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Quantitative PCR for Genetic Markers of Human Fecal Pollution▿

机译:人类粪便污染遗传标记的定量PCR

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摘要

Assessment of health risk and fecal bacterial loads associated with human fecal pollution requires reliable host-specific analytical methods and a rapid quantification approach. We report the development of quantitative PCR assays for quantification of two recently described human-specific genetic markers targeting Bacteroidales-like cell surface-associated genes. Each assay exhibited a range of quantification from 10 to 1 × 106 copies of target DNA. For each assay, internal amplification controls were developed to detect the presence or absence of amplification inhibitors. The assays predominantly detected human fecal specimens and exhibited specificity levels greater than 97% when tested against 265 fecal DNA extracts from 22 different animal species. The abundance of each human-specific genetic marker in primary effluent wastewater samples collected from 20 geographically distinct locations was measured and compared to quantities estimated by real-time PCR assays specific for rRNA gene sequences from total Bacteroidales and enterococcal fecal microorganisms. Assay performances combined with the prevalence of DNA targets in sewage samples provide experimental evidence supporting the potential application of these quantitative methods for monitoring fecal pollution in ambient environmental waters.
机译:评估与人类粪便污染相关的健康风险和粪便细菌负荷需要可靠的针对宿主的分析方法和快速定量方法。我们报告了定量PCR测定法的发展,用于量化两个最近描述的针对特定细菌类细菌样细胞表面相关基因的人类特异性遗传标记。每种测定均显示出10到1×106拷贝的靶DNA定量范围。对于每种测定,开发内部扩增对照以检测扩增抑制剂的存在或不存在。该测定法主要检测人类粪便样本,当针对22种不同动物的265种粪便DNA提取物进行测试时,其特异性水平高于97%。测量了从20个地理上不同的位置收集的主要废水废水样品中每个人类特异性遗传标记的丰度,并将其与通过实时PCR测定法估算的数量相比较,该实时PCR测定法对总细菌和肠球菌粪便微生物的rRNA基因序列具有特异性。分析性能与污水样品中DNA靶标的普遍性相结合,提供了实验证据,支持了这些定量方法在监测周围环境水域粪便污染方面的潜在应用。

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