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Chlamydiae sp. are obligate intracellular pathogens that cause a variety of diseases in humans. Adhesion of the infectious elementary body to the eukaryotic host cell is a pivotal step in chlamydial pathogenesis. Here we describe the characterization of members of the polymorphic membrane protein family (Pmp), the largest protein family (with up to 21 members) unique to Chlamydiaceae. We show that yeast cells displaying Pmp6, Pmp20 or Pmp21 on their surfaces, or beads coated with the recombinant proteins, adhere to human epithelial cells. A hallmark of the Pmp protein family is the presence of multiple repeats of the tetrapeptide motifs FxxN and GGA(I, L, V) and deletion analysis shows that at least two copies of these motifs are needed for adhesion. Importantly, pre-treatment of human cells with recombinant Pmp6, Pmp20 or Pmp21 protein reduces infectivity upon subsequent challenge with Chlamydia pneumoniae and correlates with diminished attachment of Chlamydiae to target cells. Antibodies specific for Pmp21 can neutralize infection in vitro. Finally, a combination of two different Pmp proteins in infection blockage experiments shows additive effects, possibly suggesting similar functions. Our findings imply that Pmp6, Pmp20 and Pmp21 act as adhesins, are vital during infection and thus represent promising vaccine candidates.
Chlamydiae are Gram-negative bacteria with compact genomes, and some species represent significant threats to human health. Chlamydia trachomatis is the most prevalent sexually transmitted bacterial pathogen worldwide (Schachter, 1999). Chlamydia pneumoniae is an important respiratory pathogen, causing pneumonia and bronchitis, and is associated with several chronic diseases (Schachter, 1999). Despite the clinical relevance of Chlamydia, no vaccine is available for use in humans (Brunham and Rey-Ladino, 2005; Puolakkainen, 2009). Chlamydia species have a unique biphasic developmental cycle, alternating between the infectious elementary body (EB) and the metabolically active, intracellular reticulate body (RB) that replicates in eukaryotic cells (for reviews see Moulder, 1991; Hatch, 1999). The mechanisms underlying EB infectivity are unclear (Campbell and Kuo, 2006; Scidmore, 2006).
Polymorphic membrane proteins (Pmps) found in species of the Chlamydiaceae are candidate adhesins (Longbottom et al., 1998; Stephens et al., 1998; Grimwood and Stephens, 1999; Kalman et al., 1999; Knudsen et al., 1999; Read et al., 2003; Wehrl et al., 2004; Crane et al., 2006). The C. trachomatis pmp gene family has nine members (Stephens et al., 1998; Grimwood and Stephens, 1999; Tan et al., 2006), representing six subtypes: A, B/C, D, E, G and H. C. pneumoniae has 21 pmp genes, 13 of which (pmp1–pmp13) belong to subtype G (Grimwood and Stephens, 1999; Kalman et al., 1999). The pmp genes make up more than 5% of the total coding capacity of the genome, and are unique to the Chlamydiaceae, suggesting that their products might be virulence factors (Horn et al., 2004). The various Pmp families show little similarity in amino acid sequence, but all members contain multiple repeats of the motifs GGA(I, L, V) and FxxN (Grimwood and Stephens, 1999; Rockey et al., 2000). The GGAI sequence is predicted to be present in only 10 other proteins (and only in one copy per protein) in the chlamydial proteomes, underscoring the over-representation of the motif in the Pmp families (Grimwood and Stephens, 1999). Similarly, the FxxN motif is found on average 13.6 times per Pmp protein in C. trachomatis and 11.3 times in C. pneumoniae, respectively, while its average incidence in the rest of the proteome is 0.73 (C. trachomatis) or 0.84 (C. pneumoniae) (Grimwood and Stephens, 1999).
Pmp proteins resemble classical autotransporters (ATs), with (i) an N-terminal sequence for sec-dependent translocation across of the cytoplasmic membrane, (ii) a C-terminal β-barrel domain with a phenylalanine at the end suggestive for a outer membrane localization of Pmp proteins, and (iii) a central passenger domain (PD) responsible for the protein's function that can remain surface-localized or be secreted (e.g. Pmp21 in Fig. 1A) (Henderson and Lam, 2001; Dautin and Bernstein, 2007; Wells et al., 2007). The Pmp PDs, which carry nearly exclusively the tetrapeptide repeats, probably adopt a parallel β-helix structure (Vandahl et al., 2002). Like other AT proteins, Pmps apparently undergo proteolytic processing (e.g. Pmp21 in Fig. 1B) (Vandahl et al., 2001; 2002; Vretou et al., 2003; Wehrl et al., 2004; Kiselev et al., 2009; Swanson et al., 2009). However, there is no evidence for secretion of Pmps by the AT pathway.
