The primers, which were designed to flank the cloning site in vector pSRP18/0 using the sequences of E. coli MG1655 [68] and pBR322 [69], were purchased from Medprobe or Biomers. Bioinformatics analysis of the cloned S. aureus sequences The sequences obtained from the insertions of the Ftp library were

compared against the genome and gene sequences of S. aureus NCTC 8325 using basic local alignment mTOR inhibitor search tool, BLASTN [27]. By accepting pairwise alignments with at least 95% sequence identity and of length at least 30 nt, a hit was recorded for 1446 and 1538 query sequences in the first and second sequence batch, respectively. All these sequences matched a single genomic region on the genome sequence. In the gene search, query sequences were required to share at least 95% identity and at least 95 nt continuous alignment against the CHIR-99021 supplier subject sequence. This search resulted in hits for 1325 and 1401 query sequences that showed a trustworthy match against 1695 and 1747 subject sequences. To have a one-to-one correspondence between queries and subjects, we only accepted the gene closest to the flag sequence end of the query sequence. Prediction

of amino acid composition and molecular mass on the basis on deduced protein sequences of the library clones was done using ProtParam-tool [70] and analyses of signal sequences were carried out using SignalP and LipoP [71, 72]. Gene sequences were also re-annotated by converting them into amino acid

sequences, performing a homology search using BLASTP [27] and choosing the most representative descriptions find more for them with Blannotator [73]. Accession numbers E. coli MG1655, GenBank: U00096 and NCBI: NC_000913; pBR322, GenBank: J01749; S. aureus subsp. aureus NCTC 8325, GenBank: CP000253 and NCBI: NC_007795; fnbA, GenBank: J04151. Acknowledgements We thank Raili Lameranta, triclocarban Heini Flinck, Sinikka Latvala, Lotta Siira, Laura Teirilä and Maiju Laaksonen for technical assistance, Lars Paulin for assistance in DNA sequencing, Patrik Koskinen for preparation of Figure 2, and Katariina Majander for valuable comments regarding the manuscript. This work was supported by the Academy of Finland (in the frame of the ERA-NET PathoGenoMics grant number 118982 and General research grant 123900) and the European Network of Excellence in EuroPathoGenomics EPG (number CEE LSHB-CT-2005-512061). Electronic supplementary material Additional file 1: “”Table S1″” shows the list of gene products found by DNA sequencing and bioinformatics of the Ftp-library. Examples of known adhesive surface proteins and adhesive polypeptides described in the current report are shown in boldface. The abbreviations used as clone and polypeptide names in the current report are shown in parenthesis. (PDF 82 KB) References 1.