Author:
Kinnevey Peter M.,Shore Anna C.,Brennan Grainne I.,Sullivan Derek J.,Ehricht Ralf,Monecke Stefan,Slickers Peter,Coleman David C.
Abstract
ABSTRACTMethicillin-resistantStaphylococcus aureus(MRSA) has been a major cause of nosocomial infection in Irish hospitals for 4 decades, and replacement of predominant MRSA clones has occurred several times. An MRSA isolate recovered in 2006 as part of a larger study of sporadic MRSA exhibited a rarespa(t878) and multilocus sequence (ST779) type and was nontypeable by PCR- and DNA microarray-based staphylococcal cassette chromosomemec(SCCmec) element typing. Whole-genome sequencing revealed the presence of a novel 51-kb composite island (CI) element with three distinct domains, each flanked by direct repeat and inverted repeat sequences, including (i) a pseudo SCCmecelement (16.3 kb) carryingmecAwith a novelmecclass region, a fusidic acid resistance gene (fusC), and two copper resistance genes (copBandcopC) but lackingccrgenes; (ii) an SCC element (17.5 kb) carrying a novelccrAB4allele; and (iii) an SCC element (17.4 kb) carrying a novelccrCallele and a clustered regularly interspaced short palindromic repeat (CRISPR) region. The novel CI was subsequently identified by PCR in an additional 13 t878/ST779 MRSA isolates, six from bloodstream infections, recovered between 2006 and 2011 in 11 hospitals. Analysis of open reading frames (ORFs) carried by the CI showed amino acid sequence similarity of 44 to 100% to ORFs fromS. aureusand coagulase-negative staphylococci (CoNS). These findings provide further evidence of genetic transfer betweenS. aureusand CoNS and show how this contributes to the emergence of novel SCCmecelements and MRSA strains. Ongoing surveillance of this MRSA strain is warranted and will require updating of currently used SCCmectyping methods.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
61 articles.
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