Fibronectin-binding protein B variation in Staphylococcus aureus
BMC Microbiology volume 10, Article number: 160 (2010)
Fibronectin binding proteins A and B (FnBPA and FnBPB) mediate adhesion of S. aureus to fibrinogen, elastin and fibronectin. We previously identified seven different isotypes of FnBPA based on divergence in the fibrinogen- and elastin-binding A domains. The variation created differences in antigenicity while ligand binding functions were retained. Here, FnBPB variation was examined in both human and bovine isolates and compared to that of FnBPA.
Seven different fnbB allelic variants were identified. Some strains that cluster by phylogenetic analysis contain different fnbB variants, whereas more divergent strains contain the same fnb B variant. The phylogeny of fnb B alleles does not match the phylogeny of fnbA alleles. Some FnBPA and FnBPB isotypes that are specified by human S. aureus strains are also found in bovine strains. The seven fnb B allelic variants encode seven distinct isotypes of the FnBPB A domain that are 61 to 85% identical in amino acid sequence. Variant amino acid residues were mapped on a three-dimensional model of the FnBPB A domain and were predicted to be surface-exposed. They are responsible for the antigenic diversity detected with polyclonal antibody and a monoclonal antibody raised against isotype I. Ligand binding by recombinant FnBPB N23 isotypes was compared by ELISA-based solid phase assays and surface plasmon resonance. Each bound to immobilized fibrinogen, elastin and fibronectin dose-dependently and saturably with similar affinities. Binding to fibronectin was surprising because the A domains do not contain any known motifs that mediate binding to fibronectin. This raises the possibility that the A domain of FnBPB contains a novel fibronectin binding motif that binds fibronectin by a novel mechanism.
Seven different isoforms of FnBPB A domain retain ligand-binding functions but are antigenically distinct. The variation in FnBPA and FnBPB occurs in human and bovine S. aureus strains and may act as an immune evasion mechanism. All seven isotypes of FnBPB are capable of binding fibronectin though none contain any known fibronectin-binding motifs. These results have implications for the development of vaccines or immunotherapeutics that target FnBPB
Staphylococcus aureus is a commensal that colonizes the moist squamous epithelium of the human anterior nares. Twenty percent of the population are permanently colonised while the remainder are colonized intermittently . It is an important opportunistic pathogen that can cause superficial skin infections as well as invasive life-threatening conditions such as septic arthritis and endocarditis . The success of S. aureus as a pathogen can in part be attributed to the expression of cell surface protein receptors designated MSCRAMMs (m icrobial s urface c omponents r ecognizing a dhesive m atrix m olecules) that interact specifically with proteins present in the host plasma and extracellular matrix . MSCRAMMs act as virulence factors that allow S. aureus to adhere to the surface of host cells and to damaged tissue and help it to avoid phagocytosis by neutrophils [4–6]
The fibronectin binding proteins (FnBPs) A and B of S. aureus are multifunctional MSCRAMMs which recognise fibronectin, fibrinogen and elastin [7–10]. FnBPA and FnBPB have considerable organization and sequence similarity and are composed of a number of distinct domains [7, 9]. Figure 1 illustrates the domain organization of FnBPA and FnBPB of S. aureus strain 8325-4. Both proteins contain a secretory signal sequence at the N-terminus and a C-terminal LPETG motif required for sortase-mediated anchoring of the proteins to the cell wall peptidoglycan. The N-terminal A domains of FnBPA and FnBPB are exposed on the cell surface and promote binding to fibrinogen and elastin [10, 11]. Based on their sequence similarity to the fibrinogen binding A domain of clumping factor A (ClfA) , the A domains of FnBPA and FnBPB are predicted to fold into three sub-domains N1, N2 and N3 similar to ClfA . The A domains of FnBPA, FnBPB and ClfA bind fibrinogen at the C-terminus of the γ-chain [10, 14]. Unlike ClfA, the A domains of FnBPA and FnBPB also bind to elastin . It is proposed that ligand binding occurs through the same dynamic "dock, lock, latch" mechanism that has been predicted for fibrinogen binding to the A domain of ClfA . The fibrinogen γ-chain peptide binds to a groove located between domains N2 and N3 in the apo form. C-terminal residues in domain N3 undergo a conformational change to bind adjacent to a β-strand in domain N2 forming an extra β-strand termed the latching peptide. This traps the fibrinogen peptide in the groove between N2 and N3 and locks it in place .
Located distal to the A domains of FnBPA and FnBPB are unfolded regions which contain multiple, tandemly arranged motifs (Figure 1) that bind to the N-terminal type I modules of fibronectin by a tandem beta-zipper mechanism . The sequences of the fibronectin-binding motifs are highly conserved in FnBPA and FnBPB from strain 8325-4 (95% amino acid identity). By contrast the sequences of the fibrinogen and elastin binding A domains are more divergent (45% amino acid identity).
Most research on fibronectin-binding proteins has been preformed with FnBPA from strain 8325-4. It was reported previously that the A domain of FnBPA of S. aureus strain 8325-4 comprising residues 37-544 bound to immobilized elastin and to fibrinogen (Figure 1.) [8, 10]. The A domain co-ordinates were revised recently and it was noted that the C- terminus of rFnBPA37-544 likely contained a single fibronectin-binding motif . The ability of this protein to bind fibronectin was later confirmed . In the same study, the revised A domain of FnBPA spanning residues 194-511 (Figure 1) was shown bind fibrinogen and elastin but not fibronectin. The minimum region of the FnBPA A domain needed for binding to fibrinogen and elastin is subdomains N23 (residues 194-511). The N1 sub-domain is not required for ligand binding .
The binding of FnBPs to fibronectin promotes the internalization of S. aureus into epithelial and endothelial cells which are not normally phagocytic [17, 18]. FnBP-mediated invasion occurs through the formation of a fibronectin bridge between S. aureus and the α5β1 integrin . This may promote bacterial dissemination from the bloodstream to internal organs and evasion of immune responses and antibiotics. This was convincingly demonstrated in a study of the role of FnBPA in experimental endocarditis where binding to both fibrinogen and fibronectin required. Binding of fibrinogen was required for initial colonization of thrombi on damaged valves and while binding to fibronectin was required for the infection to spread .