Some Pmps are known to be surface-located on infectious EBs, and are thus positioned at the interface between pathogen and the infected cell (Vandahl et al., 2002; Wehrl et al., 2004; Crane et al., 2006; Kiselev et al., 2009; Swanson et al., 2009). Antibodies against Pmp21 from C. pneumoniae or PmpD from C. trachomatis inhibit infection in vitro (Wehrl et al., 2004; Crane et al., 2006). Patients infected with either species show significant serological responses to various Pmps (Bunk et al., 2008; Tan et al., 2009). The high degree of variation found among pmp gene families suggests that they are under selective pressure (Grimwood and Stephens, 1999; Shirai et al., 2000; Pedersen et al., 2001; Rocha et al., 2002; Gomes et al., 2005; 2006; Tan et al., 2009). Indeed, C. trachomatis inclusions formed in cultured cells exhibit variability in the sets of Pmps they express, suggesting they confer antigenic diversity (Tan et al., 2010).
We show that Pmp6, Pmp20 and Pmp21, representing three of the six subtypes (B/C, D, G), act as adhesins during infection by C. pneumoniae. FxxN and GGA(I, L, V) motifs are necessary for this activity. Pmp21 has several adhesive domains, but the strongest cell-binding and infection-blocking activities are associated with processed forms of the protein known to occur in vivo. A 32-residue Pmp21 peptide including a FxxN/GGAV doublet can competitively reduce a C. pneumoniae infection. Interestingly, a combination of two different Pmp proteins in infection blockage experiments shows additive effects, possibly suggesting similar functions.
Pmp21 and PmpD from C. trachomatis are targets of neutralizing antibodies and may function in pathogenesis (Wehrl et al., 2004; Crane et al., 2006). To ask if Pmp21 is an adhesin, we used a yeast display system (Fig. S1) (Moelleken and Hegemann, 2008). The PD of Pmp21 (residues 30–1144) (Fig. 1C) was fused to the yeast surface protein Aga2p (Aga2–Pmp21-PD) and the cells were tested for adhesion to human epithelial HEp-2 cells. Yeast cells displaying Aga2–Pmp21-PD, but not Aga2 alone or Aga2 fused to the chlamydial outer membrane protein OmpA (MOMP), adhered to HEp-2 cells (Fig. 1D; Fig. S2). Indeed, cells displaying Pmp21-PD showed significantly stronger adhesion to HEp-2 cells than did cells presenting Yersinia pseudotuberculosis invasin (Aga2–Inv197) or chlamydial OmcB (Fig. 1E) (Dersch and Isberg, 1999; Moelleken and Hegemann, 2008). Thus, Pmp21-PD can mediate adhesion to human cells.
To identify the parts of C. pneumoniae Pmp21 that mediate binding, we tested four subdomains of Pmp21-PD in the yeast system (Fig. 1C). Any one of them fused to Aga2 mediated adherence to HEp-2 cells, although all were less effective than Pmp21-PD (Fig. 1F).
We also performed latex bead assays with Pmp21 (Dersch and Isberg, 1999). We purified Pmp21-PD and the four Pmp21 domains A–D, expressed as His-tagged proteins in Escherichia coli, and incubated them with latex beads. The coated beads were then tested for adhesion to HEp-2 cells. Beads loaded with recombinant MBP or MBP-OmpA or BSA exhibited scarcely any binding to HEp-2 cells, while beads bearing His- or MBP-tagged invasin or Pmp21-PD (or any of its four fragments) clearly bound to human cells (Fig. 1G; Fig. S2). Thus, Pmp21-PD has several independent binding domains that mediate adherence to human cells. Published work suggests that Pmp21 is cleaved in vivo, and infectious EBs probably carry at least three different processed forms (N-Pmp21, M-Pmp21 and C-Pmp21) (Fig. 1B). The last, comprising the β-barrel unit, probably remains in the outer membrane (Grimwood et al., 2001; Vandahl et al., 2002; Wehrl et al., 2004). We created two variants, Pmp21-E and Pmp21-G, corresponding to N-Pmp21 and M-Pmp21 respectively (Fig. 1C). Latex beads coated with either adhered to HEp-2 cells just as well as the other Pmp21 variants tested (Fig. 1G). Thus, the processed N-Pmp21 and M-Pmp21 forms found on EBs can bind to human cells.
