Superantigens (SAgs) are microbial toxins that bind to both TCR β-chain variable domains (Vβs) and MHC class II molecules, resulting in the activation of T cells in a Vβ-specific manner. It is now well established that different isoforms of MHC II molecules can play a significant role in the immune response to bacterial SAgs. In this work, using directed mutational studies in conjunction with functional analyses, we provide a complete functional map of the low-affinity MHC II α-chain binding interface of the SAg streptococcal pyrogenic exotoxin C (SpeC) and identify a functional epitope in the β-barrel domain that is required for the activation of T cells. Using cell lines that exclusively express individual MHC II isoforms, our studies provide a molecular basis for the selectivity of SpeC-MHC II recognition, and provide one mechanism by how SAgs are capable of distinguishing between different MHC II alleles.
Superantigens (SAgs)3 are microbial toxins that function to simultaneously engage the lateral surfaces of MHC class II molecules (1, 2, 3, 4, 5, 6, 7, 8) and TCR β-chain variable regions (Vβs) (9, 10, 11, 12, 13, 14, 15). The unconventional contacts that SAgs make with these two adaptive immune receptors allows for the activation of large numbers of T cells that initially expand in a Vβ-specific manner (16). In severe cases of SAg exposure the ensuing cytokine “storm” can result in the toxic shock syndrome (17, 18), and SAgs have also been implicated in a variety of other immune-mediated diseases (19, 20, 21, 22). Despite engagement of MHC II as one defining feature of SAgs and a wealth of structural information regarding how SAgs bind MHC II, there is generally little data to indicate the molecular requirements for MHC II discrimination.
Bacterial genome sequencing projects have revealed that there are a large number of genetically distinct SAgs, of which there are >30 identified serotypes (23), that can be classified into at least five distinct evolutionary groups (I–V) (18, 24, 25). A phylogenetic tree showing this classification scheme has been recently published (24). Pyrogenic toxin SAgs include the toxic shock syndrome toxin-1 (TSST-1) and numerous staphylococcal enterotoxin serotypes produced by Staphylococcus aureus, as well as multiple streptococcal pyrogenic exotoxin serotypes produced by Streptococcus pyogenes and related β-hemolytic streptococci (18). Although these toxins all have a generally conserved structure including an N-terminal β-barrel domain and a larger C-terminal β-grasp domain (26), each distinct evolutionary group likely engages host receptors in structurally and functionally distinct ways.
The TCR Vβ binding interface on the surface of SAgs exists in a relatively conserved position located in a groove between the β-barrel domain and the β-grasp domain and invariably involves the SAg N-terminal α-helix. However, each characterized SAg evolutionary group demonstrates unique TCR Vβ binding contacts and orientations and, thus, each group results in altered T cell activation complexes (25).
Engagement of MHC II by SAgs is more variable than Vβ engagement and can occur through at least three clearly distinct modes. For example, TSST-1 (the only group I SAg) binds the MHC II α-chain (MHCα) through the TSST-1 N-terminal β-barrel domain in a relatively low-affinity (KD ∼ 10−5) interaction that also engages the antigenic peptide and makes contacts within the β1 domain of the MHC II β-chain (MHCβ) (3) (Fig. 1⇓). Thus, TSST-1 engagement of MHC II can be strongly influenced by the antigenic peptide (27). Group II SAgs such as staphylococcal enterotoxin B (SEB) and staphylococcal enterotoxin C3 (SEC3), as well as the group III SAg staphylococcal enterotoxin A (SEA), each engage MHCα similarly, although these toxins bind to a more lateral region on MHCα compared with TSST-1 and, consequently, these interactions are peptide independent (2, 4, 8) (Fig. 1⇓). Currently, there is no structural data to indicate how the group IV or the group V SAg engages MHCα. In addition to the low-affinity MHCα binding, group III (7), group IV (6), and group V (5) SAgs are known to bind MHCβ in an essentially conserved, relatively high-affinity (KD ∼ 10−7 M) zinc-dependent manner that occurs through the β-barrel domain located on the opposing face of the SAg (Fig. 1⇓). The high-affinity MHCβ interaction acts by coordinating a zinc ion with three conserved SAg amino acids, and the zinc ion is also coordinated by a conserved amino acid on the polymorphic β-chain (βHis81). Mutations in any of the four residues that coordinate zinc severely disrupt the activity of the SAg (28, 29, 30, 31, 32, 33, 34). Although MHCβ is highly polymorphic and much of the buried surface with the MHC β-chain is mediated by the antigenic peptide, this binding arrangement targets conservatively substituted MHCβ residues and engages the N terminus of the peptide, which is also conformationally conserved (5). Some SAgs such as SEA have been shown to cross-link MHC II molecules by binding to both MHCα and MHCβ (28, 35, 36) (Fig. 1⇓).