FnBPA and FnBPB are encoded by two closely linked but separately transcribed genes, fnbA and fnbB [7, 9]. While most strains contain both genes, some strains contain only fnbA . In strain 8325-4, studies with site-specific fnbA and fnbB insertion mutants showed that either FnBPA or FnBPB mediated adherence to immobilized fibronectin but there was no significant difference in adherence between wild type strains and single fnb mutants . However, studies with clinical isolates suggested that strain associated with invasive diseases are significantly more likely to have two fnb genes .
Seven variants (isotypes I-VII) of FnBPA were identified based on divergence in the amino acid sequences of the minimal ligand-binding N23 sub-domains . Each FnBPA isotype retained ligand-binding activity but were antigenically distinct. Modelling the 3D structures showed that the amino acid variation occurred in surface-exposed residues and not in those involved in ligand-binding .
The initial aim of this study was to characterize the A domain of FnBPB and to determine the extent of variation in the A domain. It was discovered that the A domain of all FnBPB isotypes had the ability to bind to fibronectin by a novel mechanism.
fnbB gene variation in S. aureus whole-genome sequences
Previously we reported that the A domain of FnBPA from strain P1 varied substantially from that of strain 8325-4, sharing only 73.5% amino acid identity . We then identified seven variants of FnBPA A domain (isotypes I-VII) based on divergence in the minimal ligand-binding N23 sub-domain. Each recombinant N23 variant was shown to retain ligand-binding function but was antigenically distinct . This prompted us to investigate variation in the A domain of the second fibronectin-binding protein, FnBPB.
DNA encoding the entire FnBPB A domain of strain P1 was amplified by PCR and sequenced. The deduced amino acid sequence was compared with that of strain 8325-4 and the overall identity was 80%. The A domain sequences of FnBPB from published S. aureus genomes were compared to determine if diversity in this domain is common amongst S. aureus isolates. All of the sequenced strains, except strain MRSA252 and the bovine strain RF122, contain genes encoding both FnBPA and FnBPB. Strains MRSA252 and RF122 both encode the FnBPA protein. The amino acid sequence of the A domain of FnBPB from S. aureus strains 8325-4, COL, USA300, Mu50, MSSA476, N315, MW2 and P1 were compared by pair-wise alignments and the identities calculated. Strains that are closely related and belonging to the same clonal complex were found to share identical A domains. However, comparison of A domain sequences of strains from different sequence types revealed that significant diversity exists. While subdomain N1 is highly conserved in all strains (94-100% amino acid identity) the N2 and N3 domains from unrelated isolates are significantly more divergent. Based on the sequences of the N23 subdomains, four variants of FnBPB (isotypes I-IV) were identified that share 61.1 - 80.6% amino acid identity (Table 1).
DNA hybridization analysis using fnbB isotype-specific probes
To determine the distribution of FnBPB A domain isotypes I - IV in S. aureus strains of different MLSTs and to identify any novel A domain isotypes, DNA hybridization was used with isotype-specific probes homologous to DNA specifying a portion of the highly divergent N3 sub-domain. DNA encoding the entire A domain was amplified with A domain flanking primers. PCR products were then spotted onto membranes and hybridized with the DIG-labelled type-specific probes. An example of the hybridization experiments with probes I - IV is shown in Figure 2. The probes were shown to be type-specific because each only hybridized to the appropriate control fnbB fragment (Figure 2A-D, top rows). fnbB DNA from S. aureus strains 2 (ST7),114 (ST39), 233 (ST45), 304 (ST39), 138 (ST30), 563 (ST37), 3077 (ST17) and 3110 (ST12) did not hybridise to any of the probes, indicating that they may specify novel FnBPB isotypes or lack the fnbB gene.
Identification of novel FnBPB isotypes (Types V, VI and VII)
The fnbB gene fragments amplified from S. aureus strains 2 (ST7) 114 (ST39), 233 (ST45), 304 (ST39), 138 (ST30), 563 (ST37), 3077 (ST17) and 3110 (ST12) did not hybridise to probes specific for FnBPB isotypes I-IV. The fnbB gene fragments from these strains were cloned and sequenced, and the deduced A domain amino acid sequences were compared to the sequences of A domains of types I - IV. S. aureus strains 2 (ST7) and 3110 (ST12) specify a novel FnBPB A domain called isotype V (N23, 68.8 - 73.3% identical to isotypes I - IV). The A domains of strains 3077 (ST17) and 233 (ST45) are also different and are called isotype VI (N23, 66.0- 76.6% identical to types I - V) and isotype VII (N23, 66.2% - 85% identical to types I-VI) (Table 1). Strains 114, 563, 138 and 304 specify an identical A domain which is 92% identical to isotype II and is called isotype II* (Table 1)
Phylogenetic analysis of FnBPB A domain isotypes I-VII
Figure 3 shows a neighbour-joining phylogenetic tree which was constructed based upon the concatenated sequences of the seven housekeeping genes used for MLST analysis. As MLST reflects the evolution of the stable core genome , this tree describes the phylogenetic relatedness of the S. aureus strains studied here. It is separated into two major clusters as was also shown previously in a detailed phylogenetic analysis of thirty diverse S.aureus isolates . The FnBPB A domain isotypes specified by each genotype (as predicted by DNA hybridisation or sequencing) are indicated. The phylogeny of fnbB alleles illustrated here does not correspond to that of the core genome as determined by MLST. For example, two strains that cluster together in Group 1 (ST49 and ST52) carry fnbB genes encoding isotype II, as do distantly related strains from Group 2 (ST5 and ST18). Conversely, clustered strains such as ST8 and ST97 from Group 2 contain fnbB genes encoding isotypes I and IV, respectively. Isolates belonging to the same ST (ST45) were found to specify different FnBPB isotypes (II and VII). These results suggest that fnbB alleles have dispersed by horizontal transfer, most likely by homologous recombination.
It has been recently reported that strains 116 (ST9) and 3077 (ST17) specify an identical FnBPA A domain called isotype II . In this study, these strains were found to specify different FnBPB A domains, isotypes II and VI respectively. This indicates that the phylogeny of fnbB alleles does not match that of fnbA alleles despite the two genes being closely linked.
