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首页> 外文期刊>BioMed research international >A New Protocol to Detect Multiple Foodborne Pathogens with PCR Dipstick DNA Chromatography after a Six-Hour Enrichment Culture in a Broad-Range Food Pathogen Enrichment Broth
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A New Protocol to Detect Multiple Foodborne Pathogens with PCR Dipstick DNA Chromatography after a Six-Hour Enrichment Culture in a Broad-Range Food Pathogen Enrichment Broth

机译:在广泛的食物病原体富集肉汤中进行六小时浓缩培养后,用PCR试纸DNA色谱法检测多种食源性病原体的新协议

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A quick foodborne pathogen screening method after six-hour enrichment culture with a broad-range food pathogen enrichment broth is described. Pathogenic factors ofSalmonella enterica,Shigellaspp., enteroinvasiveEscherichia coli, and enterohemorrhagicE. coliare amplified with a cocktail primer and rapid polymerase chain reaction (PCR), which finishes amplification in 30 min. The PCR amplicon was differentiated with a dipstick DNA chromatography assay in 5–10 min. Starting from a four- to six-hour enrichment culture, this assay was finished within 45 min. Detection sensitivity of this protocol was less than 2.5 CFU/25 g forS. entericaand 3.3 CFU/25 g for enterohemorrhagicE. coliin spiked ground meat experiments.
机译:描述了用广泛的食物病原体富集肉汤进行六小时富集培养后的快速食源性病原体筛选方法。肠沙门氏菌,志贺氏菌,肠侵袭性大肠杆菌和肠出血性大肠杆菌的致病因素。用鸡尾酒引物和快速聚合酶链反应(PCR)扩增大肠埃希菌,在30分钟内完成扩增。 PCR扩增子在5-10分钟内用量尺DNA色谱分析进行了区分。从4到6个小时的富集培养开始,此分析在45分钟内完成。该方案对S的检测灵敏度小于2.5 CFU / 25 g。肠出血和3.3 CFU / 25 g用于肠出血。大肠菌素加标的碎肉实验。

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