It is now well established that MHC II discrimination by SAgs can play a profound role in both the magnitude of the immune response and the clinical outcome of severe invasive streptococcal infections (37, 38, 39, 40, 41, 42, 43, 44). However, the molecular basis by which a particular SAg binds preferentially to certain MHC II molecules but poorly recognizes others is not well understood. To understand why SAgs preferentially engage certain MHC II molecules and to further understand receptor engagement by the group IV SAgs, we have mutated the molecular surface of streptococcal pyrogenic exotoxin C (SpeC) predicted to engage MHCα. Our findings provide the “functional epitope” on the SpeC molecular surface for engagement of different MHCα isoforms and, based on modeled complexes, we provide a molecular basis for SpeC-MHC II discrimination.
Materials and Methods
Standard DNA manipulations were performed as described (45) using enzymes supplied from New England Biolabs in accordance with the manufacturer’s instructions. Oligonucleotides were obtained from Invitrogen. PCRs were performed in a Peltier thermocycler (MJ Research) with Vent DNA polymerase (Invitrogen), and PCR products were purified using the QIAquick PCR purification kit (Qiagen). All cloned PCR products were sequenced in their entirety at the John P. Robarts Research Institute Sequencing Facility (London, Ontario, Canada) to ensure correct mutations and PCR fidelity. Escherichia coli was cultured aerobically in Luria Bertani broth (Difco) at 37°C, and solid medium was obtained by the addition of 1.5% (w/v) Bacto agar (Difco). Kanamycin (50 μg/ml) was used as a selective agent as required. All reagents were made with water purified through a Milli-Q water purification system (Millipore).
Cloning and expression of the various SpeC proteins (46, 47, 48) were performed using the modified E. coli expression vector pET41a::TEV, where the pET41a (Novagen) enterokinase cleavage site (DDDDK) is replaced with the tobacco etch virus (TEV) protease cleavage site (ENLYFQG) (49). Each SpeC mutant was generated using an overlapping megaprimer PCR method with oligonucleotides that incorporated the desired single-site mutation. SpeC proteins were expressed from E. coli BL21 (DE3) (Novagen) purified by Ni2+ column chromatography, and the purification tags were removed with autoinactivation-resistant His7::TEV as described (50). All SpeC proteins were purified to apparent homogeneity as determined by SDS-PAGE (data not shown). Key mutant proteins lacking functional activity were examined by circular dichroism analysis to confirm that the point mutations did not induce any gross structural deviations in the proteins (data not shown).
LG-2 aggregation assay
The B lymphoid cell line LG-2 was used in cell aggregation experiments (46) where the cells (100,000/ml) were suspended in R10 medium (RPMI 1640 (Invitrogen) supplemented with 10% FCS (Sigma-Aldrich), 100 μg/ml streptomycin (HyClone), 100 U/ml penicillin (HyClone), 2 mM l-glutamine (HyClone), 1 mM MEM sodium pyruvate (HyClone), 100 μM nonessential amino acid (HyClone), and 25 mM HEPES (pH 7.2) (BioShop)) and plated into each well of a 96-well plate. Afterward, each SpeC protein (1 μg/ml) was added and aggregation was monitored using an inverted microscope at various time points. The reversibility of the high-affinity MHC II binding site (51) was tested by the addition of 1 mM EDTA after 2 h to chelate divalent cations and then by the addition of 2 mM ZnSO4 after 4 h. Results were assessed as the number of cells in clumps as a percentage of the total number of cells in the field of view at ×100 original magnification.
