PLoS ONE · 2011 · 16 citations · 25 references
Life SciencesGeneticsMicrobiologyComparative GenomicsGenomicsMicrobial GeneticsBacterial InfectionsComparative Genomic HybridizationComparative Microbial GenomicsMicrobial DiversificationMicrobial Evolutionary GenomicsPathogen GenomicsClusteringCommunity-acquired Methicillin-resistant Staphylococcus Aureus InfectionComparative Pathogen GenomicsGenomic Characterization Of PathogensGenomic ClusteringGenotypic Characterization Of IsolatesLineage AssignmentSingle-nucleotide Polymorphisms
INTRODUCTION: Community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) are increasingly isolated, with USA300-0114 being the predominant clone in the USA. Comparative whole genome sequencing of USA300 isolates collected in 2002, 2003 and 2005 showed a limited number of single nucleotide polymorphisms and regions of difference. This suggests that USA300 has undergone rapid clonal expansion without great genomic diversification. However, whole genome comparison of CA-MRSA has been limited to isolates belonging to USA300. The aim of this study was to compare the genetic repertoire of different CA-MRSA clones with that of HA-MRSA from the USA and Europe through comparative genomic hybridization (CGH) to identify genetic clues that may explain the successful and rapid emergence of CA-MRSA. MATERIALS AND METHODS: Hierarchical clustering based on CGH of 48 MRSA isolates from the community and nosocomial infections from Europe and the USA revealed dispersed clustering of the 19 CA-MRSA isolates. This means that these 19 CA-MRSA isolates do not share a unique genetic make-up. Only the PVL genes were commonly present in all CA-MRSA isolates. However, 10 genes were variably present among 14 USA300 isolates. Most of these genes were present on mobile elements. CONCLUSION: The genetic variation present among the 14 USA300 isolates is remarkable considering the fact that the isolates were recovered within one month and originated from a confined geographic area, suggesting continuous evolution of this clone.
25
Mark C. Enright, Nicholas Day, Catrin E. Davies et al. · Journal of Clinical Microbiology · 2000 · 3K citations · Full text
Dag Harmsen, Heike Claus, Wolfgang Witte et al. · Journal of Clinical Microbiology · 2003 · 1.6K citations · Full text
Linda K. McDougal, Christine D. Steward, George Killgore et al. · Journal of Clinical Microbiology · 2003 · 1.4K citations · Full text