The only feature common to the variants tested so far is the presence of repeated GGA(I, L, V) and FxxN motifs (Fig. 1C). We selected Pmp21-B and Pmp21-D, which showed comparable adhesion properties in the yeast assay, but have very different numbers of tetrapeptide repeats (Fig. 2), for further study. Deletion experiments revealed that the 50-residue Pmp21-BΔ2, with one FxxN and two GGA(I, V, L) repeats, behaved like Pmp21-B. In contrast, N-terminal truncation of Pmp21-D, deleting the only two tetrapeptide FxxN motifs present, resulted in a significant reduction (Pmp21-DΔ1) or complete loss (Pmp21-DΔ2) of adhesiveness (Fig. 2). Thus Pmp21 domains with two FxxN motifs (Pmp21-D) and one FxxN and two GGA(I, V, L) motifs (Pmp21-BΔ2) both show significant adhesion to HEp-2 cells.
To confirm that these motifs are necessary for Pmp21-mediated adhesion to human cells, we chose Pmp21-A and Pmp21-D (Fig. 3A). We mutated the FYKN motif in Pmp21-A to SYKV, leaving the GGAV motif unchanged. Beads bearing Pmp21-A-mut1 exhibited no adhesion to human cells. Similarly, deletion of the GGAV motif in Pmp21-A, leaving the FYKN motif intact, abrogated adhesion (Pmp21-A-mut2, Fig. 3A and B). In Pmp21-D we changed a single residue in the N-terminal FYGN motif, keeping the FEGN motif intact, or changed both motifs. All three mutant forms of Pmp21-D showed no adhesive capacity (Fig. 3A and C). Hence the FxxN and GGAV motifs are necessary for binding of the Pmp21A and Pmp21D domains to HEp-2 cells. A minimum of two copies of either motif (FxxN + GGAV or FxxN + FxxN) is required for adhesion.
Thus far our data indicate that Pmp21-PD on yeast cells or latex beads can bind human cells. Next we analysed the localization of Pmp21 on infectious EBs. Anti-Pmp21-D antibody specifically detects a 55–60 kDa protein in lysates of HEp-2 cells infected with C. pneumoniae prepared 36–96 h post infection (p.i.). This probably corresponds to the processed M-Pmp21 identified previously in RBs (Fig. 4A) (Wehrl et al., 2004). The high levels found at 96 h p.i. suggested that this form might be present in EBs and, indeed, a strong M-Pmp21 signal was observed in extracts of EBs (Fig. 4B). In EB extracts containing Sarkosyl and DTT, additional weak bands were detected: one of > 170 kDa corresponding to the full-length N/M/C-Pmp21 and one of > 130 kDa – probably N/M-Pmp21 (Fig. 4B). This pattern has been described for Pmp21 isolated 4 days p.i. (Wehrl et al., 2004).
Indirect immunofluorescence microscopy of infected cells revealed that Pmp21 can be detected in the chlamydial inclusion and colocalizes with the bacteria at all times analysed. As the C. pneumoniae inclusions are completely filled with bacteria we could not inspect the inclusion lumen for possible Pmp21 signals not associated with bacteria. This had been reported for the C. trachomatis homologue PmpD (Kiselev et al., 2009; Swanson et al., 2009). The Pmp21 staining pattern did not change significantly over the course of the infection. Pmp21 was never found outside the inclusion (Fig. S3A). Next we analysed the localization of Pmp21 in greater detail. HEp-2 cells infected with C. pneumoniae were fixed with methanol or formaldehyde 48 h p.i., and incubated with the anti-Pmp21-E and an antibody against either the intrachlamydial DnaK or the extrachlamydial OmpA. In methanol-fixed cells, all antibodies reacted with the bacteria in the inclusion. Anti-OmpA antibody, which stains the chlamydial surface, colocalized with anti-Pmp21, giving a ring-like signal (Fig. 4D). In formaldehyde-fixed cells intracytoplasmic proteins are inaccessible to antibodies (the anti-DnaK antibody gave only a very weak signal), while both the anti-OmpA and anti-Pmp21 antibodies reacted, indicating that their targets are located on the bacterial surface (Fig. 4C, PFA; Fig. S3C). At higher magnification in formaldehyde-fixed cells, a dotted ring-like pattern surrounding the DAPI signals representing the bacteria was generated by the anti-Pmp21 antibodies (Fig. 4E; white arrows mark single Pmp21 signals). Microimmunofluorescence of viable, unfixed C. pneumoniae EBs confirmed that OmpA and Pmp21 were localized on the bacterial cell surface, while DnaK was only rarely accessible (Fig. S3B).
