Dorai-Raj Siobhán, O' Grady Justin, Colleran Emer
Environmental Microbiology Research Unit, Microbiology, School of Natural Sciences, National University of Ireland, Galway, University Road, Galway, Ireland.
Water Res. 2009 Nov;43(19):4980-8. doi: 10.1016/j.watres.2009.08.050. Epub 2009 Sep 6.
Three novel ruminant-specific PCR assays, an existing ruminant-specific PCR assay and five existing human-specific PCR assays, which target 16S rDNA from Bacteroidales or Bifidobacteria, were evaluated. The assays were tested on DNA extracted from ruminant (n=74), human (n=59) and non-ruminant animal (n=44) sewage/fecal samples collected in Ireland. The three novel PCR assays compared favourably to the existing ruminant-specific assay, exhibiting sensitivities of 91-100% and specificities of 95-100% as compared to a sensitivity of 95% and specificity of 94%, for the existing ruminant-specific assay. Of the five human-specific PCR assays, the assay targeting the Bifidobacterium catenulatum group was the most promising, exhibiting a sensitivity of 100% (with human sewage samples) and a specificity of 87%. When tested on rural water samples that were naturally contaminated by ruminant feces, the three novel PCR assays tested positive with a much greater percentage (52-87%) of samples than the existing ruminant-specific assay (17%). These novel ruminant-specific assays show promise for microbial source tracking and merit further field testing and specificity evaluation.
对三种新的反刍动物特异性聚合酶链反应(PCR)检测方法、一种现有的反刍动物特异性PCR检测方法以及五种现有的人类特异性PCR检测方法进行了评估,这些方法靶向拟杆菌目或双歧杆菌的16S核糖体DNA(rDNA)。在从爱尔兰收集的反刍动物(n = 74)、人类(n = 59)和非反刍动物(n = 44)的污水/粪便样本中提取的DNA上对这些检测方法进行了测试。与现有的反刍动物特异性检测方法相比,三种新的PCR检测方法表现良好,其灵敏度为91%-100%,特异性为95%-100%,而现有的反刍动物特异性检测方法的灵敏度为95%,特异性为94%。在五种人类特异性PCR检测方法中,靶向链状双歧杆菌群的检测方法最有前景,其灵敏度为100%(对人类污水样本),特异性为87%。当在自然受到反刍动物粪便污染的农村水样上进行测试时,三种新的PCR检测方法检测呈阳性的样本百分比(52%-87%)比现有的反刍动物特异性检测方法(17%)高得多。这些新的反刍动物特异性检测方法在微生物源追踪方面显示出前景,值得进一步进行现场测试和特异性评估。