FnBP isotypes encoded by bovine S. aureus strains
We expanded the investigation into FnBP variation to include FnBPs from a variety of bovine S. aureus strains. Nineteen bovine isolates representing genetically unrelated strains were screened to determine if they specified the same FnBP isotypes as human strains. This strain collection included strain RF122, the genome of which has been sequenced . RF122 contains only one fnb gene encoding FnBPA.
DNA encoding fnbA was amplified from the genomic DNA of each strain using generic A domain primers. PCR products hybridised to FnBPA probes specific for isotypes I, II, III or IV. Similarly fnbB DNA was amplified by PCR from the genomic DNA of all strains except RF122. These PCR products hybridised to FnBPB probes specific for isotype I, II, III, IV or V. These results indicate that the FnBP isotypes which are expressed by human strains are also specified by bovine strains. Furthermore, the results of this study suggest that the lack of fnbB in the genome of strain RF122 is not characteristic of all bovine strains. None of the strains tested specify FnBPA or FnBPB isotypes V, VI or VII.
Figure 4 shows a neighbour-joining phylogenetic tree which was constructed based on MLST data as described above. The FnBPA and FnBPB A domain isotypes specified by each genotype are included. The distribution of fnbB and fnbA variants does not correlate with the genetic relatedness of the strains as determined by MLST. The phylogeny of fnb alleles carried by bovine S. aureus isolates is therefore very similar to that of human strains.
Generation of 3D-models for FnBPB (N23) types I-VII and mapping the location of variant amino acid residues
Theoretical models of the structure of region A (N23) of FnBPB isotypes I-VII were generated based on the crystal structure of the equivalent domains of the S. aureus clumping factor ClfA. A ligand-binding trench is predicted to form between the N2 and N3 domains of FnBPB. C-terminal residues in sub-domain N3 are predicted to form the putative latching peptide. In each of the seven molecular models, the variant residues mapped to the surface of the protein while the residues within the predicted ligand-binding trench are highly conserved (Figure 5.). The predicted 3D structure obtained for FnBPB type I of strain 8325-4 and the predicted location of variant residues is shown in Figure 4. Residues 467-480 of FnBPB isotype I comprise the predicted latching peptide and are shown here in blue. In the crystal structure of the apo form of ClfA the latching peptide is folded over the N3 subdomain.
Antigenic variation: binding of antibodies to isotypes I-VII
We previously demonstrated that variation in the A domain of FnBPA resulted in proteins that are antigenically distinct. Here the ability of polyclonal anti-isotype I antibodies and a monoclonal anti-isotype I antibody to bind different recombinant FnBPB N23 isotypes was measured by ELISA. Polyclonal rabbit anti-isotype I antibodies had a 4 - 9 fold lower affinity at half maximum binding for isotypes II - VII compared to isotype I (Figure 6). This suggests that amino acid variation creates differences in surface-exposed epitopes on the A domain molecule that affect immuno-crossreactivity. Mouse monoclonal antibody 2E11 bound efficiently to isotype I but showed little binding to isotypes II - VII as shown in Figure 5. This suggests that the 2E11 epitope is only present on isotype I.
Binding of FnBPB A domains isotypes I - VII to immobilized ligands (ELISA)
Each recombinant N23 isotype bound to immobilized fibrinogen and elastin in a dose-dependent and saturable manner as shown in Figure 7. The estimated half maximum binding concentrations were 0.5 μM and 0.9 μM respectively. These results confirm that the revised co-ordinates of the N23 subdomain of region A of FnBPB (isotypes I-VII) is sufficient for ligand-binding and that subdomain N1 is not required.
Somewhat surprisingly, the seven N23 isotypes also bound fibronectin dose-dependently and saturably with a half-maximum binding concentration of 1.5 μM (Figure 7c). Recombinant FnBPA isotype I, which was previously shown not to bind fibronectin, was a used was as a negative control. The ability of the FnBPB A domain proteins to bind fibronectin was surprising because the amino acid sequences do not contain any known fibronectin-binding motifs.
Measuring the affinity of FnBPB A domain isotype I for fibrinogen, elastin and fibronectin by surface plasmon resonance
The results of the solid-phase binding assays suggested that the A domain of FnBPB binds fibrinogen, elastin and fibronectin with similar affinity. Estimated half maximal binding concentrations were in the low micromolar range. To verify these results, the affinities of rN23 isotype I for fibrinogen, elastin and fibronectin were measured using Surface Plasmon Resonance. Human fibrinogen, elastin and fibronectin were immobilized onto the surface of dextran chips. rN23 type I protein was passed over the surface in concentrations ranging from 0.15 μM to 10 μM. The representative sensorgrams shown in Figure 8 have been corrected for the response obtained when recombinant protein was flowed over uncoated chips. The K D for the interaction with fibrinogen, elastin and fibronectin was 2 μM, 3.2 μM and 2.5 μM, respectively.
The colonization of host tissue by S. aureus is an important factor in disease pathogenesis. S. aureus expresses on its cell surface a number of MSCRAMMS that promote colonization of diverse sites and contribute to virulence. Most S. aureus strains can express two distinct fibronectin-binding proteins (FnBPA and FnBPB). These two multifunctional MSCRAMMs both mediate adhesion to fibrinogen, elastin and fibronectin.
FnBPA and FnBPB are encoded by the two closely linked genes, fnbA and fnbB . It has been reported that the fnbA and fnbB genes from 50 different strains representing the major MRSA clones found in Europe have undergone greater sequence divergence than genes encoding other surface proteins such as clfA and clfB . Analysis of the fnb genes from published genome sequences showed that divergence was confined to the region encoding the N-terminal fibrinogen and elastin-binding A domains while the C-terminal fibronectin-binding motifs were highly conserved ( and this study). Our previous study identified seven isotypes of FnBPA based on divergence in the minimal ligand-binding N23 sub-domain . Each recombinant isotype was found to retain ligand-binding function but was antigenically distinct.
