首页> 美国卫生研究院文献>Food Science of Animal Resources >Simultaneous Detection of Listeria monocytogenes Escherichia coli O157:H7 Bacillus cereus Salmonella spp. and Staphylococcus aureus in Low-fatted Milk by Multiplex PCR
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Simultaneous Detection of Listeria monocytogenes Escherichia coli O157:H7 Bacillus cereus Salmonella spp. and Staphylococcus aureus in Low-fatted Milk by Multiplex PCR

机译:多重PCR同时检测低脂牛奶中的李斯特菌单核细胞增生李斯特菌大肠杆菌O157:H7蜡状芽孢杆菌沙门氏菌和金黄色葡萄球菌

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摘要

A rapid and specific PCR assay for the simultaneous detection of Listeria monocytogenes, Escherichia coli O157:H7, Bacillus cereus, Salmonella spp., and Staphylococcus aureus in foods was developed to reduce the detection time and to increase sensitivity. Multiplex PCR developed in this study produced only actA, fliC, hbl, invA, ileS amplicons, but did not produce any non-specific amplicon. The primer sets successfully amplified the target genes in the multiplex PCR without any non-specific or additional bands on the other strains. The multiplex PCR assays also amplified some target genes from five pathogens, and multiplex amplification was obtained from as little as 1 pg of DNA. According to the results from the sensitivity evaluation, the multiplex PCR developed in this study detected 10 cells/mL of the pathogens inoculated in milk samples, respectively. The results suggested that multiplex PCR was an effective assay demonstrating high specificity for the simultaneous detection of five target pathogens in food system.
机译:为了减少检测时间并提高灵敏度,开发了一种快速且特异性的PCR检测方法,用于同时检测食品中的单核细胞增生李斯特菌,大肠杆菌O157:H7,蜡状芽孢杆菌,沙门氏菌和金黄色葡萄球菌。在这项研究中开发的多重PCR仅产生actA,fliC,hbl,invA,ileS扩增子,但不产生任何非特异性扩增子。引物组在多重PCR中成功扩增了目标基因,而在其他菌株上没有任何非特异性或附加条带。多重PCR分析还从五种病原体中扩增了一些靶基因,并且从低至1 pg的DNA获得了多重扩增。根据敏感性评估的结果,本研究开发的多重PCR分别检测了牛奶样品中接种的10个细胞/ mL的病原体。结果表明,多重PCR是一种有效的检测方法,显示了同时检测食品系统中五种目标病原体的高特异性。

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