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加利福尼亚雨水流域中人类病毒的分子定量分析。

Molecular quantitative analysis of human viruses in California stormwater.

作者信息

Rajal V B, McSwain B S, Thompson D E, Leutenegger C M, Wuertz S

机构信息

Department of Civil and Environmental Engineering, University of California, Davis, One Shields Avenue, Davis, CA 95616, USA.

出版信息

Water Res. 2007 Nov;41(19):4287-98. doi: 10.1016/j.watres.2007.06.002. Epub 2007 Jun 20.

Abstract

Many human pathogenic viruses are transmitted via the oral-fecal route and water is one possible vector, representing a risk for public health. Sixty-one large-volume water samples from storm drains in California were processed by a two-step hollow fiber ultrafiltration procedure followed by molecular analysis for human enterovirus and adenovirus types. Each sample was spiked with a surrogate, the benign bacteriophage PP7. Both surrogate and human viruses were quantified by newly designed TaqMan PCR assays. Equations were developed that account for the main variables in the procedure: recovery of the ultrafiltration, efficiency of nucleic acid extraction, and effect of inhibitors on the amplification of viral targets. Adenovirus 40/41 was detected in one sample at 230 genomes per liter, and no other adenovirus or enterovirus types were found. Samples that resulted in nondetects are reported together with the corresponding sample-specific limit of detection (S(LOD)), a useful tool when estimating the public health risk associated with the contact or ingestion of water. Virus concentrations did not correlate with traditional viable indicator concentrations or any of the physicochemical parameters measured. In contrast, coliform concentrations were correlated with total suspended solids. To our knowledge, this is the first study where all factors known to influence limits of detection have been investigated and integrated into equations that are widely applicable to the quantification of viruses or other microbial targets by PCR.

摘要

许多人类致病病毒通过粪口途径传播,水是一种可能的传播媒介,对公众健康构成风险。对加利福尼亚州雨水排放口采集的61份大体积水样进行两步中空纤维超滤处理,随后对人肠道病毒和腺病毒类型进行分子分析。每个样品都加入了替代物——良性噬菌体PP7。通过新设计的TaqMan PCR检测法对替代物和人类病毒进行定量。建立了考虑该过程中主要变量的方程:超滤回收率、核酸提取效率以及抑制剂对病毒靶标扩增的影响。在一个样品中检测到腺病毒40/41,浓度为每升230个基因组,未发现其他腺病毒或肠道病毒类型。报告了未检测到病毒的样品及其相应的样品特异性检测限(S(LOD)),这是评估与接触或摄入水相关的公共卫生风险时的一个有用工具。病毒浓度与传统的活菌指示物浓度或所测的任何理化参数均无相关性。相比之下,大肠菌群浓度与总悬浮固体相关。据我们所知,这是第一项对所有已知影响检测限的因素进行研究并将其整合到广泛适用于通过PCR对病毒或其他微生物靶标进行定量的方程中的研究。

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