J4 ›› 2012, Vol. 38 ›› Issue (2): 382-385.

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Evaluation on detection efficacy of multiplex PCR method |of several enteric pathogens

LIU Jin-hua1,SHI Yan-yu2,MA Lu-yao3,WEI Chun-yan1,SHAO Li-jun1,WANG Hai-long4,5   

  1. 1. Jilin Entry-Exit Inspection and Quarantine Bureau,Changchun 130062,China;2. Jilin Product Quality Supervision Inspection Institute,Changchun 130022,China;3.Departemt of Biomedical Engineering, School of Pharmacy,Jilin University,Changchun 130021,China;4. Xilin Gol League,Inner Mongolia Public Security Bureau in East Ujimqinqi,Wuliyasitai Town 026300,China;5.Institute of Frontier  |Medicine |Science,Jilin University,Changchun 130021,China
  • Received:2011-10-28 Online:2012-03-28 Published:2012-03-28

Abstract:

Abstract:Objective To  establish a rapid accurate method to detect four kinds of enteric pathogens including Listeria monocytogenes,Escherichia coli O157,Proteusbacillus vulgaris,Vibiro parahaemolyticus with multiplex PCR.Methods The special primers were designed of these bacteria for multiplex PCR respectively.Using this screening system to detect the commercially available juice which had been artificially randomly contaminated.Results Multiplex PCR could effectively amplify the corresponding gene fragments,the amlification fragments of Listeria monocytogene,Eschericha coli O157,Proteusbacillus vulgaris and Vibiro parahaemolyticus were 155,366,522 and 199 bp.The sensitivity of the pathogens  reached 103CFU/mL;as a result,any of three kinds of bacteria randomly contaminated in the juice could be identified successfully.Conclusion The use of multiplex PCR make it possible that whether the food is carrying the  four pathogenic bacteria mentioned above.

Key words: multiplex polymerase chain reaction;Escherichia coli O157;Proteusbacillus vulgaris;Vibiro parahaemolyticus;Listeria monocytogenes;

CLC Number: 

  • R515