3.8 Article

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

期刊

METHODS AND PROTOCOLS
卷 4, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/mps4010017

关键词

COVID-19; environmental samples; sewage; wastewater virology; public health

资金

  1. UK Natural Environment Research Council (NERC) [NE/V004883/1]
  2. Soils Training and Research Studentship (STARS) grant from the Biotechnology and Biological Sciences Research Council (BBSRC)
  3. Natural Environment Research Council [NE/M009106/1]
  4. Defra Animal and Plant Health and Welfare (APHW) Official Development Assistance (ODA) COVID-19 Response Project
  5. NERC [NE/V004883/1, 1937811] Funding Source: UKRI

向作者/读者索取更多资源

Wastewater-based epidemiology is a vital tool for monitoring SARS-CoV-2 outbreaks, but the detection of viruses in sewage is challenging. A simple concentration method using PEG precipitation enables efficient detection of various viruses in wastewater, offering a comprehensive assessment of viral diseases in a community.
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 900-1500x 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.

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