Functional mapping of the MHCα binding interface of SpeC using Vβ2.1+ Jurkat T cells
Vβ2+ T cells are the major target of SpeC (46). Thus, we used the Jurkat T cell line eJRT3-2.1 engineered to express the Vβ2.1 chain used in the SpeC-Vβ2.1 complex (13), which pairs with the endogenous TCR α1-chain variable region (Vα1). APCs included the B lymphoid cell line LG-2, which is homozygous for the expression of HLA-DR1 (DRA*0101/DRB1*0101), HLA-DQ5 (DQA1*010101/DQB*05010101) and HLA-DP3 (DPA1*010301/DPB1*0301) (52), or the type II bare lymphocyte syndrome (BLS) B cells, which exclusively express HLA-DR1 (DRA1*0101/DRB1*0101), HLA-DR4 (DRA1*0101/DRB1*0401), or HLA-DQ2α3β (DQA1*0501/DQB1*0302) (42
The quaternary model of the SpeC-mediated T cell activation complex was constructed by superimposing the crystal structure of SpeC-Vβ2.1 (Protein Data Bank code 1KTK) (13) with the SEC3-HLA-DR1 complex (Protein Data Bank code 1JWM) (4) to orientate the low-affinity MHC class II interaction. The high-affinity MHC II interaction was oriented to SpeC by superimposing the SpeC-HLA-DR2a complex (Protein Data Bank code 1HQR) (6), and the TCR α-chain was oriented from a typical TCR-MHC II interaction (Protein Data Bank code 1FYT) (53).
Bar graphs are shown as mean ± SEM and represent 3–10 separate experiments as indicated. Statistical analyses for comparing mutant proteins with the wild-type proteins were performed using one-way ANOVA with Dunnett’s multiple comparison test (GraphPad Prism 4). Differences were considered significant when p < 0.05.
Generation of the SpeC mutants
Previous work has shown that SpeC is able to aggregate the B lymphoid cell line LG-2, and that this aggregation phenotype was attributed to the ability of SpeC to form zinc-mediated homodimers that bind adjacent MHC II molecules through the high-affinity interaction present on each monomer (46). From the crystal structure of SpeC, the dimer interface occupied the generic, low-affinity MHC II domain and thus precluded the low-affinity interaction (47). However, other work using limited mutational analysis has shown that SpeC likely possesses an alternative MHC II binding interface (29, 48) analogous to the structurally characterized low-affinity interfaces of SEA, SEB and SEC3 (2, 4, 8). Thus, to resolve the issue regarding the presence or absence of a potential low-affinity MHC II binding interface and to understand the molecular basis by which SpeC binds MHC II through this putative interface, we performed alanine-scanning mutagenesis of all SpeC residues within the β-barrel domain that could potentially contact MHC II. These mutations were initially based on the four structurally characterized SAg/low-affinity MHC II interactions including TSST-1/HLA-DR1 (3), SEB/HLA-DR1 (2), SEAD227A/HLA-DR1 (8), and SEC3/HLA-DR1 (4). A total of 20 mutations were engineered that cover 2,192 Å (2) of the SpeC surface, as well as two additional control mutations located within the characterized zinc-mediated, high-affinity MHCβ (SpeCD203A) and TCR (SpeCY15A) interfaces (6, 13), each of which are known to disrupt these respective interactions (29, 49).
LG-2 cell aggregation by the SpeC mutants is indicative of multiple binding interfaces on SpeC
We first confirmed the ability of wild-type SpeC to aggregate the LG-2 B lymphoid cell line (46), which is homozygous for the expressions of HLA-DR1, HLA-DQ5, and HLA-DP2 (52). LG-2 cells aggregated upon the addition of staphylococcal enterotoxin E (SEE), a SAg containing both the high-affinity and low-affinity MHC II binding interfaces, whereas cells treated in parallel with streptococcal pyrogenic exotoxin A (SpeA), a streptococcal SAg containing only the low-affinity MHC II binding interface, did not (Fig. 2⇓A). As expected (46), SpeC aggregated LG-2 cells in a similar manner to that of SEE (Fig. 2⇓A). The nature of this aggregation was zinc dependent because the chelation of divalent cations by the addition of EDTA disrupted aggregation, which was reversible upon the addition of excess zinc (Fig. 2⇓B). The aggregation phenotype was disrupted by an alanine point mutation in the control high-affinity interface mutant (at SpeC position Asp203), while the control TCR interface mutation (at SpeC position Tyr15) predictably did not disrupt the phenotype (Fig. 2⇓C). Of the 20 mutations within the putative low-affinity interface, alanine substitutions at positions Tyr50, Tyr76, and Tyr87 each significantly disrupted the aggregation phenotype (Fig. 2⇓C). These data suggest that there are two independent interfaces on SpeC responsible for the LG-2 cell aggregation phenotype, one that is represented by the zinc-dependent, high-affinity MHC II interface (6, 29), and a second within the β-barrel domain that is consistent with characterized low-affinity MHC II interfaces (2, 3, 4, 8).
