Kristina M Babler, Mark E Sharkey, Ayaaz Amirali, Melinda M Boone, Samuel Comerford, Benjamin B Currall, George S Grills, Jennifer Laine, Christopher E Mason, Brian Reding, Stephan Schürer, Mario Stevenson, Dušica Vidović, Sion L Williams, Helena M Solo-Gabriele
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The objective of this study was to establish the necessary steps for isolating DNA from wastewater by modifying a long-standing RNA-specific extraction workflow optimized for SARS-CoV-2 detection. Modifications were made to the sample concentration process and included an evaluation of bead bashing prior to the extraction of either DNA or RNA. Results showed that bead bashing reduced detection of RNA from wastewater but improved recovery of DNA as assessed by quantitative polymerase chain reaction (qPCR). Bead bashing is therefore not recommended for the quantification of RNA viruses using qPCR. Whereas for Mycobacterium bacterial DNA isolation, bead bashing was necessary for improving qPCR quantification. Overall, we recommend 2 separate workflows, one for RNA viruses that does not include bead bashing and one for other microbes that use bead bashing for DNA isolation. 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引用次数: 0
摘要
废水监测(WBS)是一种非侵入性的流行病学策略,用于评估 COVID-19 在社区中的传播情况。该策略基于对病毒目标--严重急性呼吸系统综合症冠状病毒 2(SARS-CoV-2)的废水 RNA 测量。WBS 在评估 COVID-19 传播方面的实用性促使研究人员测量 SARS-CoV-2 以外的目标,包括含有 DNA 的病原体。本研究的目的是通过修改长期以来针对 SARS-CoV-2 检测而优化的 RNA 特异性提取工作流程,确定从废水中分离 DNA 的必要步骤。对样品浓缩过程进行了修改,包括在提取 DNA 或 RNA 之前对压珠进行评估。结果表明,压珠减少了废水中 RNA 的检测,但通过定量聚合酶链反应 (qPCR) 评估,提高了 DNA 的回收率。因此,不建议使用 qPCR 对 RNA 病毒进行定量。而对于分枝杆菌细菌 DNA 的分离,为了提高 qPCR 的定量效果,必须对珠子进行敲打。总之,我们建议采用两种不同的工作流程,一种用于不包括撞珠的 RNA 病毒,另一种用于使用撞珠进行 DNA 分离的其他微生物。这里所做的实验表明,目前针对 SARS-CoV-2 优化的 WBS 程序方法需要修改和重新优化,以便随时检测和监测其他病原体,从而扩大其作为公共卫生评估工具的效用。
Expanding a Wastewater-Based Surveillance Methodology for DNA Isolation from a Workflow Optimized for SARS-CoV-2 RNA Quantification.
Wastewater-based surveillance (WBS) is a noninvasive, epidemiological strategy for assessing the spread of COVID-19 in communities. This strategy was based upon wastewater RNA measurements of the viral target, severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). The utility of WBS for assessing the spread of COVID-19 has motivated research to measure targets beyond SARS-CoV-2, including pathogens containing DNA. The objective of this study was to establish the necessary steps for isolating DNA from wastewater by modifying a long-standing RNA-specific extraction workflow optimized for SARS-CoV-2 detection. Modifications were made to the sample concentration process and included an evaluation of bead bashing prior to the extraction of either DNA or RNA. Results showed that bead bashing reduced detection of RNA from wastewater but improved recovery of DNA as assessed by quantitative polymerase chain reaction (qPCR). Bead bashing is therefore not recommended for the quantification of RNA viruses using qPCR. Whereas for Mycobacterium bacterial DNA isolation, bead bashing was necessary for improving qPCR quantification. Overall, we recommend 2 separate workflows, one for RNA viruses that does not include bead bashing and one for other microbes that use bead bashing for DNA isolation. The experimentation done here shows that current-standing WBS program methodologies optimized for SARS-CoV-2 need to be modified and reoptimized to allow for alternative pathogens to be readily detected and monitored, expanding its utility as a tool for public health assessment.