首页> 美国卫生研究院文献>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
【2h】

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富集培养后,使用PCR试纸DNA色谱法检测多种食源性病原体的新协议

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

A quick foodborne pathogen screening method after six-hour enrichment culture with a broad-range food pathogen enrichment broth is described. Pathogenic factors of Salmonella enterica, Shigella spp., enteroinvasive Escherichia coli, and enterohemorrhagic E. coli are 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 for S. enterica and 3.3 CFU/25 g for enterohemorrhagic E. coli in 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。用鸡尾酒引物和快速聚合酶链反应(PCR)扩增肠炎沙门氏菌,志贺氏菌属,肠侵袭性大肠杆菌和肠出血性大肠杆菌的致病因子,并在30分钟内完成扩增。 PCR扩增子在5-10分钟内用量油尺DNA色谱法进行了区分。从4到6个小时的富集培养开始,该测定在45分钟内完成。在加标的碎肉实验中,该方案对肠炎链球菌的检测灵敏度小于2.5 CFU /25μg,对肠出血性大肠杆菌的检测灵敏度小于3.3 CFU /25μg。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号