This study aimed to investigate the divergence in the A domain of FnBPB and to determine if variation in this region of the protein is widespread amongst S. aureus strains. The fnbB gene sequences from sequenced S. aureus strains and strain P1 were compared. Four FnBPB variants (isotypes I-IV) were identified based on divergence in N23 sub-domains, which are 66-76% identical to one another.
In order to determine the distribution of FnBPB isotypes I-IV and to identify novel isotypes, type specific probes were generated and used to screen fnbB DNA from a variety of clonal types using a well-characterized strain collection of human origin and human isolates where genomes have been fully sequenced . Three novel FnBPB isotypes were identified (types V, VI and VII) which are 61.1% - 85% identical to isotypes I-IV. Phylogenetic analysis of FnBPB isotypes indicated that the phylogeny of fnbB alleles does not correlate with the core genome as reflected by MLST. The evolution of S. aureus has been predominantly clonal where alleles are 5- to 10-fold more likely to diversify by point mutations than by recombination . The distribution of fnbB alleles amongst different S. aureus lineages suggests, however, that recombination has been involved. Horizontal transfer by homologous recombination is likely to be responsible for the dispersal of genes encoding the same isotypes across strains of different phylogenies. The distribution of fnbA alleles described in the study by Loughman et al does not match the distribution of fnbB alleles described here . Different combinations of FnBPA and FnBPB isotypes are specified by strains that cluster phylogenetically. For example, strains belonging to ST12 were shown to specify FnBPB Type V and FnBPA Type V. By contrast, strains belonging to ST13 specified FnBPB Type IV and FnBPA Type V. This suggests that the phylogeny of fnbB alleles has evolved independently from that of fnbA alleles and has involved separate recombination events despite the genes being closely linked.
Our study of FnBP variation in S. aureus was extended here to include bovine S. aureus strains. The genome of the bovine strain RF122 contains only the fnbA gene but lacks fnbB. Using generic primers, DNA encoding FnBPA and FnBPB was amplified from genomic DNA of nineteen bovine S. aureus strains. The amplification of fnbB DNA from these strains indicates that the lack of the fnbB gene in strain RF122 is not common to all bovine S. aureus strains. The fnbA and fnbB PCR products were subsequently probed with DNA probes specific for A domain isotypes specified by human S. aureus strains. It was shown that bovine isolates specify the some of the same isotypes of FnBPA and FnBPB as those specified by human isolates. The distribution of isotypes across the population of bovine strains tested was found to be uneven. No strains tested specified FnBPA isotypes V, VI or VII or FnBPB isotypes VI or VII. The majority of the strains tested were found to specify FnBPA Type IV and FnBPB Type II. Interestingly in the study of Loughman et al, FnBPA Type II was found to be predominant in human clinical isolates . It could be postulated that this difference in FnBPA isotype frequency reflects the differences in selective pressures posed by these two distinct host immune systems.
Further evidence for the role of recombination in the evolution of S.aureus comes from the genome structure of ST239 strains which are composed of 557 kb of ST8 DNA spliced into 2,220 kb of an ST30 strain . Also, the gene for coagulase has undergone similar diversification as the fnb genes . Recombination within coa genes encodeding ten major isotypes has created novel subtypes and there is evidence for the same coa isotype being expressed by strains with different genetic backgrounds suggesting horizontal dissemination by homologous recombination .
A 3D molecular model of the N2 and N3 domains of FnBPB was generated based on the known structure of ClfA. Like the A domain of ClfA (and FnBPA) it is predicted that the N23 subdomain of FnBPB represents the minimal ligand binding region and a ligand binding trench is predicted to form between the N2 and N3 subdomains. Based on this model, it was shown that the majority of variant residues are located on the surface of the protein while residues that are predicted to be involved in ligand-binding are highly conserved. Amino acid sequence variation affected antibody recognition. Polyclonal antibodies against isotype I had reduced affinity for isotypes II - VII while a monoclonal antibody raised against isotype I had little or no affinity for all other isotypes. As with FnBPA isotypes, FnBPB sequence variation has created different epitopes on the A domains that affect immunocross-reactivity. This result is consistent with the predicted location of variant residues on the surface of the protein and not in regions involved in ligand binding.
While most strains contain both genes, some strains contain only fnbA . Studies with site-specific fnbA and fnbB insertion mutants of strain 8325-4 have shown that either FnBPA or FnBPB can mediate adherence to immobilized fibronectin, but there was no difference in adherence between wild type strains and single fnb mutants, indicating functional redundancy . However, isolates associated with invasive diseases are significantly more likely to have two fnb genes . Combined antigenic variation in both FnBPA and FnBPB may be employed by S. aureus to thwart the host immune responses during colonization or invasive infection. Interestingly, the diversity which occurs in the N2 and N3 subdomains of FnBPA and FnBPB does not occur in the N1 subdomain of either protein. For both FnBP proteins, the N1 subdomain is not required for ligand binding, similar to ClfA . The A domain of both ClfA and another S. aureus fibrinogen binding protein, clumping factor B (ClfB), are susceptible to cleavage by aureolysin at a SLAVA/SLAAVA motif located between subdomains N1 and N2 . A SLAVA-like motif occurs in both FnBP proteins with S177ADVA181 and S144TDVTA149 present in FnBPA isotype I and FnBPB isotype I, respectively, which may render the A domains similarly susceptible to proteolysis. Perhaps the highly conserved N1 subdomains are less readily recognized by the host immune system and may function to protect the ligand-binding N2N3 during early stages of infection.
The ligand binding ability of recombinant FnBPB N23 subdomain isotypes I-VII was compared by ELISA-based solid phase binding assays. Each A domain isotype bound to immobilized fibrinogen and elastin with similar affinities. These results confirm that like the A domains of ClfA and FnBPA, the N23 subdomain of FnBPB is sufficient for ligand-binding and that the N1 subdomain is not required for ligand-binding. The results also suggest that these ligand-binding functions are biologically important and are consistent with the predicted location of variant residues on the surface of the protein and not in regions predicted to be involved in ligand binding. Using the recombinant N23 isotype I protein as a prototype, the affinity of FnBPB for fibrinogen and elastin was analysed by SPR. The K D for both interactions was in the low micro molar range.