Mutations within the putative low-affinity MHC II binding interface of SpeC impair T cell activation
Because the major targets of SpeC are T cells expressing the Vβ2 TCR (46, 49), we monitored the activation of the engineered Vβ2.1+ Jurkat T cell line eJRT3-2.1 (49) in the presence of LG-2 cells by the production of IL-2 and the phosphorylation of ERK-1/2 in response to the various SpeC mutants (Fig. 3⇓). Consistent with the LG-2 aggregation data, point mutations at Tyr50 and Tyr87 severely impaired the ability to activate T cells (Fig. 3⇓A). Mutations at Tyr76, Ile77, and Tyr85 showed an intermediate decrease in activity, whereas mutations at Thr36 and Asp183 produced mild but significant reductions in activity. The remainder of the mutants showed little to no reductions in activity. The control mutants SpeCY15A and SpeCD203A, as well as the additional double mutant SpeCY87A/D203A, behaved as expected and did not produce significant quantities of IL-2.
Becauses bacterial SAgs can activate T cells through two distinct activation pathways, both of which converge upon the phosphorylation of ERK-1/2 (54), we also measured the phosphorylation of ERK-1/2 in the presence of the various mutants as a measure of SpeC-induced T cell signaling (Fig. 3⇑B). Consistent with the IL-2 activation experiments, the mutant proteins SpeCT36A, SpeCY50A, SpeCY76A, SpeCI77A, SpeCY85A, and SpeCY87A were impaired for the ability to activate ERK-1/2. In addition, SpeCT33A showed a reduced ERK-1/2 activation phenotype that was not seen with the IL-2 activation experiments. The remainder of the mutants showed little to no reductions in activity. The control mutants SpeCY15A and SpeCD203A, as well as the additional double mutant SpeCY87A/D203A, behaved as expected and did not activate ERK-1/2.
These data indicate that a discrete number of residues within the β-barrel domain of SpeC are important for the activation of Vβ2.1+ T cells, and that these mutations likely disrupt the ability of SpeC to engage MHCα.
SpeC interacts with HLA-DR and HLA-DQ in different ways
To evaluate the ability of specific MHC II molecules to present the various SpeC mutants, we used BLS B cells transfected with specific MHC II alleles (HLA-DR1, HLA-DR4, or HLA-DQ2α3β) (42). BLS is an autosomal recessive disease in which the transcription factors that bind to MHC II promoters are mutated. As such, constitutive and inducible expression of MHC II is absent (55). Because SpeC was previously reported to activate T cells more strongly in the presence of HLA-DR4 compared with HLA-DQ2α3β (42), we first tested the activation of eJRT3-2.1 T cells with titrated SpeC in the presence of the different APC cell lines. As shown in Fig. 4⇓A, SpeC activated eJRT3-2.1 T cells at ∼100–1000 times lower concentration with BLS cells expressing HLA-DR4 compared with HLA-DQ2α3β. Thus, we conducted the remainder of experiments with the SpeC proteins at 1 ng/ml in the presence of HLA-DR4 or HLA-DR1 and at 100 ng/ml in the presence of HLA-DQ2α3β. The overall activation profile of the various SpeC mutants in the presence of HLA-DR4 (Fig. 4⇓B) or HLA-DR1 (Fig. 4⇓C), was very similar, with mutations at positions Tyr50, Tyr76, Ile77, Tyr85, Tyr87, and Asp183 showing the most drastic phenotypes. Mutations at positions Thr36 demonstrated an intermediate phenotype for both HLA-DR1 and HLA-DR4, Thr33 was significantly reduced for HLA-DR4, and Asn38 was significantly reduced for HLA-DR1. The remainder of the mutations at positions Thr34, His35, Tyr57, Glu58, and Lys189 showed little to no effect. The SpeCS80A mutant demonstrated a moderate but consistent increase in activity.
The activation profile of the various SpeC mutants in the presence of HLA-DQ2α3β (Fig. 4⇑D) showed an overall different pattern for the various mutations. Reductions in activity for mutations at SpeC positions Tyr50, Tyr76, and Tyr87 were common with all three MHC II molecules, whereas mutations at positions Thr36, Ile77, Tyr85, and Asp183 showed reduced activity only for the HLA-DR alleles and mutations at positions Thr34, His35, and Glu54 showed reduced activity only in the presence of HLA-DQ2α3β. In all cases, the control mutants SpeCY15A and SpeCD203A, as well as the additional double mutant SpeCY87A/D203A, behaved as expected and did not result in significant amounts of IL-2. Collectively, these results show that SpeC uses different patterns of residues to engage the α-chains of different MHC II molecules.
