Multiplex real-time PCR assay for detection of pathogenic Vibrio parahaemolyticus strains

被引:29
作者
He, Peiyan [1 ]
Chen, Zhongwen [1 ]
Luo, Jianyong [1 ]
Wang, Henghui [1 ]
Yan, Yong [1 ]
Chen, Lixia [1 ]
Gao, Wenjie [1 ]
机构
[1] Jiaxing Ctr Dis Control & Prevent, Jiaxing 314050, Zhejiang, Peoples R China
关键词
Vibrio parahaemolyticus; Multiplex real-time PCR; toxR; tdh; trh; POLYMERASE-CHAIN-REACTION; SEAFOOD; DIFFERENTIATION; JAPAN; SEA;
D O I
10.1016/j.mcp.2014.06.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2014 Published by Elsevier Ltd.
引用
收藏
页码:246 / 250
页数:5
相关论文
共 21 条
[1]  
Alam MJ, 2002, FEMS MICROBIOL LETT, V208, P83
[2]   Development and evaluation of a multiplex PCR for simultaneous detection of five foodborne pathogens [J].
Chen, J. ;
Tang, J. ;
Liu, J. ;
Cai, Z. ;
Bai, X. .
JOURNAL OF APPLIED MICROBIOLOGY, 2012, 112 (04) :823-830
[3]   Development of melting temperature-based SYBR Green I polymerase chain reaction methods for multiplex genetically modified organism detection [J].
Hernández, M ;
Rodríguez-Lázaro, D ;
Esteve, T ;
Prat, S ;
Pla, M .
ANALYTICAL BIOCHEMISTRY, 2003, 323 (02) :164-170
[4]  
Honda T., 1993, Reviews in Medical Microbiology, V4, P106, DOI [DOI 10.1097/00013542-199304000-00006, 10.1097/00013542-199304000-00006]
[5]   Multiplex PCR for the detection and differentiation of Vibrio parahaemolyticus strains using the groEL, tdh and trh genes [J].
Hossain, Muhammad Tofazzal ;
Kim, Young-Ok ;
Kong, In-Soo .
MOLECULAR AND CELLULAR PROBES, 2013, 27 (5-6) :171-175
[6]  
Huang J, 2009, APPL ENVIRON MICROB, V75, P6981
[7]   Epidemiology of Seafood-Associated Infections in the United States [J].
Iwamoto, Martha ;
Ayers, Tracy ;
Mahon, Barbara E. ;
Swerdlow, David L. .
CLINICAL MICROBIOLOGY REVIEWS, 2010, 23 (02) :399-+
[8]   Presence of pathogenic Vibrio Parahaemolyticus in waters and seafood from the Tunisian Sea [J].
Khouadja, Sadok ;
Suffredini, Elisabetta ;
Spagnoletti, Matteo ;
Croci, Luciana ;
Colombo, Mauro M. ;
Amina, Bakhrouf .
WORLD JOURNAL OF MICROBIOLOGY & BIOTECHNOLOGY, 2013, 29 (08) :1341-1348
[9]   The development of rapid real-time PCR detection system for Vibrio parahaemolyticus in raw oyster [J].
Kim, J. S. ;
Lee, G. G. ;
Kim, J. ;
Kwon, J. Y. ;
Kwon, S. -T. .
LETTERS IN APPLIED MICROBIOLOGY, 2008, 46 (06) :649-654
[10]  
Lipsky RH, 2001, CLIN CHEM, V47, P635