Abstract

BackgroundSeveral 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 FindingsA 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.ConclusionsOur results imply that CA-MRSA origin, epidemiology and population structure in Europe is very dissimilar from that of USA.

Highlights

  • Staphylococcus aureus, methicillin-resistant S. aureus (MRSA) is one of the most important nosocomial pathogens

  • Our results imply that community-associated MRSA (CA-MRSA) origin, epidemiology and population structure in Europe is very dissimilar from that of USA

  • Molecular typing studies showed that CA-MRSA differs from hospital-associated MRSA (HA-MRSA) [9]: they belong to distinct genetic lineages, usually carry smaller staphylococcal cassette chromosome mec (SCCmec) cassettes and specific virulence factors, such as PVL (Panton-Valentine leukocidin) and arginine catabolic mobile element (ACME)

Read more

Summary

Introduction

Staphylococcus aureus, methicillin-resistant S. aureus (MRSA) is one of the most important nosocomial pathogens. Resistance to methicillin is conferred by the mecA gene, which is carried within a mobile genetic element called staphylococcal cassette chromosome mec (SCCmec) [1]. MRSA was confined to hospitals, but in the early 1990s, infections in healthy individuals emerged among Aborigines’ communities in Australia [6]. Molecular typing studies showed that CA-MRSA differs from hospital-associated MRSA (HA-MRSA) [9]: they belong to distinct genetic lineages, usually carry smaller SCCmec cassettes and specific virulence factors, such as PVL (Panton-Valentine leukocidin) and ACME (arginine catabolic mobile element). Several studies have addressed the epidemiology of community-associated Staphylococcus aureus (CA-SA) in Europe; a comprehensive perspective remains unclear. 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

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call