Three-dimensional model of the TCR-SpeC-(MHC II)2 signaling complex
A structural “map” of the various residues that were mutated in this study is summarized in Table I⇓ and shown as a ribbon diagram in Fig. 5⇓A, where the side chains of relevant amino acids, including the control mutations at SpeC positions Tyr15 and Asp203, are shown and indicated. In Fig. 5⇓, B and C, the molecular surfaces of SpeC that were important for the engagement of HLA-DR4 and HLA-DQ2α3β, respectively, are shown. Mutated positions that produced activation profiles similar to negative control conditions and were therefore determined to be critical, are colored red. Mutated positions with an intermediate phenotype are colored yellow, and those that did not result in significantly decreased activity are colored green.
In the absence of crystallographic information, the precise intermolecular contacts between the β-barrel domain of SpeC and the α-chain of MHC II are unknown. Therefore, we generated a three-dimensional model of how SpeC would potentially engage MHCα (Fig. 5⇑D). Despite low sequence identity, the N-terminal domain of SpeC is structurally more similar to TSST-1 (47) than to the group II and III SAgs; however, superposition of the SpeC-Vβ2.1 complex (13) onto the TSST-1-HLA-DR1 complex (3) generates major steric clashes between the CDR 3 loops of both TCRα and TCRβ with the MHC β1 domain and, thus, a similar orientation of SpeC and TSST-1 with MHC II is unlikely. Superposition of SpeC-Vβ2.1 complex onto the SEC3-HLA-DR1 complex, with minor alterations, produced a model with a number of features that explain our mutagenesis data. SpeC (in complex with Vβ2.1) was first superimposed onto the crystal structures of SEC3 in complex with HLA-DR1 (4). Because the molecular surface of SpeC important for engaging MHCα is significantly different from those of SAgs with structurally characterized MHCα interactions (discussed below), the complex was further manually docked based on our mutagenesis and functional data. Finally, the high-affinity, zinc-dependent MHC II interaction (6) and a human TCR α-chain (53) were superimposed onto the SpeC-Vβ2.1 complex. In this model, only minor steric clashes were found to occur between the TCR α-chain CDR2 and the MHC II β-chain (Fig. 5⇑D).
Fig. 5⇑E shows a ribbon diagram of residues from Ile8 to Asn78 of the α-1 domain of HLA-DR1 (DRA*0101). Side chains of DRA*0101 that make known intermolecular contacts with SEA, SEB, or SEC3 (2, 4, 8) are shown and labeled. Conserved side chains are colored gray, and side chains that differ between DRA*0101 and DQA1*0501 are colored magenta and orange, respectively. By combining our functional data (Fig. 5⇑B) and the proposed model (Fig. 5⇑D), the critical mutations in SpeC important for the engagement of HLA-DR4 form a near continuous surface predicted to make contacts within the first α-helix (MHCα residues αAsp55 to αAla68) and αLys39 of MHCα, whereas the intermediate SpeC mutations likely form contacts with the loop between the β1 and β2 strands near the MHCα residue αGln18 (Fig. 5⇑E).
Our model also predicts that the majority of residues important for the engagement of HLA-DQ2α3β form a thin but continuous surface, starting at SpeC Tyr76 and ending at Thr34 (Figs. 5⇑, A and C). The one critical residue from the HLA-DQ2α3β analysis, Tyr87, which is also critical for engaging the HLA-DR isoforms, likely hydrogen bonds with the side chain from the invariant MHCα residue Lys39. Our model also predicts that the lower portions of the SpeC-HLA-DQ2α3β interface would fit in a pocked formed between the MHCα β1-β2 and β3-β4 loops, potentially interacting with αPro18/αSer19 and αLeu36/αGly37/αArg38 (Fig. 5⇑E).
Bacterial SAgs represent a unique class of microbial toxins that have evolved to target the TCR and MHC II. The collective family of bacterial SAgs now vastly exceeds those that have been characterized with their TCR and MHC ligands on a structural level, and although there exists a high degree of structural homology between these SAgs, dramatically distinct molecular architectures of the SAg-mediated T cell signaling complexes can be formed (25).