Somewhat surprisingly, the seven recombinant N23 FnBPB isotypes examined in this study bound immobilized fibronectin with similar affinity. The interaction between rN23 Type I (residues 162-480) was verified by SPR analysis with a K D in the low micro molar range. The results of these fibronectin-binding assays are surprising because this region of FnBPB does not contain any known fibronectin-binding motifs suggesting that the A domains of FnBPB (isotypes I-VII) contain a novel fibronectin-binding motif and may bind fibronectin by a novel mechanism. Experiments are currently underway to examine the biological significance of fibronectin-binding by the A domain of FnBPB and to determine a mechanism for this interaction and identify the FnBPB binding region(s) in human fibronectin.
We have identified seven isotypes of the N terminal A domain of FnBPB in a genetically diverse collection of human S. sureus strains. Amino acid variation creates differences in immuno-crossreactivity while ligand-binding functions are maintained. This may contribute to immune evasion by S. aureus. The distribution of FnBPB isotypes throughout the S. aureus population is random but does not correlate with the random distribution of FnBPA isotypes described previously. This suggests that fnbA and fnbB alleles have been dispersed independently by horizontal transfer which most likely involved homologous recombination. Four of the seven FnBPB isotypes were also identified in bovine S. aureus strains. The lack of fnbB in strain RF122 is not common to all bovine strains. All seven recombinant A domain isotypes bound fibronectin with a K D in the low micro molar range. This raises the possibility that the A domain of FnBPB binds fibronectin by a novel mechanism. These data have implications for the FnBPB A domain as a target for a vaccine or immunotherapeutics.
Bacterial strains and growth conditions
Escherichia coli strains were cultivated on L-agar and L-broth with shaking at 37°C. Cloning was routinely performed in E. coli strain XL-1 Blue (Stratagene). E. coli strain TOPP 3 (Qiagen) was used for the expression of recombinant FnBPB A domain proteins. Ampicillin (100 μg ml-1) was incorporated into growth media where appropriate. The Staphylococcus aureus strains used in this study are listed in Table 2 and were cultivated on trypticase soy agar (TSA) or broth (TSB). Human S. aureus strains from individuals from Oxfordshire, U.K have been characterized by multi-locus sequence typing (MLST) . Strain P1 is a rabbit virulent strain  and has been characterised by MLST . Bovine S.aureus strains were a kind gift from Cyril Smyth (Trinity College, Dublin). They were isolated from geographically diverse locations and were characterized by MLST .
Plasmid DNA was isolated using the Wizard® Plus SV Miniprep kit (Promega) according to manufacturer's instructions and finally transformed into E. coli XL1-Blue cells using standard procedures . Chromosomal DNA was extracted using the Bacterial Genomic DNA purification kit (Edge Biosystems). Restriction digests and ligations were carried out using enzymes from New England Biolabs and Roche according to the manufacturers' protocols. Oligonucleotides were purchased from Sigma-Genosys and are listed in Table 3. DNA purification was carried out using the Wizard® SV Gel and PCR Clean-up System (Promega).
Cloning of fnbB gene fragments
Generic primers, corresponding to conserved DNA encoding the signal sequence and fibronectin binding domain 2, were designed from conserved sequences in fnbB genes from publicly available S. aureus genomes. PCR products were cleaved with BamHI restriction sites incorporated into the primers, ligated to BamHI- cleaved pBluescript DNA and transformed into E. coli. The cloned fnbB gene fragments were sequenced using T3 and T7 primers by GATC Biotech AG (Germany).
DNA hybridisation using fnbB type-specific probes
DIG-labelled isotype-specific probes were synthesised by PCR. Primers were designed to amplify a small region of DNA (~300 bp) in the N3 sub-domain of isotypes I-VII. The PCR products were labelled by incorporating DIG-labelled dNTPs (Roche). Five ng of DNA encoding the A domain of FnBPB from clinical isolates was spotted onto positively charged nylon membranes (Roche) and allowed to air-dry. Membranes were incubated for 5 min on blotting paper soaked in denaturation solution (1.5 M NaCl, 0.5 M NaOH), 5 min in neutralization solution (1.5 M NaCl, 1 M Tris-HCl, pH 7.4), and finally for 15 min on blotting paper soaked with 2× SSC solution (300 mM NaCl, 30 mM tri-sodium citrate). DNA was fixed on the membranes by incubation at 120°C for 30 min. Membranes were incubated for 2 h at 68°C in pre-hybridization solution (5× SSC, 0.1% w/v N-lauroylsarcosine, 0.02% w/v SDS and 1× Blocking Reagent (Roche). DIG-labelled probes were denatured by heating at 95°C for 10 min, diluted in pre-hybridization solution and incubated with nylon membranes for 18 h at 68°C. Following hybridization, the membranes were washed twice with 2× SSC/0.1% w/v SDS at room temperature followed by two washes with 0.5× SSC/0.1% w/v SDS at 68°C for 20 min. Membranes were equilibrated for 30 min in maleic acid buffer (100 mM maleic acid, 150 mM NaCl, pH 7.5), and bound DIG-labelled probes were detected by incubation for 30 min with alkaline phosphatase-conjugated anti-DIG antibody (Roche) diluted 1:10,000 in maleic acid buffer. After washing twice with maleic acid buffer containing 0.3% v/v Tween 20, the chemiluminescence substrate CSPD (Roche) was used to detect bound anti-DIG antibodies and membranes were exposed to X-OMAT UV Plus Film (Kodak).
Bioinformatic and phylogenetic analysis of FnBPB A domain isotypes
Protein sequences were aligned in pairwise combinations to calculate amino acid identity using the ExPASY SIM alignment tool http://www.expasy.org/tools/sim-prot.html. The concatenated MLST allele sequences of S. aureus strains were downloaded from the MLST database http://saureus.mlst.net/. A phylogenetic analysis of concatenated MLST allele sequences was conducted using MEGA version 4 . Alignments of multiple protein sequences to view areas of conservation amongst A domains were performed using Clustal W http://www.ebi.ac.uk/
Generation of 3D-models for FnBPB (N23) types I-VII
Theoretical models of the structure of region A (N23) types I-VII were obtained by submitting the amino acid sequences for this segment of each protein to the Phyre service of the 3D-PSSM website http://www.sbg.bio.ic.ac.uk/phyre/. This web-based tool models the structure of these sequences based structure of the equivalent domains of the S. aureus clumping factor ClfA. All structures were viewed using the pyMOL viewing software.
