Abstract
Methicillin-resistant Staphylococcus aureus (MRSA) with reduced vancomycin susceptibility vancomycin-intermediate S. aureus (VISA) has been reported from many countries. Whether resistance is evolving regularly in different genetic backgrounds or in a single clone with a genetic predisposition, as early results suggest, is unclear. We have studied 101 MRSA with reduced vancomycin susceptibility from nine countries by multilocus sequence typing (MLST), characterization of SCCmec (staphylococcal chromosomal cassette mec), and agr (accessory gene regulator). We found nine genotypes by MLST, with isolates within all five major hospital MRSA lineages. Most isolates (88/101) belonged to two of the earliest MRSA clones that have global prevalence. Our results show that reduced susceptibility to vancomycin has emerged in many successful epidemic lineages with no clear clonal disposition. Increasing antimicrobial resistance in genetically distinct pandemic clones may lead to MRSA infections that will become increasingly difficult to treat.
MeSH Terms
Anti-Bacterial Agents/pharmacology
Bacterial Proteins/genetics
Bacterial Typing Techniques
Drug Resistance, Bacterial/genetics
Evolution, Molecular
Humans
Methicillin Resistance
Microbial Sensitivity Tests
Sequence Analysis, DNA
Staphylococcal Infections/microbiology
Staphylococcus aureus/drug effects,genetics
Trans-Activators/genetics
Vancomycin/pharmacology
Chemicals
Agr protein, Staphylococcus aureus
Anti-Bacterial Agents
Bacterial Proteins
Trans-Activators
Vancomycin
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Howe Robin A
Southmead Hospital, Bristol, United Kingdom.
Monk Alastair
Wootton Mandy
Walsh Timothy R
Enright Mark C
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