In terms of MHCα engagement by bacterial SAgs, nearly all of the structural and functional analyses have been conducted with SAgs belonging to the group I (TSST-1), group II (SEB, SEC3, SpeA, and SSA (streptococcal superantigen)), and group III (SEA and SED) evolutionary lineages (2, 3, 4, 28, 30, 31, 56, 57, 58). In each case, the SAg N-terminal β-barrel domain is responsible for binding MHCα in a relatively low-affinity manner. Of these SAgs, TSST-1 represents an outlier where it binds predominantly to the MHC α-subunit, but it also extends over the antigenic peptide and makes contacts with the MHC β-subunit (3). Of the group II (SEB and SEC3) and III (SEA) SAgs that have been structurally characterized in complex with MHCα, each have similar “footprints” on MHCα, although SEA is rotated slightly away from HLA-DR1, presenting a smaller contact surface (8) with a reduced affinity (31, 59). Not surprisingly, the molecular surfaces of the β-barrel domains in group II and group III SAgs, which also includes SpeA and SSA (60, 61), are generally similar.
MHC II α-chains are much more conserved than β-chains, and HLA-DR α-chains are conserved to one known isoform (DRA*0101). Thus, in our experiments using HLA-DR1 and HLA-DR4, the α-chain is constant. Although the crystal structure of SpeC in complex with MHCα has not been solved, SpeC has been crystallized through the high-affinity MHCβ interaction with HLA-DR2a (DRA*0101/DRB5*0101) (6). In this case, the SpeCH35A mutant was used because the wild-type SpeC did not crystallize with HLA-DR2a, implying that an alternative interface was located at this site. Of the residues from DRB5*0101 that contact SpeC, each are conserved between DRB1*0101 and DRB1*0401 with one notable difference (DRB5*0101 Asp71 is a Gln in both DRB1 isoforms) (6). Thus, the contacts between SpeC and MHCβ from HLA-DR1 and HLA-DR4 are assumed to be identical. However, we did see a roughly 2-fold difference in potency exhibited by the BLS lines expressing HLA-DR4 or HLA-DR1 (Fig. 4⇑, B and C). These differences could be explained, in part, by the different peptides displayed in these MHC II molecules (27), as the peptide binding pockets are not identical. These variations could also be explained by potential differences in MHC II expression between transfectants, although no apparent difference in median fluorescence intensity was observed by flow cytometry when these cells were stained for HLA-DR expression (data not shown). Experiments conducted with HLA-DQ2α3β, as expected (42), were functionally much less efficient than those conducted with either HLA-DR molecule (Fig. 4⇑A). Again from the SpeC-HLA-DR2a complex, most of the residues predicted to engage DRB1*0101 and DRB1*0401 are conserved in DQB1*0302, including all those that form hydrogen bonds with SpeC (βThr21, βAsp76, βThr77, βArg80, and βHis81) (6). One exception includes position βGly84 in DRB1*0101 and DRB1*0401 (βGln84 in DQB1*0302), which forms van der Waals contacts. Based on the model in Fig. 5⇑D, the predicted SpeC “footprint” on MHCα contains a number of altered residues. These are illustrated in Fig. 5⇑E, where conserved MHCα side-chains are colored gray, DRA*0101-specific residues are colored magenta, and DQA1*0501-specific residues are colored orange. Thus, within our experimental system for the functional interaction of SpeC with the different MHC II isoforms, minor differences in MHCβ-chain residues, or different antigenic peptides (27), may potentially influence the activation experiments. However, due to the large number of altered residues between DRA*0101 and DQA1*0501 (Fig. 5⇑E), we believe that the major functional differences observed are most likely due to different α-chain contacts.
When comparing SpeC on a structural level with other SAgs, one strikingly common feature within the β-barrel domain of group II, group III, and group IV SAgs is the “polar pocket” region, corresponding to SpeC residues Glu54, Tyr76, and Tyr87. In group II and group III SAgs, this region engages the invariant αLys39 residue. SpeC Tyr87 was of critical importance in all of our functional assays, including the engagement of both HLA-DR and HLA-DQ isoforms. The SpeCY76A mutation, however, was critical for interaction with HLA-DR but showed an intermediate phenotype for HLA-DQ2α3β, whereas SpeCE54A did not produce a phenotype for either HLA-DR molecule but showed an intermediate phenotype for HLA-DQ2α3β. Taken together, the mutagenesis data within this region indicate that SpeC residues Tyr76 and Tyr87 likely form hydrogen bonds with the αLys39 side chain, analogous with SEC3. The observation that SpeCE54A did not produce a more drastic phenotype was surprising in that the equivalent residues SEA Asp70, SEB Glu67 and SEC3 Glu67 each form a key salt bridge with αLys39. This indicates that SpeC Glu54 does not form an equivalent salt bridge with αLys39. Although conserved as either an Asp or Glu in most group IV SAgs, the group IV SAg Streptococcus dysgalactiae-derived mitogen contains an Asn at this position, a residue predicted to disable a salt bridge with αLys39 (62). Thus, this residue may be largely dispensable for group IV SAg function, at least for engagement with HLA-DR. Comparing the HLA-SEA and HLA-SEC3 complexes, SEA binding to MHCα is rotated slightly away relative to SEC3. This rotation allows for the salt bridge between SEA Asp70 and αLys39, but SEA Tyr92 and SEA Tyr108 (corresponding to SpeC Tyr76 and SpeC Tyr87) are displaced away and are too far to form hydrogen bonds with αLys39 (8). Our data predict the reverse scenario with SpeC, where this SAg binds more distal to the antigenic peptide in HLA-DR, precluding the salt bridge and explaining why Glu54 is not critical. With HLA-DQ2α3β, SpeC residues Glu54, Tyr76, and Tyr87 were all important, indicating that with this isoform SpeC likely engages in a slightly “higher” position more analogous with SEC3.
