Distribution of plasmid genes in S. aureus lineages In order to investigate the distribution of plasmid genes between S. aureus from diverse lineages we further analysed previous microarray data we generated from 254 human and animal S. aureus isolates of U.K. origin. The 198 human carriage and invasive isolates have been previously described and represent the major dominant lineages of S. aureus from hospitals and the community

[14, 21, 27]. The 55 animal isolates have previously been described and originate from cows (n = 37), horses (n = 13), sheep (n = 2), goats (n = 2) and a camel (n = 1) [28]. The array design is available in BμG@Sbase (accession number: A-BUGS-17; httpbugs.sgul.ac.uk/A-BUGS-17) Selleck Tariquidar and also ArrayExpress [28] and represents all the predicted ORFs from the first seven whole-genome S. aureus sequencing projects publically released, including five rep genes. Experiments were performed as previously reported [28]. The data used here is deposited in BμG@Sbase (accession number: E-BUGS-62 and E-BUGS-34) and also ArrayExpress (accession number: E-BUGS-62 and E-BUGS-34). Microarrays are an accurate, but not 100 % accurate, way of determining presence and absence of individual genes in individual isolates using a AZD6738 single experiment. A full discussion

of this accuracy is provided in Witney et al. [28]. Microarray heatmaps are an appropriate way to show microarray data as they accurately display the ratio of test signal and reference signal for each individual

isolate. By analyzing multiple isolates from the same lineage it is possible to determine if genes are associated with individual lineages [14, 27]. Authors’ information AJM is a Post-Doctoral Research Fellow at Hydroxychloroquine supplier St George’s, University of London interested in pathogen evolution and host-pathogen interactions of bacteria and viruses. JAL is a Reader in Microbiol Pathogenesis interested in S. aureus. Acknowledgements We are grateful to Anne Summers and Julie Shearer (University of Georgia, Athens, GA USA) for releasing plasmid sequencing data in advance of publication. We acknowledge Jason Hinds, Kate Gould, Denise Waldron and Adam Witney from the B μG@S group (the Bacterial Microarray Group at St George’s, University of London) for microarray support and The Wellcome Trust for funding the multi-collaborative microbial pathogen microarray facility under its Functional Genomics Resources Initiative. This study was supported by the PILGRIM FP7 Grant from the EU. Electronic supplementary material Additional file 1: Distribution of rep, resistance, transfer, toxin and adherence genes in sequenced plasmids. Description: Presence of rep genes in all sequenced plasmids is shown by a black box, whilst a white box indicates absence. Plasmids are classified into plasmid groups by the combination of rep sequences that they carry. The presence of resistance, transfer, toxin and adherence genes is shown by “Y”.