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Multiplex Quantitative PCR Assays for the Detection and Quantification of the Six Major Non-0157 Escherichia coli Serogroups in Cattle Feces

机译:牛粪便中六种主要的非0157大肠杆菌血清群的检测和定量的多重定量PCR分析

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摘要

Shiga toxin-producing Escherichia coli (STEC) serogroups O26, O45, O103, O111, O121, and O145, called non-O157 STEC, are important foodborne pathogens. Cattle, a major reservoir, harbor the organisms in the hindgut and shed them in the feces. Although limited data exist on fecal shedding, concentrations of non-O157 STEC in feces have not been reported. The objectives of our study were (ⅰ) to develop and validate two multiplex quantitative PCR (mqPCR) assays, targeting O-antigen genes of O26, O103, and O111 (mqPCR-1) and O45, O121, and O145 (mqPCR-2); (ⅱ) to utilize the two assays, together with a previously developed four-plex qPCR assay (mqPCR-3) targeting the O157 antigen and three virulence genes (stx_1, stx_2, and eae), to quantify seven serogroups and three virulence genes in cattle feces; and (ⅲ) to compare the three mqPCR assays to a 10-plex conventional PCR (cPCR) targeting seven serogroups and three virulence genes and culture methods to detect seven E. coli serogroups in cattle feces. The two mqPCR assays (1 and 2) were shown to be specific to the target genes, and the detection limits were 4 and 2 log CFU/g of pure culture-spiked fecal samples, before and after enrichment, respectively. A total of 576 fecal samples collected from a feedlot were enriched in E. coli broth and were subjected to quantification (before enrichment) and detection (after enrichment). Of the 576 fecal samples subjected, before enrichment, to three mqPCR assays for quantification, 175 (30.4%) were quantifiable (≥4 log CFU/g) for at least one of the seven serogroups, with O157 being the most common serogroup. The three mqPCR assays detected higher proportions of postenriched fecal samples (P < 0.01) as positive for one or more serogroups compared with cPCR and culture methods. This is the first study to assess the applicability of qPCR assays to detect and quantify six non-0157 serogroups in cattle feces and to generate data on fecal concentration of the six serogroups.
机译:产生志贺毒素的大肠杆菌(STEC)血清群O26,O45,O103,O111,O121和O145被称为非O157 STEC,是重要的食源性病原体。牛是主要的水库,在后肠中藏有生物,并在粪便中将它们排出。尽管关于粪便脱落的数据有限,但尚未报告粪便中非O157 STEC的浓度。我们研究的目的是(ⅰ)开发和验证两种针对O26,O103和O111(mqPCR-1)和O45,O121和O145(mqPCR-2)的O抗原基因的多重定量PCR(mqPCR)分析); (ⅱ)利用这两种测定方法,以及先前开发的针对O157抗原和三个毒力基因(stx_1,stx_2和eae)的四重qPCR测定法(mqPCR-3),来定量检测7个血清群和三个毒力基因。牛粪(ⅲ)将三种mqPCR分析方法与针对七个血清群和三个毒力基因的10重常规PCR(cPCR)进行比较,并采用培养方法检测牛粪中的七个大肠杆菌血清群。两种mqPCR分析(1和2)显示对靶基因具有特异性,在富集之前和之后,检测限分别是纯培养物粪便样品的4和2 log CFU / g。从饲养场收集的总共576个粪便样品在大肠杆菌肉汤中富集,并进行定量(富集前)和检测(富集后)。在576个粪便样品中,富集前进行了3个mqPCR测定以进行定量,其中七个血清组中的至少一个可以定量(至少4 log CFU / g)175个(30.4%),其中O157是最常见的血清组。与cPCR和培养方法相比,三种mqPCR分析检测到的一种或多种血清群的粪便样品富集率更高(P <0.01)。这是第一项评估qPCR测定法在检测和定量牛粪中6个非0157血清群并生成6个血清群粪便浓度数据方面的适用性的研究。

著录项

  • 来源
    《Journal of food protection》 |2016年第1期|66-74|共9页
  • 作者单位

    Department of Diagnostic Medicine and Pathobiology Kansas State University, Manhattan, Kansas 66506, USA;

    Department of Diagnostic Medicine and Pathobiology Kansas State University, Manhattan, Kansas 66506, USA;

    Department of Diagnostic Medicine and Pathobiology Kansas State University, Manhattan, Kansas 66506, USA;

    Veterinary Diagnostic Laboratory, Kansas State University, Manhattan, Kansas 66506, USA;

    Department of Diagnostic Medicine and Pathobiology Kansas State University, Manhattan, Kansas 66506, USA;

    Department of Diagnostic Medicine and Pathobiology Kansas State University, Manhattan, Kansas 66506, USA;

    Department of Diagnostic Medicine and Pathobiology Kansas State University, Manhattan, Kansas 66506, USA;

    Veterinary Diagnostic Laboratory, Kansas State University, Manhattan, Kansas 66506, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 23:24:43

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