Application of groEL gene for the species-specific detection of Vibrio parahaemolyticus by PCR

被引:23
作者
Hossain, M. T. [1 ]
Kim, E. -Y. [1 ]
Kim, Y. -R. [1 ]
Kim, D. -G. [2 ]
Kong, I. -S. [1 ]
机构
[1] Pukyong Natl Univ, Dept Biotechnol, Pusan 608737, South Korea
[2] Natl Fisheries Res & Dev Inst, Biotechnol Res Div, Pusan, South Korea
关键词
groEL gene; PCR; shellfish; species-specific; Vibrio parahaemolyticus;
D O I
10.1111/j.1472-765X.2011.03174.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aims: Vibrio parahaemolyticus is a significant cause of human gastrointestinal disorders and is transmitted through ingestion of raw or undercooked contaminated seafood. We used the groEL gene for the species-specific detection of V.parahaemolyticus from artificially inoculated shellfish, fish and seawater. Methods and Results: The nucleotide sequences of 24 Vibrio and seven nonVihrio spp. were compared, and less conserved regions were selected for the designing of primer sets. To detect V parfthaemo/yticus specifically, PCR conditions were standardized and tested to evaluate the specificity of primers. A 510-bp band was appeared only from V. parahacmolyticus by PCR. Notably, the detection was shown to be functional at high annealing temperature above 68 C. The groEL primers detected 100 pg and 1 ng of DNA purified from V. paralloemolyticus culture and artificially infected oyster tissue, respectively. Conclusions: The graEL gene is a potential marker for the species-specific detection of V parohaemolyticus and could be used to detect this bacterium in contaminated food by PCR. Significance and Impact of the Study: PCR using primers designed from groEE gene provide an efficient method for the accurate identification of V puraluiemolyticus from contaminated samples.
引用
收藏
页码:67 / 72
页数:6
相关论文
共 15 条
[1]  
Ausubel F.M., 1998, CURRENT PROTOCOLS MO
[2]   Lactobacillus strain diversity based on partial hsp60 gene sequences and design of PCR-restriction fragment length polymorphism assays for species identification and differentiation [J].
Blaiotta, Giuseppe ;
Fusco, Vincenzina ;
Ercolini, Danilo ;
Aponte, Maria ;
Pepe, Olimpia ;
Villani, Francesco .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2008, 74 (01) :208-215
[3]   Microarray analysis of microbial virulence factors [J].
Chizhikov, V ;
Rasooly, A ;
Chumakov, K ;
Levy, DD .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2001, 67 (07) :3258-3263
[4]   Comparison of different biochemical and molecular methods for the identification of Vibrio parahaemolyticus [J].
Croci, L. ;
Suffredini, E. ;
Cozzi, L. ;
Toti, L. ;
Ottaviani, D. ;
Pruzzo, C. ;
Serratore, P. ;
Fischetti, R. ;
Goffredo, E. ;
Loffredo, G. ;
Mioni, R. .
JOURNAL OF APPLIED MICROBIOLOGY, 2007, 102 (01) :229-237
[5]  
Hecker KH, 1996, BIOTECHNIQUES, V20, P478
[6]  
Hu YS, 2010, AFR J MICROBIOL RES, V4, P1733
[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]   Isolation of the groESL cluster from Vibrio anguillarum and PCR detection targeting groEL gene [J].
Kim, Dong-Gyun ;
Kim, Yu-Ri ;
Kim, Eun-Young ;
Cho, Hyun Min ;
Ahn, Sun-Hee ;
Kong, In-Soo .
FISHERIES SCIENCE, 2010, 76 (05) :803-810
[9]   Application of the rpoS Gene for Species-Specific Detection of Vibrio vulnificus by Real-Time PCR [J].
Kim, Dong-Gyun ;
Ahn, Sun-Hee ;
Kim, Lyoung-Hwa ;
Park, Kee-Jai ;
Hong, Yong-Ki ;
Kong, In-Soo .
JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, 2008, 18 (11) :1841-1847
[10]  
Nishibuchi M., 2006, MOL IDENTIFICATION, P44