Geographic distribution of Staphylococcus aureus causing invasive infections in Europe: a molecular-epidemiological analysis
Staphylococcus aureus is one of the most important human pathogens and methicillin-resistant variants (MRSAs) are a major cause of hospital and community-acquired infection. We aimed to map the geographic distribution of the dominant clones that cause invasive infections in Europe. In each country,...
Saved in:
Published in: | PLoS medicine Vol. 7; no. 1; p. e1000215 |
---|---|
Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
Public Library of Science
01-01-2010
Public Library of Science (PLoS) |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Staphylococcus aureus is one of the most important human pathogens and methicillin-resistant variants (MRSAs) are a major cause of hospital and community-acquired infection. We aimed to map the geographic distribution of the dominant clones that cause invasive infections in Europe.
In each country, staphylococcal reference laboratories secured the participation of a sufficient number of hospital laboratories to achieve national geo-demographic representation. Participating laboratories collected successive methicillin-susceptible (MSSA) and MRSA isolates from patients with invasive S. aureus infection using an agreed protocol. All isolates were sent to the respective national reference laboratories and characterised by quality-controlled sequence typing of the variable region of the staphylococcal spa gene (spa typing), and data were uploaded to a central database. Relevant genetic and phenotypic information was assembled for interactive interrogation by a purpose-built Web-based mapping application. Between September 2006 and February 2007, 357 laboratories serving 450 hospitals in 26 countries collected 2,890 MSSA and MRSA isolates from patients with invasive S. aureus infection. A wide geographical distribution of spa types was found with some prevalent in all European countries. MSSA were more diverse than MRSA. Genetic diversity of MRSA differed considerably between countries with dominant MRSA spa types forming distinctive geographical clusters. We provide evidence that a network approach consisting of decentralised typing and visualisation of aggregated data using an interactive mapping tool can provide important information on the dynamics of MRSA populations such as early signalling of emerging strains, cross border spread, and importation by travel.
In contrast to MSSA, MRSA spa types have a predominantly regional distribution in Europe. This finding is indicative of the selection and spread of a limited number of clones within health care networks, suggesting that control efforts aimed at interrupting the spread within and between health care institutions may not only be feasible but ultimately successful and should therefore be strongly encouraged. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Membership of the European Staphylococcal Reference Laboratory Working Group is provided in the Acknowledgments. ICMJE criteria for authorship read and met: HG DMA CCvdW BGS DH AWF. Agree with the manuscript's results and conclusions: HG DMA CCvdW BGS DH AWF. Designed the experiments/the study: HG DH. Analyzed the data: HG CCvdW BGS AWF. Collected data/did experiments for the study: HG. Wrote the first draft of the paper: HG. Contributed to the writing of the paper: HG CCvdW BGS DH AWF. Developed the public domain Web-based interactive mapping tool: DMA. Carried out spatial scan statistics: CCvdW. Provided scientific advice, co-developed mapping tools, co-edited manuscript: BGS. Developed the SpaTyper software, co-organised the capacity building workshops, maintained and serviced the SpaServer: DH. Maintained the SeqNet.org database, co-organised the capacity building workshops, responsible for proficiency testing, performed BURP-clustering: AWF. |
ISSN: | 1549-1676 1549-1277 1549-1676 |
DOI: | 10.1371/journal.pmed.1000215 |