Detection of Staphylococcal Cassette Chromosome mec -Associated DNA Segments in Multiresistant Methicillin-Susceptible Staphylococcus aureus (MSSA) and Identification of Staphylococcus epidermidis ccrAB4 in both Methicillin-Resistant S. aureus and MSSA

Author:

Shore Anna C.1,Rossney Angela S.23,O'Connell Brian23,Herra Celine M.34,Sullivan Derek J.1,Humphreys Hilary56,Coleman David C.1

Affiliation:

1. Microbiology Research Unit, Division of Oral Biosciences, School of Dental Science and Dublin Dental Hospital, University of Dublin, Trinity College Dublin, Dublin 2, Ireland

2. National MRSA Reference Laboratory, St. James's Hospital, James's St., Dublin 8, Ireland

3. Department of Clinical Microbiology, University of Dublin, Trinity College Dublin, St. James's Hospital, James's St., Dublin 8, Ireland

4. School of Biological Sciences, Dublin Institute of Technology, Kevin Street, Dublin 8, Ireland

5. Department of Clinical Microbiology, Royal College of Surgeons in Ireland Education and Research Centre, Beaumont Hospital, Dublin 9, Ireland

6. Department of Microbiology, Beaumont Hospital, Dublin 9, Ireland

Abstract

ABSTRACT Methicillin-susceptible Staphylococcus aureus (MSSA) can arise from methicillin-resistant S. aureus (MRSA) following partial or complete excision of staphylococcal cassette chromosome mec (SCC mec) . This study investigated whether multiresistant MSSA isolates from Irish hospitals, where MRSA has been endemic for decades, harbor SCC mec DNA. Twenty-five multiresistant MSSA isolates recovered between 2002 and 2006 were tested for SCC mec DNA by PCR and were genotyped by multilocus sequence typing and spa typing. All isolates lacked mecA . Three isolates (12%) harbored SCC mec DNA; two of these (genotype ST8/t190) harbored a 26-kb SCC mec IID (II.3.1.2) remnant that lacked part of mecI and all of mecR1 , mecA , and IS 431 ; the third isolate (ST8/t3209) harbored the SCC mec region from dcs to orfX . All three isolates were detected as MRSA using the BD GeneOhm and Cepheid's Xpert MRSA real-time PCR assays. Six isolates (ST8/t190, n = 4; ST5/t088, n = 2), including both isolates with the SCC mec IID remnant, harbored ccrAB4 with 100% identity to ccrAB4 from the Staphylococcus epidermidis composite island SCC-CI. This ccrAB4 gene was also identified in 23 MRSA isolates representative of ST8/t190-MRSA with variant SCC mec II subtypes IIA to IIE, which predominated previously in Irish hospitals. ccrAB4 was located 5,549 bp upstream of the left SCC mec junction in both the MRSA and MSSA isolates with SCC mec elements and remnants and 5,549 bp upstream of orfX in the four MSSA isolates with ccrAB4 only on an SCC-CI homologous region. This is the first description of a large SCC mec remnant with ccr and partial mec genes in MSSA and of the S. epidermidis SCC-CI and ccrAB4 genes in S. aureus .

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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