Juhsien J C Nienaber,
Batu K Sharma Kuinkel,
Michael Clarke-Pearson,
Supaporn Lamlertthon,
Lawrence Park,
Thomas H Rude,
Steve Barriere,
Christopher W Woods,
Vivian H Chu,
Mercedes Marín,
Suzana Bukovski, Patricia Garcia,
G Ralph Corey,
Tony Korman,
Thanh Doco-Lecompte,
David R Murdoch,
L Barth Reller,
Vance G Fowler
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ABSTRACT: Using multinational collections of methicillin-susceptible Staphylococcus aureus (MSSA) isolates from infective endocarditis (IE) and soft tissue infections (STIs), we sought to (1) validate the finding that S. aureus in clonal complex (CC) 30 is associated with hematogenous complications and (2) test the hypothesis that specific genetic characteristics in S. aureus are associated with infection severity.
IE and STI isolates from 2 cohorts were frequency matched by geographic origin. Isolates underwent spa typing to infer CC and multiplex polymerase chain reaction for presence of virulence genes.
114 isolate pairs were genotyped. IE isolates were more likely to be CC30 (19.5% vs 6.2%; P = .005) and to contain 3 adhesins (clfB, cna, map/eap; P < .0001 for all) and 5 enterotoxins (tst, sea, sed, see, and sei; P ≤ .005 for all). CC30 isolates were more likely to contain cna, tst, sea, see, seg, and chp (P < .05 for all).
MSSA IE isolates were significantly more likely to be CC30 and to possess a distinct repertoire of virulence genes than MSSA STI isolates from the same region. The genetic basis of this association requires further study.
The Journal of Infectious Diseases 09/2011; 204(5):704-13. · 6.41 Impact Factor
