Experiments are currently underway to examine the biological sign

Experiments are currently underway to examine the biological significance of fibronectin-selleck screening library 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. Conclusions 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 PF-3084014 cell line 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. HDAC inhibitors list These data have implications for the FnBPB A domain as a target for a vaccine or immunotherapeutics. Methods 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). Ribonuclease T1 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) [27]. Strain P1 is a rabbit virulent strain [31] and has been characterised by MLST [22]. 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 [32]. Table 2 S. aureus strains screened for FnBPB isotypes.

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