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首页> 外文期刊>Journal of Food Safety >Comparison of a real-time polymerase chain reaction assay with a culture method for the detection of Salmonella in retail meat samples.
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Comparison of a real-time polymerase chain reaction assay with a culture method for the detection of Salmonella in retail meat samples.

机译:实时聚合酶链反应分析与培养方法在零售肉类样品中沙门氏菌检测的比较。

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摘要

A novel real-time PCR method is described and compared with a conventional International Organization for Standardization culture method for the detection of Salmonella in Irish beef, chicken meat, pork and turkey meat. After selective enrichment, all meat samples (n = 100) were subjected to DNA extraction and real-time PCR analysis using primers against a Salmonella spp. specific gene (16S rRNA) or the invA virulence gene, and plated on differential media and identified as Salmonella using immunological and subtyping methods. Retail samples (5/100) were found to contain Salmonella using the 16S rRNA gene-based real-time PCR assay and the standard culture method. However, only 2 of 5 samples were found to contain Salmonella using the invA gene-based real-time PCR assay. For the sample set examined, the developed 16S rRNA gene-based real-time PCR assay demonstrated comparable specificity and sensitivity to the currently used standard culture method but was considerably more rapid.
机译:描述了一种新颖的实时PCR方法,并将其与用于检测爱尔兰牛肉,鸡肉,猪肉和火鸡肉中沙门氏菌的常规国际标准化组织培养方法进行了比较。选择性富集后,使用针对沙门氏菌的引物对所有肉类样品(n = 100)进行DNA提取和实时PCR分析。特异性基因(16S rRNA)或invA毒力基因,并接种在差异培养基上,并使用免疫学和亚型方法鉴定为沙门氏菌。使用基于16S rRNA基因的实时PCR分析和标准培养方法,发现零售样品(5/100)中含有沙门氏菌。但是,使用基于invA基因的实时PCR测定法,发现5个样本中只有2个含有沙门氏菌。对于所检查的样品集,已开发的基于16S rRNA基因的实时PCR分析方法显示了与当前使用的标准培养方法相当的特异性和敏感性,但速度更快。

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