In silico analysis reveals differential targeting of enterovirus species by commonly used PCR assays

Van N Trinh, Nisha J Mulakken, Kara L Nelson, Nicholas A Be, Rose S Kantor
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Abstract

Quantitative polymerase chain reaction (qPCR) assays are sensitive molecular tools commonly used to quantify pathogens in environmental samples. These assays have become a staple of wastewater-based surveillance and often form the basis of quantitative microbial risk assessments. However, PCR assays may fail to capture all of their intended targets due to signature erosion over time. Here, we performed an in silico analysis of four human enterovirus PCR assays to assess signature erosion against the NCBI virus database. The predicted number of genomes hit by each assay rose alongside total genomes in the database through 2010 but the proportion of predicted hits began to level off with the emergence of the clinically important enterovirus D-68. We found that although all assays captured a majority of enterovirus species, only one recently developed assay adequately captured enterovirus D species. Some assays also appeared more likely to capture non-human enteroviruses than others, an important consideration for data interpretation. We conclude that broad-spectrum virus assays applied to environmental samples should be regularly checked against expanding sequence databases and provide methods to do so.
硅学分析揭示了常用 PCR 检测法对肠道病毒种类的不同靶向性
定量聚合酶链反应 (qPCR) 检测是一种灵敏的分子工具,常用于定量检测环境样本中的病原体。这些检测方法已成为废水监测的主要手段,通常也是微生物定量风险评估的基础。然而,由于随着时间的推移,PCR 检测法可能无法捕获所有预期目标。在此,我们对四种人类肠道病毒 PCR 检测方法进行了硅分析,以对照 NCBI 病毒数据库评估特征侵蚀情况。到 2010 年,每种检测方法预测命中的基因组数量都随着数据库中基因组总数的增加而增加,但随着临床上重要的肠道病毒 D-68 的出现,预测命中的比例开始趋于平稳。我们发现,尽管所有检测方法都能捕获大多数肠道病毒种类,但只有一种最近开发的检测方法能充分捕获肠道病毒 D 种类。一些检测方法似乎比其他检测方法更容易捕获非人类肠道病毒,这也是解释数据的一个重要考虑因素。我们的结论是,应用于环境样本的广谱病毒检测方法应定期与不断扩大的序列数据库进行核对,并提供核对方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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