Emergence and Characterization of Foodborne Methicillin-Resistant Staphylococcus aureus in Korea
- Authors
- Rhee, Chae Hong; Woo, Gun-Jo
- Issue Date
- 12월-2010
- Publisher
- INT ASSOC FOOD PROTECTION
- Citation
- JOURNAL OF FOOD PROTECTION, v.73, no.12, pp.2285 - 2290
- Indexed
- SCIE
SCOPUS
- Journal Title
- JOURNAL OF FOOD PROTECTION
- Volume
- 73
- Number
- 12
- Start Page
- 2285
- End Page
- 2290
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/115195
- DOI
- 10.4315/0362-028X-73.12.2285
- ISSN
- 0362-028X
- Abstract
- A total of 165 Staphylococcus aureus strains, isolated from different food samples between 2003 and 2006, were tested for antimicrobial susceptibility. The mecA-positive methicillin-resistant S. aureus (MRSA) strains were further characterized by testing for various virulence genes and by molecular typing with multilocus sequence typing and pulsed-field gel electrophoresis. Of the 165 S. aureus isolates, 150 strains (90.9%) were resistant to at least one antibiotic while no strain was resistant to vancomycin. Four strains were resistant to both oxacillin and cefoxitin and were mecA positive. The mecA-positive MRSA strains were isolated from raw meat and fish samples (two beef samples and two fish samples) and were resistant to beta-lactam antibiotics. Based on multilocus sequence typing analysis, the isolates were assigned to sequence type 1 (ST1), ST72, and an undetermined ST (ST72 sly). All four MRSA isolates were shown to be enterotoxigenic. The ST1 MRSA isolate harbored the sea-seh gene combination and the ST72 and ST72 sly MRSA strains harbored the seg-sei and the sea-seg-sei gene combinations, respectively. However, none of the MRSA isolates had the genes for Panton-Valentine leukocidin, toxic shock syndrome toxin I, and exfoliative toxins. The pulsed-field gel electrophoresis patterns of the ST72 isolates in our study were highly similar, even though they were isolated from food samples in different years and from different regions of Korea.
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Collections - College of Life Sciences and Biotechnology > Division of Food Bioscience and Technology > 1. Journal Articles
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