Direct wastewater extraction as a simple and effective method for SARS-CoV-2 surveillance and COVID-19 community-level monitoring.

FEMS microbes Pub Date : 2023-01-12 eCollection Date: 2023-01-01 DOI:10.1093/femsmc/xtad004
Megan E J Lott, William A Norfolk, Cody A Dailey, Amelia M Foley, Carolina Melendez-Declet, Megan J Robertson, Stephen L Rathbun, Erin K Lipp
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Abstract

Wastewater surveillance has proven to be an effective tool to monitor the transmission and emergence of infectious agents at a community scale. Workflows for wastewater surveillance generally rely on concentration steps to increase the probability of detection of low-abundance targets, but preconcentration can substantially increase the time and cost of analyses while also introducing additional loss of target during processing. To address some of these issues, we conducted a longitudinal study implementing a simplified workflow for SARS-CoV-2 detection from wastewater, using a direct column-based extraction approach. Composite influent wastewater samples were collected weekly for 1 year between June 2020 and June 2021 in Athens-Clarke County, Georgia, USA. Bypassing any concentration step, low volumes (280 µl) of influent wastewater were extracted using a commercial kit, and immediately analyzed by RT-qPCR for the SARS-CoV-2 N1 and N2 gene targets. SARS-CoV-2 viral RNA was detected in 76% (193/254) of influent samples, and the recovery of the surrogate bovine coronavirus was 42% (IQR: 28%, 59%). N1 and N2 assay positivity, viral concentration, and flow-adjusted daily viral load correlated significantly with per-capita case reports of COVID-19 at the county-level (ρ = 0.69-0.82). To compensate for the method's high limit of detection (approximately 106-107 copies l-1 in wastewater), we extracted multiple small-volume replicates of each wastewater sample. With this approach, we detected as few as five cases of COVID-19 per 100 000 individuals. These results indicate that a direct-extraction-based workflow for SARS-CoV-2 wastewater surveillance can provide informative and actionable results.

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直接废水提取是SARS-CoV-2监测和新冠肺炎社区级监测的一种简单有效的方法。
废水监测已被证明是在社区范围内监测传染源传播和出现的有效工具。废水监测的工作流程通常依赖于浓缩步骤来增加检测低丰度目标的概率,但预浓缩可以显著增加分析的时间和成本,同时在处理过程中还会引入额外的目标损失。为了解决其中的一些问题,我们进行了一项纵向研究,使用基于直接柱的提取方法,实现了从废水中检测严重急性呼吸系统综合征冠状病毒2型的简化工作流程。2020年6月至2021年6月,在美国佐治亚州雅典克拉克县每周采集一次复合进水废水样本,为期一年。通过任何浓缩步骤,使用商业试剂盒提取低体积(280µl)的进水废水,并立即通过RT-qPCR分析严重急性呼吸系统综合征冠状病毒2型N1和N2基因靶标。在76%(193/254)的进水样本中检测到严重急性呼吸系统综合征冠状病毒2型病毒RNA,替代牛冠状病毒的回收率为42%(IQR:28%,59%)。N1和N2检测阳性率、病毒浓度和流量调整后的每日病毒载量与县级新冠肺炎的每个病例报告显著相关(ρ=0.69-0.82)。为了补偿该方法的高检测限(废水中约106-107个拷贝l-1),我们提取了每个废水样本的多个小容量复制品。通过这种方法,我们每10万人中只检测到5例新冠肺炎病例。这些结果表明,基于直接提取的严重急性呼吸系统综合征冠状病毒2型废水监测工作流程可以提供信息和可操作的结果。
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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来源期刊
CiteScore
3.30
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审稿时长
15 weeks
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