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Genotypic Classification of Staphylococcus aureus and Bacillus cereus from Korean Slaughterhouses Using Semiautomated Repetitive Sequence-Based Polymerase Chain Reaction

Authors
Han, Sang-HaKim, Jong-HuiNa, JeongkyeongYoo, Jae GyuOh, Mi-Hwa
Issue Date
Nov-2019
Publisher
MARY ANN LIEBERT, INC
Keywords
foodborne pathogen; genotypes; identification; rep-PCR
Citation
FOODBORNE PATHOGENS AND DISEASE, v.16, no.11, pp 769 - 777
Pages
9
Journal Title
FOODBORNE PATHOGENS AND DISEASE
Volume
16
Number
11
Start Page
769
End Page
777
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/44614
DOI
10.1089/fpd.2019.2619
ISSN
1535-3141
1556-7125
Abstract
A repetitive sequence-based polymerase chain reaction (rep-PCR) technique utilizing a semiautomated system, namely DiversiLab, was applied to determine the genotypes of Staphylococcus aureus and Bacillus cereus obtained from slaughterhouses. Twenty-four S. aureus and 16 B. cereus isolates from pigs and Hanwoo cattle from three slaughterhouses were used to create a DNA fingerprint library with the system software. Scatterplots demonstrated that rep-PCR groupings of S. aureus isolates were in good agreement with their origins. Specifically, linked rep-PCR profiles were observed for S. aureus isolates recovered from the same slaughterhouse, and higher genetic similarities were found among strains isolated from adjacent regions. All S. aureus isolates except one (ID: A-Hanwoo-9) from slaughterhouse "A" clustered with the three S. aureus reference strains, Korea Culture Center of Microorganisms (KCCM) 41291, KCCM 12214, and Culture Collection of Antimicrobial Resistant Microbes (CCARM) 3A007 (similarity values >95%). Moreover, most isolates obtained from slaughterhouse "B" clustered with S. aureus KCCM 11335 and KCCM 41331, and two isolates from slaughterhouse "C" clustered with CCARM 0027. Therefore, for this species, genotypic characteristics of regional isolates can be used to track the pathway of contamination. In contrast, B. cereus isolates showed high genetic diversity and could not be clustered with any specific group. Collectively, this system is useful for analyzing genetic diversity and is a rapid and reproducible typing method; however, there is a need to develop rep-PCR libraries for its use as a rapid identification method.
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