4.6 Article

High Genetic Diversity among Community-Associated Staphylococcus aureus in Europe: Results from a Multicenter Study

期刊

PLOS ONE
卷 7, 期 4, 页码 -

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PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0034768

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资金

  1. European Commission [CONCORD-HEALTH-F3-2008-222718]
  2. Fundacao para a Ciencia e Tecnologia (FCT), Portugal [SFRH/BD/72675/2010, SFRH/BPD/66514/2009, SFRH/BD/44220/2008]
  3. Ministry of Science and Higher Education, Poland [1216/7. PR UE/2009/7]
  4. FCT [Pest-OE/EQB/LAO004/2011]
  5. Internal Grant Agency, Ministry of Health [IGA9642-4, IGA NT12395-5/2011]
  6. Hungarian National Scientific Research Fund [OTKA T 46186]
  7. Fundação para a Ciência e a Tecnologia [SFRH/BD/44220/2008, SFRH/BPD/66514/2009] Funding Source: FCT

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Background: Several studies have addressed the epidemiology of community-associated Staphylococcus aureus (CA-SA) in Europe; nonetheless, a comprehensive perspective remains unclear. In this study, we aimed to describe the population structure of CA-SA and to shed light on the origin of methicillin-resistant S. aureus (MRSA) in this continent. Methods and Findings: A total of 568 colonization and infection isolates, comprising both MRSA and methicillin-susceptible S. aureus (MSSA), were recovered in 16 European countries, from community and community-onset infections. The genetic background of isolates was characterized by molecular typing techniques (spa typing, pulsed-field gel electrophoresis and multilocus sequence typing) and the presence of PVL and ACME was tested by PCR. MRSA were further characterized by SCCmec typing. We found that 59% of all isolates were associated with community-associated clones. Most MRSA were related with USA300 (ST8-IVa and variants) (40%), followed by the European clone (ST80-IVc and derivatives) (28%) and the Taiwan clone (ST59-IVa and related clonal types) (15%). A total of 83% of MRSA carried Panton-Valentine leukocidin (PVL) and 14% carried the arginine catabolic mobile element (ACME). Surprisingly, we found a high genetic diversity among MRSA clonal types (ST-SCCmec), Simpson's index of diversity = 0.852 (0.788-0.916). Specifically, about half of the isolates carried novel associations between genetic background and SCCmec. Analysis by BURP showed that some CA-MSSA and CA-MRSA isolates were highly related, suggesting a probable local acquisition/loss of SCCmec. Conclusions: Our results imply that CA-MRSA origin, epidemiology and population structure in Europe is very dissimilar from that of USA.

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