High Heterogeneity within Methicillin-Resistant Staphylococcus aureus ST398 Isolates, Defined by Cfr9I Macrorestriction-Pulsed-Field Gel Electrophoresis Profiles and spa and SCC mec Types

Author:

Argudín M. A.12,Fetsch A.2,Tenhagen B.-A.2,Hammerl J. A.2,Hertwig S.2,Kowall J.2,Rodicio M. R.1,Käsbohrer A.2,Helmuth R.2,Schroeter A.2,Mendoza M. C.1,Bräunig J.2,Appel B.2,Guerra B.2

Affiliation:

1. Departmento de Biología Funcional (Área de Microbiología) and Instituto Universitario de Biotecnología, University of Oviedo, Julían Clavería 6, E-33006 Oviedo, Spain

2. Department of Biological Safety, Federal Institute for Risk Assessment (BfR), Diedersdorfer Weg 1, D-12277 Berlin, Germany

Abstract

ABSTRACT During recent years, the animal-associated methicillin-resistant Staphylococcus aureus clone ST398 has extensively been studied. The DNA of these isolates turned out to be refractory to SmaI restriction, and consequently, SmaI is unsuitable for subtyping this clone by standard pulsed-field gel electrophoresis (PFGE). Very recently, ST398 DNA was shown to be digested by Cfr9I, a neoschizomer of SmaI. In the present study, we employed Cfr9I PFGE on 100 German and 5 Dutch ST398 isolates and compared their PFGE profiles, protein A gene variable repeat regions ( spa types), and types of the staphylococcal cassette chromosome mec (SCC mec ). The isolates (from healthy carrier pigs, clinical samples from pigs, dust from farms, milk, and meat) were assigned to 35 profiles, which were correlated to the SCC mec type. A dendrogram with the Cfr9I patterns assigned all profiles to two clusters. Cluster A grouped nearly all isolates with SCC mec type V, and cluster B comprised all SCC mec type IVa and V* (a type V variant first identified as III) carriers plus one isolate with SCC mec type V. Both clusters also grouped methicillin-susceptible S. aureus isolates. The association of the majority of isolates with SCC mec type V in one large cluster indicated the presence of a successful subclone within the clonal complex CC398 from pigs, which has diversified. In general, the combination of Cfr9I PFGE with spa and SCC mec typing demonstrated the heterogeneity of the series analyzed and can be further used for outbreak investigations and traceability studies of the MRSA ST398 emerging clone.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference40 articles.

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3. Argudín, M. A., M. R. Rodicio, and B. Guerra. 2009. The emerging methicillin-resistant Staphylococcus aureus ST398 clone can easily be typed using Cfr9I SmaI neoschizomer. Lett. Appl. Microbiol.50:127-130.

4. Presence of a Novel DNA Methylation Enzyme in Methicillin-Resistant Staphylococcus aureus Isolates Associated with Pig Farming Leads to Uninterpretable Results in Standard Pulsed-Field Gel Electrophoresis Analysis

5. Bhat, M., C. Dumortier, B. S. Taylor, M. Miller, G. Vasquez, J. Yunen, K. Brudney, E. J. Sánchez, C. Rodriguez-Taveras, R. Rojas, P. Leon, and F. D. Lowy. 2009. Staphylococcus aureus ST398, New York City and Dominican Republic. Emerg. Infect. Dis.15:285-287.

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