Evidence map›Paper›PMID 34252764›Full record

ArticleThe Science of the total environment2021

A direct capture method for purification and detection of viral nucleic acid enables epidemiological surveillance of SARS-CoV-2.

Subhanjan Mondal, Nathan Feirer, Michael Brockman, Melanie A Preston, Sarah J Teter, Dongping Ma, Said A Goueli, Sameer Moorji, Brigitta Saul, James J Cali

Open access · hybridAbstract read
In one paragraph

Article in The Science of the total environment, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 3 pooled it
3.7field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 3 syntheses or guidelines pooled it, 68 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Subhanjan MondalPromega Corporation, 5430 E Cheryl Pkwy, Fitchburg, WI 53711, United States of America. Electronic address: subhanjan.mondal@promega.com.
Nathan FeirerPromega Corporation, 5430 E Cheryl Pkwy, Fitchburg, WI 53711, United States of America.
Michael BrockmanPromega Corporation, 5430 E Cheryl Pkwy, Fitchburg, WI 53711, United States of America.
Melanie A PrestonPromega Corporation, 5430 E Cheryl Pkwy, Fitchburg, WI 53711, United States of America.
Sarah J TeterPromega Corporation, 5430 E Cheryl Pkwy, Fitchburg, WI 53711, United States of America.
Dongping MaPromega Corporation, 5430 E Cheryl Pkwy, Fitchburg, WI 53711, United States of America.
Said A GoueliPromega Corporation, 5430 E Cheryl Pkwy, Fitchburg, WI 53711, United States of America.
Sameer MoorjiPromega Corporation, 5430 E Cheryl Pkwy, Fitchburg, WI 53711, United States of America.
Brigitta SaulPromega Corporation, 5430 E Cheryl Pkwy, Fitchburg, WI 53711, United States of America.
James J CaliPromega Corporation, 5430 E Cheryl Pkwy, Fitchburg, WI 53711, United States of America.
Promega (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studies have demonstrated that SARS-CoV-2 RNA can be detected in the feces of infected individuals. This finding spurred investigation into using wastewater-based epidemiology (WBE) to monitor SARS-CoV-2 RNA and track the appearance and spread of COVID-19 in communities. SARS-CoV-2 is present at low levels in wastewater, making sample concentration a prerequisite for sensitive detection and utility in WBE. Whereas common methods for isolating viral genetic material are biased toward intact virus isolation, it is likely that a relatively low percentage of the total SARS-CoV-2 RNA genome in wastewater is contained within intact virions. Therefore, we hypothesized that a direct unbiased total nucleic acid(TNA) extraction method could overcome the cumbersome protocols, variability and low recovery rates associated with the former methods. This led to development of a simple, rapid, and modular alternative to existing purification methods. In an initial concentration step, chaotropic agents are added to raw sewage allowing binding of nucleic acid from free nucleoprotein complexes, partially intact, and intact virions to a silica matrix. The eluted nucleic acid is then purified using manual or semi-automated methods. RT-qPCR enzyme mixes were formulated that demonstrate substantial inhibitor resistance. In addition, multiplexed probe-based RT-qPCR assays detecting the N1, N2 (nucleocapsid) and E (envelope) gene fragments of SARS-CoV-2 were developed. The RT-qPCR assays also contain primers and probes to detect Pepper Mild Mottle Virus (PMMoV), a fecal indicator RNA virus present in wastewater, and an exogenous control RNA to measure effects of RT-qPCR inhibitors. Using this workflow, we monitored wastewater samples from three wastewater treatment plants (WWTP) in Dane County, Wisconsin. We also successfully sequenced a subset of samples to ensure compatibility with a SARS-CoV-2 amplicon panel and demonstrated the potential for SARS-CoV-2 variant detection. Data obtained here underscore the potential for wastewater surveillance of SARS-CoV-2 and other infectious agents in communities.

Indexed as

COVID-19Nucleic AcidsHumansRNA, ViralSARS-CoV-2Nucleic AcidsRNA, ViralCOVID-19Nucleic acid purificationRT-qPCRSARS-CoV-2WastewaterWastewater-based epidemiology

Identifiers

PMID34252764
PMCPMC8262391
OpenAlexW3182961693

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.