Expression of recombinant FnBPB A domain proteins
Primers were designed to amplify DNA encoding residues 162-480 (N23 sub-domain) of FnBPB isotype I from strain 8325-4 by PCR. The primers included BamHI and SmaI restriction sites to facilitate cloning into the multiple cloning site of the N-terminal six-histidine tag expression vector pQE30 (Qiagen) and incorporated a 3' stop codon. The equivalent N23 regions of FnBPB isotypes types II-VII were PCR-amplified from strains N315, MSSA476, P1, 2, 3077 and 233, respectively. The PCR products were cloned separately into pQE30 and transformed into E. coli cells for protein production. Each construct was verified by sequencing (GATC Biotech AG, Germany) and proteins were purified by Ni2+ chelate chromatography . Concentrations were determined using the BCA Protein Assay Kit (Pierce). Proteins were dialysed against PBS for 24 h at 4°C, aliquoted and stored at -70°C.
Direct binding of recombinant FnBPB A domain proteins to immobilized elastin, fibrinogen and fibronectin
Human aortic elastin (Elastin Products Company; 50 μg/ml) was coated onto microtiter wells for 18 hr under UV light. Wells coated with human fibrinogen (Calbiochem; 10 μg/ml), and fibronectin (Calbiochem; 10 μg/ml) were placed at 4°C overnight. All plates were blocked with 5% skimmed milk in phosphate buffered saline (PBS) for 2 hr at 37°C. Following three washes with PBS containing 0.05% v/v Tween 20 (PBST) various concentrations of purified rFnBPB N23 constructs in PBS were added and incubated at 37°C for 2 hr. After three washes with PBST, bound protein was detected by incubation with a 1:500 dilution of monoclonal antibody 7E8 that recognizes the N-terminal hexahistidine fusion tag. After 1 h incubation with shaking at room temperature, the wells were washed three times with PBST followed by 100 μl per well of goat-anti-mouse IgG antibodies conjugated to horseradish-peroxidase (HRP, Dako; Denmark) diluted 1:2000. After incubation for 1 h at room temperature, wells were washed three times with PBST, and bound HRP-conjugated antibodies were detected with 10 μg per well of 3,3',5,5'-tetramethylbenzidine (TMB; Sigma) in 0.05 M phosphate-citrate buffer containing 0.006% (v/v) hydrogen peroxide. After incubation at room temperature for 5 min the reaction was stopped by adding 50 μl of 2 M H2SO4. The absorbance at 450 nm was measured with an ELISA plate reader (Multiskan EX, Labsystems).
The purity of the commercial fibronectin used in these assays was examined by SDS-PAGE. ELISA experiments with anti-fibrinogen antibodies revealed that the fibronectin was free of fibrinogen contamination.
Various concentrations of recombinant FnBPB A domain proteins in PBS were coated onto Nunc 96-well microtitre dishes for 18 h at 4°C. Wells were washed and blocked with BSA for 2 h as described above. Following three washes with PBST, 100 μl of anti-FnBPB A domain antibodies diluted in BSA-PBST (1.8 μg polyclonal IgG ml-1; 2.5 μg monoclonal IgG ml-1) were added to each well and incubated for 1 h at room temperature with shaking. Polyclonal antibody raised against the isotype I N23 domain of FnBPB was obtained by immunizing specific pathogen-free rabbits with rFnBPB37-480 from S. aureus 8325-4. Monoclonal antibody 12E11 was generated by immunizing mice with recombinant isotype I FnBPB37-480. After 1 h incubation the wells were washed three times with PBST. Goat anti-rabbit IgG-HRP conjugated antibodies or goat anti-mouse IgG-HRP conjugated antibodies (Dako, Denmark), each diluted 1:2000 in BSA-PBST, were added to the wells and incubated for 1 h. After washing three times with PBST, bound HRP-conjugated antibodies were detected as described above.
Analysis of fibrinogen, elastin and fibronectin binding by surface plasmon resonance
Surface plasmon resonance (SPR) was preformed using the BIAcore ×100 system (GE Healthcare). Human fibrinogen (Calbiochem), aortic elastin (Enzyme Research Laboratories) and fibronectin (Calbiochem) were covalently immobilized on CM5 sensor chips using amine coupling. This was performed using 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDC), followed by N-hydroxysuccinimide (NHS) and ethanolamine hydrochloride, as described by the manufacturer. Fibrinogen (50 μg/ml), elastin (50 μg/ml) and fibronectin (50 μg/ml) were dissolved in 10 mM sodium acetate at pH 4.5 and immobilized on separate chips at a flow rate of 30 μl/min in PBS (Gibco). Each chip contained a second flow cell, which was uncoated to provide negative controls. All sensorgram data presented were subtracted from the corresponding data from the blank cell. The response generated from injection of buffer over the chip was also subtracted from all sensorgrams. Equilibrium dissociation constants (Kd) were calculated using the BIA ×100 evaluation software version 1.0.
van Belkum A, Verkaik NJ, de Vogel CP, Boelens HA, Verveer J, Nouwen JL, Verbrugh HA, Wertheim HF: Reclassification of Staphylococcus aureus nasal carriage types. J Infect Dis. 2009, 199 (12): 1820-1826. 10.1086/599119.
Fowler VG, Miro JM, Hoen B, Cabell CH, Abrutyn E, Rubinstein E, Corey GR, Spelman D, Bradley SF, Barsic B: Staphylococcus aureus endocarditis: a consequence of medical progress. JAMA. 2005, 293 (24): 3012-3021. 10.1001/jama.293.24.3012.
Patti JM, House-Pompeo K, Boles JO, Garza N, Gurusiddappa S, Hook M: Critical residues in the ligand-binding site of the Staphylococcus aureus collagen-binding adhesin (MSCRAMM). J Biol Chem. 1995, 270 (20): 12005-12011. 10.1074/jbc.270.20.12005.
