Protocol to longitudinally quantify SARS-CoV-2 RNA in wastewater using RT-qPCR and pepper mild mottle virus normalization

被引:0
|
作者
Jimenez, Bryan Sanchez [1 ,3 ]
Sterling, Trinity [1 ]
Brown, Austin [1 ]
Modica, Brian [1 ]
Gibson, Kaylee [1 ]
Collins, Hannah [1 ]
Koch, Carolyn [1 ]
Schwarz, Tyler [1 ]
Dye, Kristine N. [1 ,2 ]
机构
[1] Stetson Univ, Dept Hlth Sci, 421 N Woodland Blvd, Deland, FL 32723 USA
[2] Stetson Univ, Dept Biol, 421 N Woodland Blvd, Deland, FL 32723 USA
[3] New York Med Coll, Dept Microbiol & Immunol, 40 Sunshine Cottage Rd, Valhalla, NY 10595 USA
来源
STAR PROTOCOLS | 2024年 / 5卷 / 02期
关键词
Environmental sciences; Microbiology; Molecular Biology;
D O I
10.1016/j.xpro.2024.103001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Wastewater surveillance allows severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection levels to be tracked in a community. Here, we present a protocol to longitudinally quantify SARS-CoV-2 RNA in wastewater using quantitative reverse -transcription PCR (RT-qPCR) and pepper mild mottle virus (PMMoV) normalization. We describe steps for the pasteurization of wastewater samples, solids separation, supernatant filtration, viral precipitation and concentration, and RNA extraction. We then detail procedures for RT-qPCR, viral concentration extrapolation, PMMoV normalization, and longitudinal analysis. This protocol has the potential to be used for surveillance of other microorganisms. For complete details on the use and execution of this protocol, please refer to Sanchez Jimenez et al. 1
引用
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页数:24
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