Aside from the polar pocket region, the remaining surface of the SpeC β-barrel predicted to engage MHCα is drastically different compared with group II and group III SAgs. A flexible loop region found in the SEs termed the “cysteine loop,” which is located between the β4 and β5 strands (residues Cys93 to Cys110 in SEC3), is unique to group II and group III SAgs. This region corresponds to SpeC residues Asn79 through Gly83. In group II and group III SAgs, the proximal region of the loop extends away from the SAg surface making a number of contacts with MHCα (e.g., SEC3 residues Asn92, Tyr94, and Ser96) (4). In SpeC, the β4-β5 region is much shorter, and this results in a concave surface on SpeC where the majority of the residues critical for engagement of HLA-DR map (SpeC residues Tyr50, Tyr76, Ile77, and Tyr85) (Fig. 5⇑B). Our model predicts that the α-helix from the MHC α-1 domain would fit into this groove (Fig. 5⇑D), thus explaining this functional “hot spot”. Within this region, SpeCY50A resulted in a critical phenotype when presented by LG-2 cells or cells expressing either HLA-DR1 or HLA-DR4. However, an intermediate phenotype was shown for the HLA-DQ2α3β cell line. SpeCI77A and SpeCY85A produced a similar phenotype, although reduced activity did not reach statistical significance for the HLA-DQ2α3β cell line. Based on our model, these three residues likely engage the α1 domain, near to positions αAla61 and αAla68 found in DRA*0101 (Fig. 5⇑E). These two residues are αThr61 and αHis68 in DQA1*0501 (Fig. 5⇑E), which may partially occlude insertion of the α1 domain onto the surface of SpeC, and this is consistent with the polar pocket mutations where the SpeC β4-β5 loop would be pushed laterally, forcing SpeC to bind “higher” on the HLA-DQ2α3β surface. This isoform variation in MHCα may represent a key mechanism that results in allelic discrimination between HLA-DQ alleles, from HLA-DR, at least for SpeC. One of the most dramatic differences between the HLA-DR and HLA-DQ isoforms resulted from the mutation at SpeC Asp183. The mutation appears to be an outlier from the other mutations and may require a water molecule to bridge the intermolecular contacts with MHCα. The most likely contact in DRA*0101 would be αGlu55, because DQA1*0501 contains a shorter side chain Asp55 that may prevent intermolecular contacts (Fig. 5⇑E). Lastly, for both HLA-DR isoforms SpeCS80A consistently produced a mildly but significantly increased activation phenotype compared with wild-type SpeC. The reason for this is unknown, but from the Vβ2.1-SpeC crystal structure SpeC Asn79 formed hydrogen bonds with the main chain of the Vβ2.1 CDR3 loop, and the SpeCS80A mutant may alter these contacts. This would be consistent with HLA-DQ2α3β, where this region of the loop would be more distal to the Vβ CDR3 loop, and the SpeCS80A mutant did not show an increase in activity.
