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Multiplex real-time PCR assay for detection of pathogenic Vibrio parahaemolyticus strains
Institution:1. Department of Biological Engineering, Inha University, Incheon, Republic of Korea;2. West sea Fisheries Institute, National Institute of Fisheries Sciencet (NIFS), Incheon, Republic of Korea;3. Food Safety and Processing Research Division, National Institute of Fisheries Science (NIFS), Busan, Republic of Korea;1. Food Safety Testing Center, Beijing Entry–Exit Inspection and Quarantine Bureau of the People''s Republic of China, Beijing 100026, China;2. National Center for Nanoscience and Technology, Beijing 100190, China;3. Beijing University of Agriculture, Beijing 102206, China
Abstract:Foodborne disease caused by pathogenic Vibrio parahaemolyticus has become a serious public health problem in many countries. Rapid diagnosis and the identification of pathogenic V. parahaemolyticus are very important in the context of public health. In this study, an EvaGreen-based multiplex real-time PCR assay was established for the detection of pathogenic V. parahaemolyticus. This assay targeted three genetic markers of V. parahaemolyticus (species-specific gene toxR and virulence genes tdh and trh). The assay could unambiguously identify pathogenic V. parahaemolyticus with a minimum detection limit of 1.4 pg genomic DNA per reaction (concentration giving a positive multiplex real-time PCR result in 95% of samples). The specificity of the assay was evaluated using 72 strains of V. parahaemolyticus and other bacteria. A validation of the assay with clinical samples confirmed its sensitivity and specificity. Our data suggest the newly established multiplex real-time PCR assay is practical, cost-effective, specific, sensitive and capable of high-throughput detection of pathogenic V. parahaemolyticus.
Keywords:Multiplex real-time PCR
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