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Molecular Assays for Targeting Human and Bovine Enteric Viruses in Coastal Waters and Their Application for Library-Independent Source Tracking

机译:针对沿海水域中人和牛肠道病毒的分子测定及其在独立于文库的源追踪中的应用

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摘要

Rapid population growth and urban development along waterways and coastal areas have led to decreasing water quality. To examine the effects of upstream anthropogenic activities on microbiological water quality, methods for source-specific testing are required. In this study, molecular assays targeting human enteroviruses (HEV), bovine enteroviruses (BEV), and human adenoviruses (HAdV) were developed and used to identify major sources of fecal contamination in the lower Altamaha River, Georgia. Two-liter grab samples were collected monthly from five tidally influenced stations between July and December 2002. Samples were analyzed by reverse transcription- and nested-PCR. PCR results were confirmed by dot blot hybridization. Eleven and 17 of the 30 surface water samples tested positive for HAdV and HEV, respectively. Two-thirds of the samples tested positive for either HEV or HAdV, and the viruses occurred simultaneously in 26% of samples. BEV were detected in 11 of 30 surface water samples. Binary logistic regression analysis showed that the presence of both human and bovine enteric viruses was not significantly related to either fecal coliform or total coliform levels. The presence of these viruses was directly related to dissolved oxygen and streamflow but inversely related to water temperature, rainfall in the 30 days preceding sampling, and chlorophyll-a concentrations. The stringent host specificity of enteric viruses makes them good library-independent indicators for identification of water pollution sources. Viral pathogen detection by PCR is a highly sensitive and easy-to-use tool for rapid assessment of water quality and fecal contamination when public health risk characterization is not necessary.
机译:水道和沿海地区人口的快速增长和城市发展导致水质下降。为了检查上游人为活动对微生物水质的影响,需要采用针对特定来源的测试方法。在这项研究中,针对人肠病毒(HEV),牛肠病毒(BEV)和人腺病毒(HAdV)的分子检测方法得到了开发,并用于鉴定佐治亚州Altamaha河下游粪便污染的主要来源。在2002年7月至2002年12月期间,每月从五个受潮汐影响的站点收集2升抓斗样品。通过逆转录和巢式PCR分析样品。通过斑点印迹杂交确认PCR结果。 30个地表水样品中有11个和17个分别检测出HAdV和HEV呈阳性。三分之二的样本检测出HEV或HAdV呈阳性,并且26%的样本同时发生了病毒。在30个地表水样品中的11个中检测到BEV。二元逻辑回归分析表明,人和牛肠道病毒的存在与粪便大肠菌群或总大肠菌群水平均无显着相关性。这些病毒的存在与溶解氧和水流直接相关,但与水温,采样前30天的降雨以及叶绿素a浓度成反比。肠病毒的严格宿主特异性使其成为鉴定水污染源的良好的库独立指标。通过PCR进行病毒病原体检测是一种高度敏感且易于使用的工具,可以在不需要公共卫生风险特征分析时快速评估水质和粪便污染。

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