We then tested directly whether Pmp21 on the EB surface is needed for chlamydial attachment to host cells. Incubation of purified EBs with anti-Pmp21 reduced infectivity of C. pneumoniae by up to 80%; while incubation with pre-immune serum only reduced infection by 35% (Fig. 5A). We then blocked Pmp21 binding sites on human cells by pre-incubation of HEp-2 cells with Pmp21-PD and again found strong (~90%) inhibition of infection by C. pneumoniae EBs (Fig. 5B). Pre-incubation with the individual Pmp21 domains shown to bind to HEp-2 cells also reduced infection rates. Pmp21-E and Pmp21-G, which resemble the naturally occurring processed forms N-Pmp21 and M-Pmp21 (see Fig. 1B and C), inhibited subsequent infection by ~40% (Fig. 5B). Furthermore, binding of infectious EBs stained with the fluorescent dye CFSE to HEp-2 cells was dose-dependently reduced by up to 90% following pre-incubation with Pmp21-PD (Fig. 5C). Taken together, these results demonstrate that EB-associated Pmp21 mediates adhesion of EBs to human cells and is involved in the infection process.
Finally, we asked if a peptide containing a typical tetrapeptide motif doublet derived from Pmp21 could block EB binding and reduce infectivity. We chose the sequence between positions 745 and 776 in M-Pmp21, which has an N-terminal FSDN and a C-terminal GGAI motif. Pre-incubation of HEp-2 cells with the synthetic peptide inhibited infection by C. pneumoniae by up to 40%, while a scrambled peptide had no effect (Fig. 5D). This result underlines the importance of the tetrapeptide motifs for Pmp21 function in C. pneumoniae infections.
Pmp21 is one of 21 Pmps in C. pneumoniae. To ask whether other subtypes are relevant for C. pneumoniae infections, we chose Pmp6 (subtype B/C) and Pmp20 (G), which resemble Pmp21 (D) in length and in possessing > 30 tetrapeptide motifs in their N-terminal and central regions (Fig. 6A). Fluorescent beads coated with rPmp6-1 or rPmp20-1 adhered more strongly to epithelial cells than beads coated with rPmp21-E or invasin (Fig. 6B). Consistent with this, binding of viable, fluorescently labelled infectious EBs to HEp-2 cells was significantly reduced when the human cells were pre-incubated with 200 µg ml−1 rPmp6-1 or rPmp20-1 (Fig. 6C). Recombinant Pmp21-E had a similar effect, confirming the result obtained for the Pmp21 full-length passenger domain Pmp21-PD (see Fig. 5C). Thus, our findings imply that Pmp6, Pmp20 and Pmp21 all contribute to adhesion of C. pneumoniae EBs to target cells.
Thus far the results obtained for rPmp6 and rPmp20 parallel those obtained for Pmp21. We therefore tested whether Pmp6 or Pmp20 are also relevant for the chlamydial infection. Pre-incubation of HEp-2 cells with recombinant Pmp6 or Pmp20 inhibited subsequent infection by the bacteria in a dose-dependent manner (Fig. 7A). The kinetics of Pmp20- and Pmp21-induced inhibition of infection are very similar, but differ from the results for Pmp6. Nevertheless, these data show that Pmp6 and Pmp20 contribute to EB adhesion and to subsequent C. pneumoniae infection.
