Farkas Kata, Hillary Luke S, Thorpe Jamie, Walker David I, Lowther James A, McDonald James E, Malham Shelagh K, Jones Davey L
School of Natural Sciences, Bangor University, Deiniol Road, Bangor LL57 2UW, UK.
School of Ocean Sciences, Bangor University, Menai Bridge LL59 5AB, UK.
Methods Protoc. 2021 Feb 23;4(1):17. doi: 10.3390/mps4010017.
Wastewater-based epidemiology has become an important tool for the surveillance of SARS-CoV-2 outbreaks. However, the detection of viruses in sewage is challenging and to date there is no standard method available which has been validated for the sensitive detection of SARS-CoV-2. In this paper, we describe a simple concentration method based on polyethylene glycol (PEG) precipitation, followed by RNA extraction and a one-step quantitative reverse transcription PCR (qRT-PCR) for viral detection in wastewater. PEG-based concentration of viruses is a simple procedure which is not limited by the availability of expensive equipment and has reduced risk of disruption to consumable supply chains. The concentration and RNA extraction steps enable 900-1500× concentration of wastewater samples and sufficiently eliminates the majority of organic matter, which could inhibit the subsequent qRT-PCR assay. Due to the high variation in the physico-chemical properties of wastewater samples, we recommend the use of process control viruses to determine the efficiency of each step. This procedure enables the concentration and the extraction the DNA/RNA of different viruses and hence can be used for the surveillance of different viral targets for the comprehensive assessment of viral diseases in a community.
基于废水的流行病学已成为监测严重急性呼吸综合征冠状病毒2(SARS-CoV-2)疫情的重要工具。然而,在污水中检测病毒具有挑战性,迄今为止,尚无经过验证的用于灵敏检测SARS-CoV-2的标准方法。在本文中,我们描述了一种基于聚乙二醇(PEG)沉淀的简单浓缩方法,随后进行RNA提取,并采用一步法定量逆转录聚合酶链反应(qRT-PCR)来检测废水中的病毒。基于PEG的病毒浓缩是一个简单的过程,不受昂贵设备可用性的限制,并且降低了消耗品供应链中断的风险。浓缩和RNA提取步骤可使废水样本浓缩900 - 1500倍,并充分去除大部分可能抑制后续qRT-PCR检测的有机物。由于废水样本的物理化学性质差异很大,我们建议使用过程控制病毒来确定每个步骤的效率。该方法能够浓缩和提取不同病毒的DNA/RNA,因此可用于监测不同的病毒靶点,以全面评估社区中的病毒性疾病。