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使用基于聚乙二醇的浓缩方法和定量逆转录聚合酶链反应对废水中的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)RNA进行浓缩和定量

Concentration and Quantification of SARS-CoV-2 RNA in Wastewater Using Polyethylene Glycol-Based Concentration and qRT-PCR.

作者信息

Farkas Kata, Hillary Luke S, Thorpe Jamie, Walker David I, Lowther James A, McDonald James E, Malham Shelagh K, Jones Davey L

机构信息

School of Natural Sciences, Bangor University, Deiniol Road, Bangor LL57 2UW, UK.

School of Ocean Sciences, Bangor University, Menai Bridge LL59 5AB, UK.

出版信息

Methods Protoc. 2021 Feb 23;4(1):17. doi: 10.3390/mps4010017.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3823/8005995/b941605ee1b9/mps-04-00017-g001.jpg

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