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A PCR based assay for the detection of enteric pathogens from HemoccultRTM cards.

机译:一种基于PCR的检测方法,用于检测HemoccultRTM卡中的肠道病原体。

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摘要

Background. Large field studies in travelers' diarrhea (TD) in multiple destinations are limited by the need to perform stool cultures on site in a timely manner. A method for the collection, transport and storage of fecal specimens that does not require immediate processing, refrigeration and is stable for months would be advantageous.;Objectives. Determine if enteric pathogen bacterial DNA can be identified in cards routinely used for evaluation of fecal occult blood.;Methods. U.S. students traveling to Mexico in 2005-07 were followed for occurrence of diarrheal illness. When ill, students provided a stool specimen for culture and occult blood by the standard method. Cards were then stored at room temperature prior to DNA extraction. A multiplex fecal PCR was performed to identify enterotoxigenic Escherichia coli and enteroaggregative E. coli (EAEC) in DNA extracted from stools and occult blood cards.;Results. Significantly more EAEC cases were identified by PCR done in DNA extracted from cards (49%) or from frozen feces (40%) than by culture followed by HEp-2 adherence assays (13%). Similarly more ETEC cases were detected in card DNA (38%) than fecal DNA (30%) or culture followed by hybridization (10%). Sensitivity and specificity of the card test was 75% and 62%, respectively, and 50% and 63%, respectively, when compared to EAEC and ETEC culture, respectively, and 53% and 51%, respectively compared to EAEC multiplex fecal PCR and 56% and 70%, respectively, compared to ETEC multiplex fecal PCR.;Conclusions. DNA extracted from fecal cards used for detection of occult blood is of use in detecting enteric pathogens.
机译:背景。由于需要及时在现场进行粪便培养,限制了在多个目的地进行的旅行者腹泻(TD)的大型现场研究。一种不需要立即处理,冷藏并且可以稳定数月的粪便标本的收集,运输和储存方法将是有利的。确定是否可以在常规用于评估粪便潜血的卡片中鉴定出肠道病原体细菌DNA。跟踪了2005-07年前往墨西哥的美国学生出现的腹泻病。生病时,学生按标准方法提供粪便样本用于培养和隐血。然后在提取DNA之前将卡在室温下保存。进行了粪便多重PCR,以鉴定从粪便和潜血卡中提取的DNA中的产肠毒素大肠埃希氏菌和肠道聚集性大肠杆菌(EAEC)。通过PCR鉴定出的从卡片(49%)或冷冻粪便(40%)提取的DNA中进行的PCR鉴定出的EAEC病例明显多于培养,然后进行HEp-2粘附测定(13%)。同样,在卡片DNA(38%)中检测到的ETEC病例多于粪便DNA(30%)或培养后进行杂交(10%)的病例。与EAEC和ETEC培养相比,卡片测试的灵敏度和特异性分别为75%和62%,分别为50%和63%,与EAEC多重粪便PCR和PCR相比分别为53%和51%。与ETEC多重粪便PCR相比分别为56%和70%。从用于检测潜血的粪便卡中提取的DNA可用于检测肠病原体。

著录项

  • 作者

    Grimes, Kevin Anthony.;

  • 作者单位

    The University of Texas School of Public Health.;

  • 授予单位 The University of Texas School of Public Health.;
  • 学科 Biology Microbiology.;Health Sciences Public Health.
  • 学位 M.P.H.
  • 年度 2007
  • 页码 32 p.
  • 总页数 32
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:39:11

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