The data obtained for the three Pmp proteins suggest that the proteins might have overlapping functions. We therefore combined two different Pmp proteins in a single infection blockage experiment. Human cells were pre-incubated with either rPmp6-1 or rPmp21-E protein alone, or a combination of both. Pre-treatment of human cells with 25 µg ml−1 rPmp6-1 or rPmp21-E did not reduce infection (106% and 103% of the control values respectively). Interestingly, the combination of 25 µg ml−1 rPmp21-E and 25 µg ml−1 rPmp6-1 significantly reduced subsequent infection to 87% (P-value: 0.001), and 50 µg ml−1 rPmp21-E reduced it further (80%), while 50 µg ml−1 rPmp6-1 had no effect (102%). These data suggest that soluble rPmp6-1 and rPmp21-E additively inhibit infection, suggesting some overlap in the functions of the native proteins during a chlamydial infection.
Successful infection of host cells depends on a battery of virulence factors, including specialized bacterial surface structures which mediate uptake by host cells (Carbonnelle et al., 2009; Kline et al., 2009). Chlamydiae enter cells via multiple routes, using poorly understood mechanisms (Campbell and Kuo, 2006). In this study we show that Pmp6, Pmp20 and Pmp21 act as adhesins during infection of human cells by C. pneumoniae.
Pmps exhibit characteristic features of autotransporters, including proteolytic processing (Grimwood and Stephens, 1999; Henderson and Lam, 2001). Pmp21, like its C. trachomatis homologue PmpD, is processed during infection, and processed forms of Pmp6 and Pmp20 have been identified in purified EBs (Vandahl et al., 2002; Wehrl et al., 2004; Kiselev et al., 2009; Swanson et al., 2009). Full-length Pmp21 (N/M/C-Pmp21), the intermediate N/M-Pmp21 and the fully processed N-Pmp21 were detected during infection and in infectious EBs, while proteome studies of EBs identified the putative end-products of processing, N-Pmp21, M-Pmp21 and the translocator unit C-Pmp21 (Fig. 1B) (Vandahl et al., 2002; Wehrl et al., 2004). Using antibodies against the C-terminal part of the PD we detected a protein corresponding in size to the fully processed M-Pmp21 both during infection of HEp-2 cells and on EBs (Fig. 4). Indeed, it appears that the majority of Pmp21 is fully processed during infection, resulting in N-Pmp21 (Wehrl et al., 2004), M-Pmp21 (this work) and presumably C-Pmp21 as well. N- and M-Pmp21 remain associated with the bacterial cell surface throughout infection (Fig. 4; Fig. S3) (Wehrl et al., 2004). This differs from the more complex set of processed forms described for the homologous PmpD protein from C. trachomatis (Kiselev et al., 2009; Swanson et al., 2009).
Our data show that M-Pmp21 colocalizes with the outer membrane protein OmpA (MOMP), confirming other Pmp21 localization studies (Vandahl et al., 2002; Wehrl et al., 2004). Interestingly, our anti-Pmp21-E antibody detected dotted, ring-like structures associated with the bacterial cell surface (Fig. 4E). It remains to be seen whether these dots correspond to the oligomeric structures observed for PmpD (Swanson et al., 2009). Pmp6 and Pmp20 are also found associated with the bacterial cell surface (Montigiani et al., 2002; Vandahl et al., 2002). As with Pmp21, the adhesive and infection-relevant properties of Pmp6 and Pmp20 described here were found to reside in their N-terminal segments.
Our studies show that Pmp21-PD (essentially equivalent to N/M-Pmp21), Pmp21-G and Pmp21-E (similar to N- and M-Pmp21 respectively) retain adhesive capacities for HEp-2 cells similar to those found for Pmp21-PD. Interestingly, even small domains of only 50 amino acids (e.g. Pmp21-BΔ2) display undiminished adhesion. Curiously, the adhesive capacity of Pmp21-E and -G is not significantly enhanced relative to that of the smaller fragments. The presence of multiple binding sites on N-Pmp21 and M-Pmp21 could allow them to engage several receptor molecules, or several binding sites on a single receptor molecule simultaneously. We can exclude polymeric glycosaminoglycan structures on HEp-2 cells as potential Pmp21 receptors, as yeast cells presenting Pmp21-B or -D adhered equally well to GAG-deficient CHO lines and the control line K1 (data not shown). GAGs are required for binding of OmcB adhesin, however (Moelleken and Hegemann, 2008), although it is not clear how the activity of OmcB and the Pmp adhesins is co-ordinated during adhesion.
