TY - JOUR
T1 - Geographic distribution of Staphylococcus aureus causing invasive infections in Europe
T2 - A molecular-epidemiological analysis
AU - European Staphylococcal Reference Laboratory Working Group
AU - Grundmann, Hajo
AU - Aanensen, David M.
AU - Van Den Wijngaard, Cees C.
AU - Spratt, Brian G.
AU - Harmsen, Dag
AU - Friedrich, Alexander W.
AU - Sabat, Artur J.
AU - Tami, Adriana
AU - Monen, Jos
AU - Donker, Tjibbe
AU - Mittermayer, Helmut
AU - Krziwanek, Karina
AU - Stumvoll, Sabine
AU - Koller, Walter
AU - Denis, Olivier
AU - Struelens, Marc
AU - Nashev, Dimitr
AU - Budimir, Ana
AU - Kalenic, Smilja
AU - Pieridou-Bagatzouni, Despo
AU - Jakubu, Vladislav
AU - Zemlickova, Helena
AU - Westh, Henrik
AU - Sørum, Marit
AU - Skov, Robert
AU - Laurent, Frederic
AU - Ettienne, Jerome
AU - Strommenger, Birgit
AU - Witte, Wolfgang
AU - Vourli, Sofia
AU - Vatopoulos, Alkis
AU - Vainio, Anni
AU - Vuopio-Varkila, Jaana
AU - Fuzi, Miklos
AU - Ungvári, Erika
AU - Murchan, Stephan
AU - Rossney, Angela
AU - Haraldsson, Gunnsteinn
AU - Kristinsson, Karl G.
AU - Monaco, Monica
AU - Pantosti, Analisa
AU - Borg, Michael
AU - Van Santen-Verheuvel, Marga
AU - Huijsdens, Xander
AU - Marstein, Lillian
AU - Jacobsen, Trond
AU - Simonsen, Gunnar Skov
AU - Aires-de-Sousa, Marta
A2 - Miklasevics, Edvins
A2 - Balode, Arta
PY - 2010/1
Y1 - 2010/1
N2 - Background: 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. Methods and Findings: 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. Conclusions: 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.
AB - Background: 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. Methods and Findings: 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. Conclusions: 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.
KW - Staphylococcus aureus, invasive infections in EUROPE
UR - http://www.scopus.com/inward/record.url?scp=75749133613&partnerID=8YFLogxK
U2 - 10.1371/journal.pmed.1000215
DO - 10.1371/journal.pmed.1000215
M3 - Article
C2 - 20084094
AN - SCOPUS:75749133613
SN - 1549-1277
VL - 7
SP - 1
EP - 15
JO - PLoS Medicine
JF - PLoS Medicine
IS - 1
M1 - e1000215
ER -