody, diluted in blocking buffer, was applied for 1 hour at room temperature. After two washes with 0.1% Tween 20 in PBS, the sheets were incubated with HRP-conjugated secondary antibody diluted in blocking buffer. In some experiments, only one antibody, HRP-conjugated anti-ETA, was used. After the blots were washed, the signals were detected with chemiluminescence (ECL or ECL Plus, Amersham Biosciences Inc.).
Previous studies of proteolysis of Dsg1 by ETs identified only a small carboxy-terminal fragment, leaving the extent of degradation uncertain. To determine whether there is one specific cleavage site as opposed to more general proteolytic degradation, the extracellular domain of human Dsg1, containing an E tag (hDsg1E) on the carboxy terminus, was purified and cleavage was characterized by SDS-PAGE and amino-terminal sequence analysis. hDsg1E was produced by baculovirus in High Five insect cells (21). The recombinant protein was isolated from insect cell supernatant with anti–E-tag Sepharose and elution with excess E peptide. Coomassie blue staining of the peptide-eluted material resolved by SDS-PAGE (Figure (Figure1a,1a, left) indicates a closely spaced doublet at the predicted molecular weight of 84 kDa. The isolated hDsg1E was incubated for 1 hour with ETA at 37°C, and the products were separated by SDS-PAGE (Figure (Figure1a,1a, right). Two major bands of approximately 50 kDa (arrow marked 1) and 34 kDa (filled arrowhead) were detected by Coomassie blue staining, suggesting that hDsg1E was cleaved at a single site. Immunoblotting with anti–E-tag antibodies of hDsg1E digests identified the 34-kDa band as the carboxy-terminal fragment (Figure (Figure1b).1b). Amino terminal peptide sequencing of this fragment shown in Figure Figure1a1a (right side, arrowhead) was then used to determine the exact cleavage site, which was after glutamic acid residue 381 (as counted from the initiating methionine of hDsg1) (Figure (Figure1e).1e). A similar study showed that ETA cleaved mouse Dsg1 at the same site (Figure (Figure11e).
To determine the site of cleavage by ETB and ETD in hDsg1, we incubated unpurified hDsg1E (obtained directly from baculovirus supernatant) with these ETs, then purified the carboxy terminus with anti–E-tag Sepharose. Coomassie blue staining of the resulting purified carboxy-cleavage fragments separated on SDS-PAGE is shown in Figure Figure1c.1c. Amino-terminal peptide sequencing of these fragments indicated that the ETB and ETD cleavage site in Dsg1 was identical to that produced by ETA (Figure (Figure1e).1e). These data are consistent with structural models that suggest that ETA and ETB might cleave a substrate after a glutamic acid residue.
Amino terminal sequence analysis of the slower migrating 50-kDa band formed by cleavage of hDsg1E (Figure (Figure1a,1a, arrow marked 1) revealed the amino terminus of hDsg1E lacking the signal peptide (which was presumably processed by the insect cells) but still containing the propeptide (Figure (Figure1d).1d). Sequencing of the band shown immediately below the 50-kDa band (Figure (Figure1a,1a, arrow marked 2) indicated that it was the amino terminus of the hDsg1E mature protein (Figure (Figure1d).1d). These data show that the signal peptide of hDsg1E produced by baculovirus in insect cells is properly processed, and confirm that the sequence previously predicted by computer modeling to be the signal peptide in hDsg1 (Figure (Figure1d,1d, shown in green) is correct. The data also show that the proprotein produced by baculovirus in insect cells is not efficiently processed. However, both the precursor and mature proteins are efficiently cleaved by ETA at the same site.
Taken together, the data in Figure Figure11 demonstrate that ETA, ETB, and ETD cleave hDsg1 at the same site, and that ETA cleaves mDsg1 at the homologous site. These ETs are known not to cleave the closely related Dsg3 (19, 20). Sequence alignment of human and mouse Dsg1 and Dsg3 (Figure (Figure1e)1e) indicated marked homology (17 of 18 identical residues) of mouse and human Dsg1, but divergence of Dsg3, around the cleavage site.
The inference from structural studies of ETA and ETB is that the serine residue at position 195 in ETA and 186 in ETB corresponds to the catalytically active serine 195 of chymotrypsin. Furthermore, like chymotrypsin, ETA and ETB have a functional catalytic triad consisting of serine 195/186/195, histidine 72/65/57, and aspartic acid 120/114/102 (ETA/ETB/chymotrypsin numbering; subsequent numbering will be for chymotrypsin only). To demonstrate that this serine is critical in the cleavage of hDsg1, it was mutated to a cysteine (resultant mutant ETA Cmu). Incubation of ETA Cmu with Dsg1 at 37°C for 1 hour demonstrated a markedly decreased rate of cleavage compared with wild-type ETA (Figure (Figure2).2). Assuming this activity was likely mediated by the cysteine sulfhydryl group, similar to what has been found in a similar mutant of trypsin (22), we mutated serine 195 to alanine (ETA Amu). The ETA Amu did not cleave Dsg1 (Figure (Figure2).2). We similarly showed that mutation of serine 195 to alanine in ETB and ETD inhibited cleavage of Dsg1 (Figure (Figure22).