All Pmp21 domains tested showed significant adhesion to HEp-2 cells, while their ability to inhibit infection varied. Pmp21 variants resembling the natural processed forms were most effective, suggesting that these present optimal binding conformations to the receptor(s). This may also explain why the Pmp21-derived peptide had only moderate infection-blocking activity. The inhibitory effect of soluble recombinant Pmp21 protein was confirmed by the neutralizing activity of anti-Pmp21-E antibodies, in agreement with published data for N-Pmp21 and PmpD from C. trachomatis (Wehrl et al., 2004; Crane et al., 2006). Recombinant Pmp6 and rPmp20 also exhibited adhesion to epithelial cells, reduced binding of infectious EBs to HEp-2 cells, and blocked subsequent infection (Figs 6B and C and 7A). Unlike Pmp6, Pmp20 showed a dose dependence similar to Pmp21. This suggests that binding of human cells might vary with Pmp subtype.
All Pmps have multiple copies of the motifs FxxN and GGA(I, L, V) in their N-terminal segments (Grimwood and Stephens, 1999). We found that adhesion of all Pmp21 domains tested required a minimum of two copies of these motifs [2x FxxN or FxxN plus GGA(I, L, V)]. We did not test whether two copies of the GGA(I, L, V) motif are sufficient for adhesion. The distribution of these motifs in Pmps shows no obvious pattern, but the two types often occur as doublets of the form FxxN-x5–17-GGA(I, L, V). Indeed, a small M-Pmp21 fragment with a typical doublet (FxxN-x8-GGAI) exhibited adhesion and interfered with infection by C. pneumoniae (Fig. 5D). The motifs may be required for maintenance of the Pmp conformation that permits adhesion, or might directly mediate interaction with human receptors, or both. Alternatively, the wide variation in the number and spacing of the two motifs could provide a surface unique for each individual Pmp. Repeats of short sequences have been described for other adhesive autotransporters, but no function has been attributed to them (Girard and Mourez, 2006).
Our data show that Pmp6, Pmp20 and Pmp21, representing three of the six Pmp subtypes (G, B/C and D respectively), exhibit very similar functional properties (adhesion, partial inhibition of EB binding to human cells, blockage of subsequent infection). These observations suggest that they have similar or even overlapping functions. In agreement with this, we found that pre-incubation of HEp-2 cells with two different Pmp proteins (rPmp6-1 and rPmp21-E) in a single experiment significantly reduced infection, under conditions where each protein alone was ineffective (Fig. 7B). These preliminary data are concordant with a hypothetical model, in which Pmp6 and Pmp21 have similar but non-redundant roles during adhesion and invasion, possibly recognizing the same host cell receptor or a group of related receptors. We have preliminary data that Pmp20 also participates in this functional network (data not shown). Pmp6 belongs to subtype G, which comprises 13 members in C. pneumoniae (Grimwood and Stephens, 1999). Other Pmps of this subtype might have similar roles in infection, as at least nine are reported to be present on infectious EBs (Vandahl et al., 2001; Montigiani et al., 2002). Indeed, several, or perhaps all, expressed Pmps might together form a supramolecular complex that is required for efficient adhesion. Anti-Pmp21 does not cross-react with Pmp6 or Pmp20 in Western blots (data not shown); nevertheless, it effectively blocks adhesion of C. pneumoniae. If these three Pmps were involved in a multimeric complex on the bacterial cell surface, an antibody against anyone could conceivably block adhesion mediated by the others. Indeed, studies in C. trachomatis and C. psittaci suggest that Pmp PDs could perform homo- or hetero-oligomeric interactions with other Pmps (Tanzer et al., 2001; Swanson et al., 2009). Those interactions could be modulated by host cell enzymes, e.g. by protein disulphide isomerase (PDI), a surface-located host protein, which is necessary for EB entry (Abromaitis and Stephens, 2009).
The diversity of the Pmp superfamily may also be attributable to antigenic variation as in the case of the Opa protein family in Neisseria gonorrhoeae (Grimwood and Stephens, 1999; Carbonnelle et al., 2009). This could compromise the host's ability to mount a potent humoral immune response and thus disable host defence mechanisms. This idea is supported by the important finding that Pmp10 from C. pneumoniae, as well as all nine Pmps (including the Pmp21 homologue PmpD) in C. trachomatis, are variably expressed in inclusions formed in cultured cells (Pedersen et al., 2001; Tan et al., 2010). This may explain why sera from C. trachomatis-infected patients show significant differences in Pmp-specific antibody profiles (Tan et al., 2009). If the expression of Pmps on the EB surface also varies in C. pneumoniae, the pool of 21 Pmp proteins could form the basis for broad antigenic diversity, while ensuring that EB adhesion properties remain stable.
