Establishment and Evaluation of Real-time PCR for Food-borne Salmonella Detection
Zheng Bao-liang
Abstract
Zheng Bao-liang
Abstract
According to the inv A gene(AE008832) of Salmonella from GenBank,a pair of primers were designed to establish a real-time quantitative PCR assay.The correlation coefficient of standard curve was 0.999 and The minimal detection limit was 8 bacteria/reaction.Detecting 40 milk samples and 40 meat samples by real-time quantitative PCR,the positive rate was 2.5% and 5% respectively and the results was identical with the results by conventional microbiology method.Thus,the real-time quantitative PCR is more rapid,sensitive than other methods in detecting Salmonella,and is applicable to investigate and monitor Salmonella contamination in food.
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According to the inv A gene(AE008832) of Salmonella from GenBank,a pair of primers were designed to establish a real-time quantitative PCR assay.The correlation coefficient of standard curve was 0.999 and The minimal detection limit was 8 bacteria/reaction.Detecting 40 milk samples and 40 meat samples by real-time quantitative PCR,the positive rate was 2.5% and 5% respectively and the results was identical with the results by conventional microbiology method.Thus,the real-time quantitative PCR is more rapid,sensitive than other methods in detecting Salmonella,and is applicable to investigate and monitor Salmonella contamination in food.
Key concepts: Salmonella, Real-time polymerase chain reaction, Detection limit, GenBank, Standard curve, Contamination, Chromatography, Biology