The observations that substitution of serine 195 with both cysteine and alanine inhibit cleavage, and that the mutant ETs still specifically bind Dsg1 (see below), demonstrate that serine 195 is necessary for efficient catalytic cleavage of Dsg1.
Crystal structural studies of ETA have suggested that it may be an inactive enzyme due to an inappropriate alignment of certain residues forming the active site. It has been postulated that as a consequence, ETA may have to bind to its specific substrate or to a receptor in order to become catalytic (14–16, 23). (However, for an opposing view, see ref. 17.) In SSSS and in mouse models of SSSS, ETs diffuse through the entire body, yet have exquisite specificity in causing pathology (e.g., blisters) only in the superficial epidermis. We have hypothesized that this specificity is due to specific recognition and cleavage of a single target, Dsg1.
If ETA binds to Dsg1, and that binding does not require the catalytic serine, then ETA Amu should be a competitive inhibitor of wild-type ETA. Establishing the ability of ETA Amu to protect Dsg1 from cleavage by ETA would also provide an estimate of the dissociation constant (Kd) for the reaction. To determine the Kd for the interaction between ETA Amu and Dsg1, Dsg1 was incubated with increasing concentrations of ETA Amu, with ETA Amu always in large excess of Dsg1. Free Dsg1 was evaluated by relatively rapid treatment with wild-type ETA and by using SDS-PAGE to estimate the fraction cleaved and the fraction protected from cleavage (Figure (Figure3).3). At concentrations of 13 μM and above, ETA Amu mostly inhibited cleavage, but at concentrations of 4 μM and below, it did not. Approximately half of the Dsg1 was observed cleaved at an ETA Amu concentration of 8 μM, allowing Kd to be roughly estimated as follows:
The magnitude of this Kd is within the range of a hydrolytic reaction whose specificity is due to relatively strong binding in the catalytic site with a relatively low Km, but is probably not consistent with strong binding to an site outside the substrate binding site.
We further showed that mutant ETA binds the epidermis where it causes a blister. This was demonstrated by incubating mouse skin with ETA Amu with a V5 epitope tag on the carboxy terminus at concentrations in excess of Kd. Immunofluorescence with antibodies against the V5 tag showed binding of ETA Amu to epidermis in a pattern identical to that of Dsg1 (Figure (Figure44).
Finally, we confirmed by coimmunoprecipitation that ETs bind Dsg1. Incubation of active ETs with Dsg1 showed coprecipitation that quickly decreased with time as cleavage progressed (Figure (Figure5a).5a). The rapid change in the ability to coprecipitate ETA with Dsg1 indicates that ETA dissociates from Dsg1 after hydrolysis of the targeted peptide bond, consistent with enzyme recycling. Supporting this conclusion are studies with ETA Cmu, which hydrolyzes Dsg1 at a much slower rate. Consistent with the slower cleavage rate, coprecipitation of ETA Cmu with Dsg1 was observed over a longer time, but still decreased with increasing hydrolysis (Figure (Figure5b).5b). Finally, ETA Amu, which does not cleave Dsg1 at all, showed increased binding with time.
To show specificity of binding in these studies, we also incubated Dsg3 with ETs and showed that ETs did not cleave or bind to Dsg3, which is highly homologous in amino acid sequence to Dsg1 (Figure (Figure55c).
Previous studies have suggested various possible sites and mechanisms of action of ETs, such as binding to gangliosides, causing release of proteases by keratinocytes; acting as superantigens in stimulating the skin’s immune system; and acting as lipases (reviewed in ref. 1). However, recent inferences from crystal structures of ETA and ETB suggest that they might be atypical serine proteases (14–17). These ETs have a structural homology to the chymotrypsin family of serine proteases. The presumptive active site contains the classic catalytic triad of serine 195, histidine 57, and aspartic acid 102. In addition, homology to the Streptomyces griseus protease Glu-SGP suggests that ETA and ETB cleave after a glutamic acid (or possibly aspartic acid) residue that would be stabilized in the active site by histidine 213, threonine 190, and lysine 216. However, the ETs are atypical because in ETA, and possibly ETB, the oxyanion hole, which helps to stabilize the transitional-state complex of catalysis, is not properly formed. This is because, as indicated by crystal structures, the peptide bond between proline 192 and glycine 193 is flipped 180° relative to typical serine proteases. This observation has led to speculation proposing the requirement for interaction with a specific substrate or receptor that would impart the relatively small energy necessary to flip this bond.
Despite these predictions, only one protein substrate, melanocyte-stimulating hormone, was reported to be cleaved by ETs until recently, although an ester substrate was reported (24, 25). The biological significance of this protein substrate, however, was not apparent.
Recently we showed that Dsg1 is cleaved by ETA and ETB (19, 20). Here we determine the molecular mechanism of that cleavage and of its exquisite specificity. The ETs (ETA, ETB, and ETD) specifically bind, and consistent with the predictions from amino acid sequence and crystal structure, act as glutamic acid–specific serine proteases to cleave Dsg1 at a unique site. These data are also consistent with previous findings of differential accumulation of ETA in newborn mouse skin compared with blood and other tissues (26).