Pmp proteins may function in concert with other EB surface proteins. For example, the C. trachomatis PmpD seems to be in close contact with serovariable MOMP and LPS, as antibodies against either block neutralization by PmpD antibodies, suggesting a decoy-like immune evasion strategy (Crane et al., 2006). Likewise, in C. pneumoniae Pmp10 apparently protects the C-terminal part of MOMP from proteolytic cleavage (Juul et al., 2007). While for the C. trachomatis MOMP unspecific interactions with host cells have been proposed (Su et al., 1990), we could not detect adhesion of recombinant C. pneumoniae MOMP to HEp-2 cells, possibly due to lack of the post-translational modifications that have been found in native C. psittaci and C. trachomatis MOMPs (summarized in Campbell and Kuo, 2006).
Safe recombinant vaccines, based on a small number of antigenic proteins, are emerging as the most cost-effective way of combating infectious diseases. Adhesins are interesting vaccine candidates, as some provide protection against infection in animal models (Kline et al., 2009). A combination of Pmp proteins could yield a very effective vaccine, and would minimize problems associated with antigenic variation that may be linked with this class of proteins.
Escherichia coli strain XL-1 blue (Stratagene) was used for protein expression and plasmid amplification. C. pneumoniae GiD was propagated in HEp-2 cells (ATCC No. CCL-23) as described (Jantos et al., 1997). Chlamydial EBs were purified by using a 30% gastrographin gradient (Schering). The Saccharomyces cerevisiae strain yEG2 (MATa ura3-52 trp1 LEU2 his3Δ200 pep4:HIS3 prb1Δ.6R can1 GAL1p-AGA1::pIU211 leu2Δ1::pCM149) was used for yeast display experiments: the GAL1 promoter of the chromosomally integrated GAL1p-AGA1 expression unit in strain EBY100 (Invitrogen) was substituted for the KanMX-tetO7-CYC1p promoter by PCR-based homologous recombination using plasmid pAH3. Strain yEG2 was routinely grown in selective synthetic dextrose (SD) medium plus 2% glucose (Sherman, 1991).
Plasmids were generated in S. cerevisiae as described (Moelleken and Hegemann, 2008). The yeast expression vector pEG2 (this work) was generated by replacing the GAL1 promoter in pYD1 (Invitrogen) with the tetO7-CYC1 promoter amplified by PCR from pCM189 (Gari et al., 1997). The E. coli expression vector pKM32 (this work) was constructed by integration of a CEN6 ARS4 URA3 cassette into XbaI/PvuII-linearized pQE-31 (Qiagen). The pmp21 variants were amplified by PCR using C. pneumoniae GiD DNA as template, and cloned into NotI-digested pEG vector or fused N-terminally to a His6-Tag and cloned into the SmaI site in pKM32. Pmp6 or pmp20 variants and the Y. pseudotuberculosis sequence encoding the invasin fragments Inv197 (aa 772–969) and Inv497 (aa 490–969) subcloned from pRI285 (Dersch and Isberg, 1999) were cloned into pKM32 as described above. Plasmid pYD1-Inv197 has been described before (Moelleken and Hegemann, 2008). Site-specific mutagenesis was performed using oligonucleotides. All constructs were sequenced prior to use.
For expression of Aga2p or Aga2p fusion proteins in yEG2, cells were grown in selective SD medium and harvested in logarithmic phase. Expression and purification of His6-tagged fusion proteins was performed under denaturing conditions following the manufacturer's instructions (Qiagen). Proteins were renatured by dialysis against PBS, and detected after SDS-PAGE by Western analysis with an anti-His antibody (Qiagen).