The other notable difference between group II, group III, and group IV SAgs within the β-barrel domain is a loop located between the β1–β2 sheets in SEs termed the “hydrophobic ridge”. Compared with SpeC, this ridge is extended by one additional amino acid in SEA, SEB, and SEC3. This results in an altered orientation, such that there are no similarly positioned residues for SpeC residues Phe31, Ser32, and Thr33. However, within the group IV subclass, this loop is structurally conserved (e.g., SpeC, SpeG, SpeJ, and SMEZ (streptococcal mitogenic exotoxin Z)). This region in SEC3 in functionally important because a series of hydrophobic loop variants, generated by random mutagenesis coupled with phage display to select for affinity matured variants, resulted in variants with nearly 60-fold stronger binding affinities for HLA-DR1 (4). Within this region in SpeC, mutations important for engagement with HLA-DR4 that were not important for engagement with HLA-DQ2α3β were at SpeC positions Thr33and Thr36. Thr33 could potentially interact directly with αGln18 (Fig. 5⇑E), whereas Thr36 forms a concave surface on the SpeC molecular surface (Fig. 5⇑B). It is difficult to envision from the model any direct interactions between Thr36and MHCα. The Oγ1 atom on Thr36 forms a hydrogen bond with Thr33 Oγ1, and this interaction may be important for the orientation of Thr33 to make productive contacts with αGln18. This would be consistent with the HLA-DQ2α3β interaction, where neither mutation produced a phenotype. Mutation at this position produced an intermediate phenotype for HLA-DR4, but not for HLA-DR1 or HLA-DQ2α3β. The opposite phenotype was seen for the SpeC Asn38 mutation, where there was no difference for activation by HLA-DR4 while there was a minor defect for HLA-DR1. The reasons for these minor differences are not readily apparent, as the α-chains for HLA-DR1 and HLA-DR4 are identical. It is formally possible that β-chain polymorphisms influence the α-chain conformation within this region or that altered peptide-SAg interactions between the two HLA-DR isoforms indirectly influence the α-chain-SpeC interaction. Thr34 is not a conserved residue among SAgs characterized to engage MHCα, and the SpeCT34A mutation displayed only a minor reduction in activation for HLA-DQ2α3β. SpeC His35 however, represents a highly conserved residue that is also found at this position in SSA, SpeA, SEA, and SEC3 (in SEB it is Phe47). Our data indicate that despite the conservation of this residue in other SAgs, with SpeC it played no role for the engagement of HLA-DR isoforms but did show an intermediate phenotype with HLA-DQ. The most likely explanation for this is that αGly37 present in HLA-DQ alleles (αAla37 in DRA*0101) (Fig. 5⇑E) allows for a more flexible loop in this region that could accommodate DQA1*0501 main chain interactions with the SpeC His35 side chain.
SpeC belongs to the SAg group IV, an evolutionary branch that contains only streptococcal SAgs, and group IV SAgs have been poorly characterized with respect to MHCα engagement. Our data have revealed a functional epitope within the SpeC β-barrel domain that is critical for engagement of HLA-DR and indicates that SpeC, similarly as group I, group II, and group III Sags, possesses a low-affinity MHC II binding interface that is required for the activation of T cells. Our data also predict that polymorphisms within the α-1 domain of MHCα may be primarily responsible for the weak activity associated with SpeC when presented by HLA-DQ isoforms and that in such cases SpeC likely engages in an inefficient and slightly altered orientation. Although the β-barrel domain of group IV SAgs is considerably different from those of group II and group III SAgs, our functional experiments indicate that the polar pocket region, which is conserved in group II, group III, and group IV SAgs, may represent a new rational target for broad spectrum inhibitors of bacterial SAgs.
The authors have no financial conflict of interest.
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↵1 This work was supported by Canadian Institutes of Health Research (CIHR) operating grants to J.K.M. and J.M. and National Institutes of Health Grant AI55882 to E.J.S. Stipend support to K.K. and A.K.M.N.R. was provided in part by scholarships from the Schulich School of Medicine and Dentistry and by an Early Research Award from The Ontario Ministry of Research and Innovation. Laboratory infrastructure was supported by a New Opportunities Fund award from the Canadian Foundation for Innovation and the Ontario Innovation Trust (to J.K.M). J.M. holds a Tier I Canada Research Chair in Immunobiology, and J.K.M. holds a New Investigator award from CIHR.
↵2 Address correspondence and reprint requests to Dr. John K. McCormick, Department of Microbiology and Immunology, University of Western Ontario, London, Ontario, Canada N6A 5C1. E-mail address:
↵3 Abbreviations used in this paper: SAg, superantigen; BLS, bare lymphocyte syndrome; MHCα, MHC II α-chain; MHCβ, MHC II β-chain; SE, staphylococcal enterotoxin; SEA/SEB/SEC3/SEE, staphylococcal exotoxin A, B, C3, or E; SpeA/SpeC, streptococcal pyrogenic exotoxin A or C; SSA, streptococcal superantigen; TEV, tobacco etch virus; TSST-1, toxic shock syndrome toxin-1; Vβ, variable region of the TCR β-chain.
- Received May 2, 2008.
- Accepted June 26, 2008.
- Copyright © 2008 by The American Association of Immunologists