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首页> 外文期刊>Journal of Clinical Microbiology >PCR Detection of Escherichia coli O157:H7 Directly from Stools: Evaluation of Commercial Extraction Methods for Purifying Fecal DNA
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PCR Detection of Escherichia coli O157:H7 Directly from Stools: Evaluation of Commercial Extraction Methods for Purifying Fecal DNA

机译:直接从凳子上PCR检测大肠杆菌O157:H7:评估纯化粪便DNA的商业提取方法

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摘要

Rapid identification of Escherichia coli O157:H7 is important for patient management and for prompt epidemiological investigations. We evaluated one in-house method and three commercially available kits for their ability to extract E. coli O157:H7 DNA directly from stool specimens for PCR. Of the 153 stool specimens tested, 107 were culture positive and 46 were culture negative. The sensitivities and specificities of the in-house enrichment method, IsoQuick kit, NucliSens kit, and QIAamp kit were comparable, as follows: 83 and 98%, 85 and 100%, 74 and 98%, and 86 and 100%, respectively. False-negative PCR results may be due to the presence of either inherent inhibitors or small numbers of organisms. The presence of large amounts of bacteria relative to the amount of the E. coli O157:H7 target may result in the lower sensitivities of the assays. All commercial kits were rapid and easy to use, although DNA extracted with the QIAamp kit did not require further dilution of the DNA template prior to PCR.
机译:快速鉴定O157:H7大肠杆菌对于患者管理和及时的流行病学调查很重要。我们评估了一种内部方法和三种市售试剂盒提取 E的能力。直接从粪便标本中提取大肠杆菌O157:H7 DNA进行PCR。在测试的153个粪便样本中,有107个培养阳性,46个培养阴性。内部富集方法,IsoQuick试剂盒,NucliSens试剂盒和QIAamp试剂盒的敏感性和特异性相当,如下:分别为83%和98%,85%和100%,74%和98%,86%和100%。 PCR假阴性结果可能是由于固有抑制剂或少量生物体的存在。相对于 E的数量,存在大量细菌。大肠杆菌O157:H7靶标可能会导致检测灵敏度降低。尽管使用QIAamp试剂盒提取的DNA在PCR之前不需要进一步稀释DNA模板,但所有的商业试剂盒都是快速且易于使用的。

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