Gomez MI, Lee A, Reddy B, Muir A, Soong G, Pitt A, Cheung A, Prince A: Staphylococcus aureus protein A induces airway epithelial inflammatory responses by activating TNFR1. Nat Med. 2004, 10 (8): 842-848. 10.1038/nm1079.
Thakker M, Park JS, Carey V, Lee JC: Staphylococcus aureus serotype 5 capsular polysaccharide is antiphagocytic and enhances bacterial virulence in a murine bacteremia model. Infect Immun. 1998, 66 (11): 5183-5189.
Higgins J, Loughman A, van Kessel KP, van Strijp JA, Foster TJ: Clumping factor A of Staphylococcus aureus inhibits phagocytosis by human polymorphonuclear leucocytes. FEMS Microbiol Lett. 2006, 258 (2): 290-296. 10.1111/j.1574-6968.2006.00229.x.
Jonsson K, Signas C, Muller HP, Lindberg M: Two different genes encode fibronectin binding proteins in Staphylococcus aureus. The complete nucleotide sequence and characterization of the second gene. Eur J Biochem. 1991, 202 (3): 1041-1048. 10.1111/j.1432-1033.1991.tb16468.x.
Roche FM, Downer R, Keane F, Speziale P, Park PW, Foster TJ: The N-terminal A domain of fibronectin-binding proteins A and B promotes adhesion of Staphylococcus aureus to elastin. J Biol Chem. 2004, 279 (37): 38433-38440. 10.1074/jbc.M402122200.
Signas C, Raucci G, Jonsson K, Lindgren PE, Anantharamaiah GM, Hook M, Lindberg M: Nucleotide sequence of the gene for a fibronectin-binding protein from Staphylococcus aureus: use of this peptide sequence in the synthesis of biologically active peptides. Proc Natl Acad Sci USA. 1989, 86 (2): 699-703. 10.1073/pnas.86.2.699.
Wann ER, Gurusiddappa S, Hook M: The fibronectin-binding MSCRAMM FnbpA of Staphylococcus aureus is a bifunctional protein that also binds to fibrinogen. J Biol Chem. 2000, 275 (18): 13863-13871. 10.1074/jbc.275.18.13863.
Keane FM, Loughman A, Valtulina V, Brennan M, Speziale P, Foster TJ: Fibrinogen and elastin bind to the same region within the A domain of fibronectin binding protein A, an MSCRAMM of Staphylococcus aureus. Mol Microbiol. 2007, 63 (3): 711-723. 10.1111/j.1365-2958.2006.05552.x.
McDevitt D, Francois P, Vaudaux P, Foster TJ: Identification of the ligand-binding domain of the surface-located fibrinogen receptor (clumping factor) of Staphylococcus aureus. Mol Microbiol. 1995, 16 (5): 895-907. 10.1111/j.1365-2958.1995.tb02316.x.
Deivanayagam CC, Wann ER, Chen W, Carson M, Rajashankar KR, Hook M, Narayana SV: A novel variant of the immunoglobulin fold in surface adhesins of Staphylococcus aureus: crystal structure of the fibrinogen-binding MSCRAMM, clumping factor A. EMBO J. 2002, 21 (24): 6660-6672. 10.1093/emboj/cdf619.
McDevitt D, Nanavaty T, House-Pompeo K, Bell E, Turner N, McIntire L, Foster T, Hook M: Characterization of the interaction between the Staphylococcus aureus clumping factor (ClfA) and fibrinogen. Eur J Biochem. 1997, 247 (1): 416-424. 10.1111/j.1432-1033.1997.00416.x.
Ganesh VK, Rivera JJ, Smeds E, Ko YP, Bowden MG, Wann ER, Gurusiddappa S, Fitzgerald JR, Hook M: A structural model of the Staphylococcus aureus ClfA-fibrinogen interaction opens new avenues for the design of anti-staphylococcal therapeutics. PLoS Pathog. 2008, 4 (11): e1000226-10.1371/journal.ppat.1000226.
Schwarz-Linek U, Werner JM, Pickford AR, Gurusiddappa S, Kim JH, Pilka ES, Briggs JA, Gough TS, Hook M, Campbell ID: Pathogenic bacteria attach to human fibronectin through a tandem beta-zipper. Nature. 2003, 423 (6936): 177-181. 10.1038/nature01589.
Peacock SJ, Foster TJ, Cameron BJ, Berendt AR: Bacterial fibronectin-binding proteins and endothelial cell surface fibronectin mediate adherence of Staphylococcus aureus to resting human endothelial cells. Microbiology. 1999, 145 (Pt 12): 3477-3486.
Sinha B, Francois PP, Nusse O, Foti M, Hartford OM, Vaudaux P, Foster TJ, Lew DP, Herrmann M, Krause KH: Fibronectin-binding protein acts as Staphylococcus aureus invasin via fibronectin bridging to integrin alpha5beta1. Cell Microbiol. 1999, 1 (2): 101-117. 10.1046/j.1462-5822.1999.00011.x.
Que YA, Francois P, Haefliger JA, Entenza JM, Vaudaux P, Moreillon P: Reassessing the role of Staphylococcus aureus clumping factor and fibronectin-binding protein by expression in Lactococcus lactis. Infect Immun. 2001, 69 (10): 6296-6302. 10.1128/IAI.69.10.6296-6302.2001.
Peacock SJ, Day NP, Thomas MG, Berendt AR, Foster TJ: Clinical isolates of Staphylococcus aureus exhibit diversity in fnb genes and adhesion to human fibronectin. J Infect. 2000, 41 (1): 23-31. 10.1053/jinf.2000.0657.
Greene C, McDevitt D, Francois P, Vaudaux PE, Lew DP, Foster TJ: Adhesion properties of mutants of Staphylococcus aureus defective in fibronectin-binding proteins and studies on the expression of fnb genes. Mol Microbiol. 1995, 17 (6): 1143-1152. 10.1111/j.1365-2958.1995.mmi_17061143.x.
Loughman A, Sweeney T, Keane FM, Pietrocola G, Speziale P, Foster TJ: Sequence diversity in the A domain of Staphylococcus aureus fibronectin-binding protein A. BMC Microbiol. 2008, 8: 74-10.1186/1471-2180-8-74.