Proteolysis of this one peptide bond leading to dysfunction of Dsg1 and the desmosome would explain the pathophysiology of blister formation in bullous impetigo and SSSS (see below). It is therefore likely that this peptide bond is critically important to the proper function of Dsg1. Its site in relation to the domain structure of Dsg1 is shown in Figure Figure6.6. Interestingly, the ETs cleave at the border between extracellular cadherin domains (ECs) 3 and 4, just toward the carboxy terminal from one of the predicted calcium-binding domains in EC3. Although three-dimensional structures of desmogleins have not been solved, there is marked homology in both calcium-binding sites and ECs between E- and N-cadherins and Dsg1. Structural studies of E- and N-cadherin have suggested that the border between ECs, through calcium binding, stabilizes the rigidity of the molecule and fixes its orientation, and is critical for function (27–31). The results we present here suggest that this border between ECs in Dsg1 is also critical for their proper function, since the cleavage of one peptide bond in this region causes dramatic dysfunction of this desmosomal cadherin.
In bullous impetigo and SSSS, blisters occur in the superficial epidermis from loss of keratinocyte adhesion in the granular layer. Strikingly, an autoantibody-mediated disease, PF, has very similar histopathology to that seen in bullous impetigo and SSSS. PF is caused by anti-Dsg1 autoantibodies (32–34).
Although these antibodies are thought to inactivate Dsg1, which is found throughout the epidermis and in mucous membranes, the blister occurs only in the superficial epidermis. This blister localization has been explained by the “desmoglein compensation hypothesis” (35). This hypothesis states that in areas of epithelium where both Dsg3 and Dsg1 are expressed, a spontaneous blister will not occur when anti-Dsg1 antibodies inactivate Dsg1, because Dsg3 can compensate. However, if only Dsg1 is present, a blister will occur. This hypothesis has been validated both by clinical observation and experimentally. In mucous membranes, both Dsg1 and Dsg3 are found throughout the epithelia; therefore, no blisters are seen in PF, even though anti-Dsg1 antibodies bind to mucous membranes. In epidermis, Dsg1 is found throughout, but Dsg3 is only in the deep epidermis. Therefore, PF antibodies cause only superficial blisters where Dsg1 is not compensated for by Dsg3. Similarly, mothers with PF passively transfer anti-Dsg1 antibodies to their neonates; however, these neonates do not develop PF because neonatal skin, unlike adult skin, expresses Dsg3 throughout all layers (36).
Experimental evidence for the desmoglein compensation hypothesis has been obtained in the neonatal mouse model of PF in which passively transferred antibodies from PF patients cause clinically and histologically typical disease (35). Normal neonatal mice that have Dsg3 in the deep epidermis (similar to adult human epidermis) and throughout the oral mucous membranes develop only superficial epidermal blisters when injected with PF IgG, but Dsg3 knockout mice, which have no Dsg3 to compensate, develop blisters in the deep epidermis and in oral mucous membranes when similarly injected. Furthermore, mice that express Dsg3 in the superficial epidermis (from a transgene containing Dsg3 cDNA driven off an involucrin promoter) are not susceptible to blistering from injected PF IgG (36). These data provide an explanation for antibody inactivation of Dsg1 resulting in blisters only in the superficial epidermis.
ETs cause blisters with pathology identical to those occurring in PF. Although ETs circulate throughout the body in SSSS, as do anti-Dsg1 antibodies in PF, blisters occur only in the superficial epidermis, not in the deep epidermis or in mucous membranes, identical to the findings in PF. Such identical pathology can be explained by the loss of function of Dsg1 caused by antibodies in the case of PF, and by ET cleavage in the case of SSSS or bullous impetigo. Loss of function of Dsg1 by cleavage with ETs is also consistent with previous immunofluorescence experiments in which ETs cause cellular internalization and loss of cell surface staining of Dsg1 (19).
A major physiologic function of skin is to provide a barrier against infection. Much of that barrier resides in the stratum corneum. S. aureus, through the use of ETs, has evolved an efficient and extremely focused mechanism of proliferating and spreading under that barrier. Once introduced, the bacteria can spread efficiently by using ET to produce a cleavage plane right under the stratum corneum. To do so, the bacterium has developed a toxin that specifically binds and cleaves a molecule that is critical to adhesion in this area and cleaves it at a specific site that destroys its function.
We thank Michael Plotnik for helpful discussions. This work was supported by grants from NIH and a Grant-in-Aid for Scientific Research from the Ministry of Education, Science, and Culture of Japan.
Conflict of interest: No conflict of interest has been declared.
Nonstandard abbreviations used: exfoliative toxin (ET); staphylococcal scalded skin syndrome (SSSS); desmoglein 1 (Dsg1); Tris-buffered saline (TBS); horseradish peroxidase (HRP); pemphigus foliaceus(PF); extracellular cadherin domain (EC).