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1 Department of Microbiology, Moyne Institute of Preventive Medicine, Trinity College Dublin, University of Dublin, Dublin 2, Republic of Ireland
2 Microbiology Research Unit, Division of Oral Biosciences, Dublin Dental School and Hospital, Trinity College Dublin, University of Dublin, Dublin 2, Republic of Ireland
Correspondence
Cyril J. Smyth
csmyth{at}tcd.ie
Received 30 October 2007
Accepted 27 November 2007
ent1 and
ent2 and 19 having the selu gene. The seh and sell genes, the selk–selq gene combination, and the tst gene were each found in <15 % of isolates. The agr genotype distribution was agr type III, 37.5 %; agr type I, 35.4 %; agr type II, 25 %; and agr type IV, 2.1 %. There was no association between SE–SEl genotype and agr type. All tst gene-positive isolates were of agr type III and harboured a classical SE gene. Multiple locus, variable number tandem repeat analysis (MLVA) produced 47 different patterns. While the sdr locus was present in all isolates, half of them lacked one or two of the sdr gene amplimers. Twenty isolates harboured the bbp gene, its presence being associated with agr type III, but not with the SE–SEl gene profile. The agr types of isolates were associated with MLVA subclusters. Selective MLST analysis revealed seven novel sequence types and a new aroE allele. Five clonal clusters (CCs), including CCs comprising major pandemic clones CC30, CC5 and CC22 and minor lineages CC6 and CC9, and three singletons were identified.
Abbreviations: CC, clonal cluster; MLVA, multiple locus, variable number tandem repeat analysis; PFGE, pulsed-field gel electrophoresis; SE, staphylococcal enterotoxin; SEl, staphylococcal enterotoxin-like; slv, single locus variant; ST, sequence type; TSST-1, toxic shock syndrome toxin-1.
Present address: New York Medical College, Department of Microbiology and Immunology, Valhalla, NY 10595, USA.
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