Lindsay JA, Holden MT: Staphylococcus aureus: superbug, super genome?. Trends Microbiol. 2004, 12 (8): 378-385. 10.1016/j.tim.2004.06.004.
Cooper JE, Feil EJ: The phylogeny of Staphylococcus aureus - which genes make the best intra-species markers?. Microbiology. 2006, 152 (Pt 5): 1297-1305. 10.1099/mic.0.28620-0.
Guinane CM, Sturdevant DE, Herron-Olson L, Otto M, Smyth DS, Villaruz AE, Kapur V, Hartigan PJ, Smyth CJ, Fitzgerald JR: Pathogenomic analysis of the common bovine Staphylococcus aureus clone (ET3): emergence of a virulent subtype with potential risk to public health. J Infect Dis. 2008, 197 (2): 205-213. 10.1086/524689.
Kuhn G, Francioli P, Blanc DS: Evidence for clonal evolution among highly polymorphic genes in methicillin-resistant Staphylococcus aureus. J Bacteriol. 2006, 188 (1): 169-178. 10.1128/JB.188.1.169-178.2006.
Feil EJ, Cooper JE, Grundmann H, Robinson DA, Enright MC, Berendt T, Peacock SJ, Smith JM, Murphy M, Spratt BG: How clonal is Staphylococcus aureus?. J Bacteriol. 2003, 185 (11): 3307-3316. 10.1128/JB.185.11.3307-3316.2003.
Robinson DA, Enright MC: Evolution of Staphylococcus aureus by large chromosomal replacements. J Bacteriol. 2004, 186 (4): 1060-1064. 10.1128/JB.186.4.1060-1064.2004.
Watanabe S, Ito T, Sasaki T, Li S, Uchiyama I, Kishii K, Kikuchi K, Skov RL, Hiramatsu K: Genetic diversity of staphylocoagulase genes (coa): insight into the evolution of variable chromosomal virulence factors in Staphylococcus aureus. PLoS One. 2009, 4 (5): e5714-10.1371/journal.pone.0005714.
McAleese FM, Walsh EJ, Sieprawska M, Potempa J, Foster TJ: Loss of clumping factor B fibrinogen binding activity by Staphylococcus aureus involves cessation of transcription, shedding and cleavage by metalloprotease. J Biol Chem. 2001, 276 (32): 29969-29978. 10.1074/jbc.M102389200.
Sherertz RJ, Carruth WA, Hampton AA, Byron MP, Solomon DD: Efficacy of antibiotic-coated catheters in preventing subcutaneous Staphylococcus aureus infection in rabbits. J Infect Dis. 1993, 167 (1): 98-106.
Smyth DS, Feil EJ, Meaney WJ, Hartigan PJ, Tollersrud T, Fitzgerald JR, Enright MC, Smyth CJ: Molecular genetic typing reveals further insights into the diversity of animal-associated Staphylococcus aureus. J Med Microbiol. 2009, 58 (Pt 10): 1343-1353. 10.1099/jmm.0.009837-0.
Sambrook J, Fritsch EF, Maniatis T: Molecular Cloning: a Laboratory Manual. 1989, 2
Tamura K, Dudley J, Nei M, Kumar S: MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0. Mol Biol Evol. 2007, 24 (8): 1596-1599. 10.1093/molbev/msm092.
O'Connell DP, Nanavaty T, McDevitt D, Gurusiddappa S, Hook M, Foster TJ: The fibrinogen-binding MSCRAMM (clumping factor) of Staphylococcus aureus has a Ca2+-dependent inhibitory site. J Biol Chem. 1998, 273 (12): 6821-6829. 10.1074/jbc.273.12.6821.
Kumar S, Tamura K, Nei M: MEGA3: Integrated software for Molecular Evolutionary Genetics Analysis and sequence alignment. Brief Bioinform. 2004, 5 (2): 150-163. 10.1093/bib/5.2.150.
Takezaki N, Figueroa F, Zaleska-Rutczynska Z, Takahata N, Klein J: The phylogenetic relationship of tetrapod, coelacanth, and lungfish revealed by the sequences of forty-four nuclear genes. Mol Biol Evol. 2004, 21 (8): 1512-1524. 10.1093/molbev/msh150.
Kuroda M, Ohta T, Uchiyama I, Baba T, Yuzawa H, Kobayashi I, Cui L, Oguchi A, Aoki K, Nagai Y: Whole genome sequencing of meticillin-resistant Staphylococcus aureus. Lancet. 2001, 357 (9264): 1225-1240. 10.1016/S0140-6736(00)04403-2.
Holden MT, Feil EJ, Lindsay JA, Peacock SJ, Day NP, Enright MC, Foster TJ, Moore CE, Hurst L, Atkin R: Complete genomes of two clinical Staphylococcus aureus strains: evidence for the rapid evolution of virulence and drug resistance. Proc Natl Acad Sci USA. 2004, 101 (26): 9786-9791. 10.1073/pnas.0402521101.
We wish to acknowledge support from Trinity College Dublin for a postgraduate scholarship (for FMB). The work was supported by Grant 08/IN.1/B1845 from Science Foundation Ireland to TJF and Fondazione CARIPLO (Italy) and Fondo di Ateneo per la Ricerca (Pavia, Italy) to PS
FMB carried out cloning of fnbB genes for sequencing and protein expression, DNA and amino acid sequence analysis, fnbB DNA hybridisation experiments, phylogenetic analysis, purification of recombinant A domain proteins, ELISA experiments, SPR experiments and drafted the manuscript. NMC carried out fnbA DNA hybridization experiments involving bovine S. aureus strains. PS and SR were responsible for production of polyclonal and monoclonal antibodies against the isotype I A domain. TJF conceived and coordinated the study, and helped to draft the manuscript. All authors read and approved the final manuscript.
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Burke, F.M., McCormack, N., Rindi, S. et al. Fibronectin-binding protein B variation in Staphylococcus aureus. BMC Microbiol 10, 160 (2010). https://doi.org/10.1186/1471-2180-10-160
- Aureus Strain
- Variant Residue
- Fibronectin Binding
- Bovine Isolate