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A new real-time PCR assay for the specific detection of Salmonella spp. targeting the bipA gene.

机译:一种用于特异性检测沙门氏菌的新型实时荧光定量PCR检测方法。靶向bipA基因。

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A straightforward real-time polymerase chain reaction (PCR)-based assay was designed and evaluated for the detection of Salmonella spp. in food and water samples. This new assay is based on the specific detection of the bipA gene of Salmonella, which encodes a protein of the guanosine triphosphate (GTP)-binding elongation family that displays global modulating properties, by regulating a wide variety of downstream processes. The new method correctly identified all 48 Salmonella strains used in the inclusivity test, and did not detect all 30 non-Salmonella species tested. The method was evaluated by analyzing 120 diverse food and water samples enriched in buffered peptone water. The bipA-based real-time PCR assay showed 100% efficiency, sensitivity, and specificity compared to the invA-based method previously published, which was developed as a part of a European project for the standardization of PCR methods in food microbiology. The assay includes an independent internal amplification control (IAC) in each reaction to control false negative results. 'a9Springer Science+Business Media, LLC 2007.
机译:设计并评估了一种基于实时聚合酶链反应(PCR)的简单直接的检测方法,用于沙门氏菌的检测。在食物和水样本中。这项新的检测方法基于沙门氏菌bipA基因的特异性检测,该沙门氏菌编码三磷酸鸟苷(GTP)结合延伸家族的一种蛋白质,该蛋白质通过调节多种下游过程显示出整体的调节特性。新方法正确鉴定了包容性试验中使用的所有48株沙门氏菌,并且未检测到所有30种非沙门氏菌。通过分析120种富含蛋白p缓冲水的食品和水样来评估该方法。与之前发表的基于invA的方法相比,基于bipA的实时PCR分析显示出100%的效率,灵敏度和特异性,该方法是作为欧洲项目中食品微生物学中PCR方法标准化的一部分而开发的。该测定法在每个反应中均包括独立的内部扩增对照(IAC),以控制假阴性结果。 'a9Springer Science + Business Media,LLC 2007。

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