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Assessing the Occurrence of Waterborne Viruses in Reuse Systems: Analytical Limits and Needs

机译:评估重复使用系统中水传播病毒的发生:分析极限和需求

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摘要

Detection of waterborne enteric viruses is an essential tool in assessing the risk of waterborne transmission. Cell culture is considered a gold standard for detection of these viruses. However, it is important to recognize the uncertainty and limitations of enteric virus detection in cell culture. Cell culture cannot support replication of all virus types and strains, and numerous factors control the efficacy of specific virus detection assays, including chemical additives, cell culture passage number, and sequential passage of a sample in cell culture. These factors can result in a 2- to 100-fold underestimation of virus infectivity. Molecular methods reduce the time for detection of viruses and are useful for detection of those that do not produce cytopathogenic effects. The usefulness of polymerase chain reaction (PCR) to access virus infectivity has been demonstrated for only a limited number of enteric viruses and is limited by an understanding of the mechanism of virus inactivation. All of these issues are important to consider when assessing waterborne infectious viruses and expected goals on virus reductions needed for recycled water. The use of safety factors to account for this may be useful to ensure that the risks in drinking water and recycled water for potable reuse are minimized.
机译:水性肠道病毒的检测是评估水性传播风险的重要工具。细胞培养被认为是检测这些病毒的金标准。但是,重要的是要认识到细胞培养中肠道病毒检测的不确定性和局限性。细胞培养不能支持所有病毒类型和株的复制,并且许多因素控制特定病毒检测测定的功效,包括化学添加剂,细胞培养传代次数和样品在细胞培养中的连续传代。这些因素可能导致病毒感染率低估2至100倍。分子方法减少了检测病毒的时间,可用于检测不产生细胞致病作用的病毒。聚合酶链反应(PCR)用于访问病毒感染性的有效性仅在有限数量的肠病毒中得到证实,并且受病毒灭活机理的限制。所有这些问题在评估水性传染性病毒以及减少循环水所需的减少病毒的预期目标时都必须考虑。使用安全系数来解决此问题可能对确保将饮用水和循环水用于饮用水再利用的风险降到最低有帮助。

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