首页> 外文期刊>Journal of Rapid Methods and Automation in Microbiology >Simultaneous direct detection of Salmonella spp., Listeria monocytogenes and Escherichia coli O157 in milk samples by magnetic extraction and multiplex PCR.
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Simultaneous direct detection of Salmonella spp., Listeria monocytogenes and Escherichia coli O157 in milk samples by magnetic extraction and multiplex PCR.

机译:磁性提取和多重PCR同时直接检测牛奶样品中的沙门氏菌,单核细胞增生李斯特菌和大肠埃希氏菌O157。

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摘要

The aim of our work was to develop a new molecular method for the simultaneous detection of Salmonella spp., Listeria monocytogenes and Escherichia coli O157 directly in milk samples. Three specific target sequences were chosen for a multiplex polymerase chain reaction (PCR) assay: a 155-bp region of the Salmonella spp. tetrathionate reductase (ttr) locus; a 173-bp region of the L. monocytogenes listeriolysin O gene (hlyA); a 217-bp region of the E. coli O157 lipopolysaccharide gene (rfbE). An internal amplification control was also included to detect PCR inhibition. In addition, a magnetic-based extraction method was also developed to isolate PCR-ready DNA from milk. The assay was able to detect, whether alone or mixed, also with a difference of 2 log units, as few as 102 cells of each pathogen per 10 mL of spiked milk.
机译:我们的工作目的是开发一种新的分子方法,用于直接在大肠杆菌中同时检测沙门氏菌,单核细胞增生李斯特菌和大肠杆菌O157。牛奶样品。选择了三个特定的靶序列进行多重聚合酶链反应(PCR)分析:沙门氏菌spp的155 bp区域。四硫酸盐还原酶( ttr )基因座; L的173bp区域。单核细胞增生李斯特菌溶血素O基因( hlyA ); E的217bp区域。大肠杆菌O157脂多糖基因(rfbE )。还包括内部扩增对照以检测PCR抑制。此外,还开发了一种基于磁性的提取方法以从牛奶中分离出可用于PCR的DNA。该测定法能够单独检测或混合检测2个log单位的差异,每10毫升加标牛奶中每种病原体只有10 2 个细胞。

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