Potential Associations between Severity of Infection and the Presence of Virulence-Associated Genes in Clinical Strains of Staphylococcus aureus
Author(s) -
Steven R. Gill,
Lauren M. McIntyre,
Charlotte Nelson,
Brian G. Remortel,
Tom H. Rude,
L. Barth Reller,
Vance G. Fowler
Publication year - 2011
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0018673
Subject(s) - sccmec , staphylococcus aureus , virulence , microbiology and biotechnology , biology , staphylococcal infections , gene , methicillin resistant staphylococcus aureus , genetics , bacteria
Background The clinical spectrum of Staphylococcus aureus infection ranges from asymptomatic nasal carriage to osteomyelitis, infective endocarditis (IE) and death. In this study, we evaluate potential association between the presence of specific genes in a collection of prospectively characterized S. aureus clinical isolates and clinical outcome. Methodology/Principal Findings Two hundred thirty-nine S. aureus isolates (121 methicillin-resistant S. aureus [MRSA] and 118 methicillin-susceptible S. aureus [MSSA]) were screened by array comparative genomic hybridization (aCGH) to identify genes implicated in complicated infections. After adjustment for multiple tests, 226 genes were significantly associated with severity of infection. Of these 226 genes, 185 were not in the SCC mec element. Within the 185 non-SCC mec genes, 171 were less common and 14 more common in the complicated infection group. Among the 41 genes in the SCC mec element, 37 were more common and 4 were less common in the complicated group. A total of 51 of the 2014 sequences evaluated, 14 non-SCC mec and 37 SCC mec , were identified as genes of interest. Conclusions/Significance Of the 171 genes less common in complicated infections, 152 are of unknown function and may contribute to attenuation of virulence. The 14 non-SCC mec genes more common in complicated infections include bacteriophage-encoded genes such as regulatory factors and autolysins with potential roles in tissue adhesion or biofilm formation.
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