Characterization of Staphylococcal Bovine Mastitis Isolates Using the Polymerase Chain Reaction

Author:

LEE SANG UN1,QUESNELL MATTHEW1,FOX LAWRENCE K.2,YOON JANG WON3,PARK YONG HO3,DAVIS WILLIAM C.4,FALK DEAN5,DEOBALD CLAUDIA F.1,BOHACH GREGORY A.1

Affiliation:

1. 1Department of Microbiology, Molecular Biology, and Biochemistry, University of Idaho, Moscow, Idaho 83844, USA

2. 2Department of Microbiology, College of Veterinary Medicine, Seoul National University, Suwon 441-744, Korea

3. 3Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, Washington 99163, USA

4. 4Department of Veterinary Clinical Medicine and Surgery, Washington State University, Pullman, Washington 99163, USA

5. 5Department of Animal and Veterinary Sciences, University ofldaho Research and Extensión Center, Twin Falls, Idaho 83303-1827, USA

Abstract

A polymerase chain reaction (PCR) assay was adapted to detect toxin genes of staphylococcal isolates from cases of bovine mastitis. Samples were obtained from three geographical areas: Korea and Idaho and Washington in the northwest United States. Samples from Korea and Washington were randomly chosen. Idaho samples were from a prospective study of mastitis etiology. Forty-one milk samples from 25 commercial farms in south-central Idaho were collected from cows with symptoms of mastitis. Although Staphylococcus aureus constituted 37.5% of mastitis isolates, these isolates lacked genes for staphylococcal enterotoxins (SEs), toxic shock syndrome toxin, and exfoliative toxins. In contrast, 4 of 13 isolates from Washington and 6 of 20 isolates from South Korea expressed SEs. These results suggest that PCR may be an effective means of screening bovine isolates for toxins. They also emphasize the potential for significant geographic differences in mastitis etiology.

Publisher

International Association for Food Protection

Subject

Microbiology,Food Science

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