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A qPCR Assay to Detect and Quantify Shiga Toxin-Producing E. coli (STEC) in Cattle and on Farms: A Potential Predictive Tool for STEC Culture-Positive Farms

机译:在牛和农场中检测和定量产生志贺毒素的大肠杆菌(STEC)的qPCR分析:对STEC培养阳性农场的潜在预测工具

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摘要

Shiga toxin-producing E. coli (STEC), of various serogroups harboring the intimin gene, form a serious threat to human health. They are asymptomatically carried by cattle. In this study, a quantitative real-time PCR (qPCR) method was developed as a molecular method to detect and quantify Shiga toxin genes stx1 and stx2 and the intimin gene eae. Subsequently, 59 fecal samples from six farms were tested using qPCR and a culture method as a reference. Three farms had contaminated animals as demonstrated by the culture method. Culture-positive farms showed moderate significantly higher stx prevalences than culture-negative farms (p = 0.05). This is the first study which showed preliminary results that qPCR can predict STEC farm contamination, with a specificity of 77% and a sensitivity of 83%, as compared with the culture method. Furthermore, the presence or quantity of stx genes in feces was not correlated to the isolation of STEC from the individual animal. Quantitative data thus did not add value to the results. Finally, the detection of both stx and eae genes within the same fecal sample or farm using qPCR was not correlated with the isolation of an eae-harboring STEC strain from the respective sample or farm using the culture method.
机译:携带intimin基因的各种血清群产生志贺毒素的大肠杆菌(STEC)对人类健康构成了严重威胁。它们无症状地由牛携带。在这项研究中,定量实时PCR(qPCR)方法被开发为检测和定量志贺毒素基因stx1和stx2和intimin基因eae的分子方法。随后,使用qPCR和培养方法作为参考,对六个农场的59份粪便样品进行了测试。如养殖方法所示,三个农场已污染了动物。文化阳性养殖场的stx患病率显着高于文化阴性养殖场(p = 0.05)。这是第一项显示初步结果的qPCR可以预测STEC农场污染的初步结果,与培养方法相比,特异性为77%,灵敏度为83%。此外,粪便中stx基因的存在或数量与从单个动物中分离STEC无关。因此,定量数据并未为结果增加价值。最后,使用qPCR在同一粪便样品或农场中对stx和eae基因的检测与使用培养方法从相应样品或农场中分离出携带eae的STEC菌株无关。

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