SDS-PAGE and immunoblot analysis were performed as described (Moelleken and Hegemann, 2008). For detection of Pmp216His proteins, monoclonal anti-His antibodies (Qiagen) or a polyclonal anti-Pmp21-E serum (antigen-purified; IgG 87 µg ml−1) (1:250 dilution) was used and visualized with AP-conjugated anti-mouse or anti-rabbit antibodies (Promega). For time-course experiments HEp-2 cells were infected with C. pneumoniae at moi 1. After 12–96 h cells were prepared and analysed by SDS-PAGE using a monoclonal anti-β-actin antibody or anti-Pmp21-E serum (antigen-purified). EBs were gradient-purified after 72 h p.i., and 1 × 107 EBs were resuspended in PBS, or in PBS with 2% Sarcosyl, 2% SDS, 10 mM DTT, and sonicated for 1 min at room temperature (RT). Loading dye and 1 mM DTT were added and samples were boiled for 10 min at 100°C. Prior to loading, samples were pelleted for 1 min at 13 000 r.p.m. and supernatant was loaded. Proteins were detected by the anti-Pmp21-E serum (antigen-purified).
Twenty-four to 90 h p.i. HEp-2 cells on glass coverslips (12 mm diameter) were washed once with PBS, fixed with freshly prepared 3% formaldehyde (diluted from a 30% formaldehyde stock solution, which was prepared by dissolving paraformaldehyde powder in PBS at 65°C) for 30 min at RT and permeabilized with PBS containing 0.2% Triton X-100 or fixed with 96% methanol for 10 min at RT (Vandahl et al., 2002). The monolayer was washed three times with PBS. For detection of chlamydial inclusions or non-fixed C. pneumoniae EBs, either anti-DnaK (Birkelund et al., 1990), anti-OmpA (Dako) or anti-Pmp21-E serum (antigen purified; IgG 87 µg ml−1) (undiluted) was used in combination with Cy3-conjugated anti-mouse antibody (Sigma) or FITC-conjugated anti-rabbit antibody (Dako). For direct staining of inclusions, a monoclonal FITC-conjugated antibody against chlamydial LPS was used (Bio-Rad). Cells were viewed using a Zeiss Axioskop. The microimmunofluorescence (MIF) analysis was performed as described (Moelleken and Hegemann, 2008).
Approximately 5 × 106 yeast cells from 24 h cultures were washed twice with PBS and immobilized on poly-l-lysine-coated glass slides. Slides were incubated with PBS containing 1% BSA followed by incubation with anti-V5 and Cy3-conjugated anti-mouse antibodies (Invitrogen, Sigma).
Yeast adhesion assays were performed with HEp-2 cells as previously described (Moelleken and Hegemann, 2008). Adhesion assays with protein-coated latex beads were performed as described (Dersch and Isberg, 1999). Alternatively, bead binding to HEp-2 cells was quantified by flow cytometry. HEp-2 cells were grown to a confluent monolayer in 24-well plates and incubated with a 10-fold excess of protein-coated latex beads (diameter 1 µm, green fluorescent, Sigma) for 1 h at 37°C. Cells were washed twice with PBS, detached with Cell Dissociation solution (Sigma) and analysed by flow cytometry using a FACSAria (BD Biosciences).
These assays were performed as previously described (Moelleken and Hegemann, 2008). The anti-Pmp21-E serum (total protein content 3 mg ml−1) was used without further purification as outlined in the legend of Fig. 5A. Statistical analysis of the infection inhibition assay was carried out by Student's t-test.
Approximately 2 × 108 purified C. pneumoniae EBs were labelled for 1 h at 37°C with 25 µmol of CFSE (Molecular Probes) and washed twice with PBS containing 1% BSA as previously described (Schnitger et al., 2007). Confluent monolayers of HEp-2 cells grown in 24-well plates were incubated for 4 h at 37°C with 12.5–200 µg ml−1 recombinant protein or 500 µg ml−1 heparin, CFSE-labelled C. pneumoniae EBs (moi 10) were added for 1 h. Cells were then washed with PBS, trypsinized and fixed with formaldehyde, and the efficiency of adhesion was measured by flow cytometry using a FACSAria (BD Biosciences).
We are very grateful to Svend Birkelund for the IF protocol and the anti-DnaK antibody. We thank Frederik Wuppermann for support in the early phase of the project and Gido Murra and Klaus Meyer for help with FACS analysis. This work was supported by the Deutsche Forschungsgemeinschaft, Sonderforschungsbereich 590, project number C5 and Forschergruppe 729, project number 3 (to J.H.H.).
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