2005•Journal of Clinical Laboratory ScienceRequires access

Multiplex PCR for detection of six species of foodborne pathogens

Yuliang Jiao

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Abstract

Objective To develop an effective method for detection of foodborne pathogens and diagnosis of food-poisoning.Methods Six species of foodborne pathogens,i.e.,E.coli-ETEC (Enterotoxigenic Escherichia coli) ,Bacillus cereus,Salmonella spp,E.coli-O157:H7,Shigella spp,Vibrio cholerae,were specifically detected in one multiplex PCR system.Results A method with high sensitivity and specificity was developed for the rapid detection and identification of specific pathogenic bacteria from various food materials.Conclusions The sensitivity of multiplex PCR corresponded to that of single PCR,that means both attain the same lowest detectable level of 10.30 fg.A gene diagnostic kit for food testing and diagnosis of food-poisoning will be developed by the multiplex PCR method.

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What this paper is about

Objective To develop an effective method for detection of foodborne pathogens and diagnosis of food-poisoning.Methods Six species of foodborne pathogens,i.e.,E.coli-ETEC (Enterotoxigenic Escherichia coli) ,Bacillus cereus,Salmonella spp,E.coli-O157:H7,Shigella spp,Vibrio cholerae,were specifically detected in one multiplex PCR system.Results A method with high sensitivity and specificity was developed for the rapid detection and identification of specific pathogenic bacteria from various food materials.Conclusions The sensitivity of multiplex PCR corresponded to that of single PCR,that means both attain the same lowest detectable level of 10.30 fg.A gene diagnostic kit for food testing and diagnosis of food-poisoning will be developed by the multiplex PCR method.

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Available abstract

Objective To develop an effective method for detection of foodborne pathogens and diagnosis of food-poisoning.Methods Six species of foodborne pathogens,i.e.,E.coli-ETEC (Enterotoxigenic Escherichia coli) ,Bacillus cereus,Salmonella spp,E.coli-O157:H7,Shigella spp,Vibrio cholerae,were specifically detected in one multiplex PCR system.Results A method with high sensitivity and specificity was developed for the rapid detection and identification of specific pathogenic bacteria from various food materials.Conclusions The sensitivity of multiplex PCR corresponded to that of single PCR,that means both attain the same lowest detectable level of 10.30 fg.A gene diagnostic kit for food testing and diagnosis of food-poisoning will be developed by the multiplex PCR method.

Key concepts: Bacillus cereus, Multiplex polymerase chain reaction, Vibrio cholerae, Salmonella, Microbiology, Biology, Shigella, Multiplex

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