Molecular epidemiology of community-onset methicillin-resistant Staphylococcus aureus infections in Israel

A. Biber, M. Parizade, D. Taran, H. Jaber, E. Berla, C. Rubin, G. Rahav, D. Glikman, G. Regev-Yochay

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

Data on community-associated (CA) methicillin-resistant Staphylococcus aureus (MRSA) in Israel are scarce. The objective of this study was to characterize the major CA-MRSA clones in Israel. All clinical MRSA isolates detected in the community during a period of 2.5 years (2011–2013) from individuals insured by a major health maintenance organization in Israel were collected, with additional data from medical records. Antibiotic susceptibility patterns and staphylococcal chromosomal cassette mec (SCCmec) typing were determined. SCCmec IV and V isolates were further typed by pulsed-field gel electrophoresis (PFGE), spa typing, and detection of a panel of toxin genes. MRSA were detected in 280 patients, mostly from skin infections. Patients with SCCmec IV (n = 120, 43 %) were younger (p < 0.0001) and reported less contact with healthcare facilities. Almost all isolates were trimethoprim–sulfamethoxazole susceptible (98 %). spa-CC032, a typical nosocomial MRSA clone, accounted for 28 % of SCCmec IV. The two major CA-MRSA clones were t008 USA300 (13 %) and t991 (10 %); t991 was isolated mainly from children (75 %), was Panton–Valentine leukocidin (PVL) negative but eta-positive, and was typically susceptible to most antibiotic groups. PVL-positive strains (n = 31) included mainly USA300 (52 %) and t019 (13 %). While multiple genetic lineages were evident among community-onset MRSA in Israel, approximately 20 % are typical CA-MRSA clones, mainly USA300 and a local clone, t991.

Original languageEnglish
Pages (from-to)1603-1613
Number of pages11
JournalEuropean Journal of Clinical Microbiology and Infectious Diseases
Volume34
Issue number8
DOIs
StatePublished - 27 Aug 2015

Bibliographical note

Publisher Copyright:
© 2015, Springer-Verlag Berlin Heidelberg.

Funding

This study was supported by grant number 3-7599 from the Chief Scientist Office of the Ministry of Health, Israel.

FundersFunder number
Ministry of Health, State of Israel

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