Evidence map›Paper›PMID 42655739›Full record

ArticleViruses2026

Wastewater-Based Genomic Surveillance of SARS-CoV-2 Antiviral Resistance Determinants in Ontario: Towards a Scalable Framework for Population-Level Antiviral Resistance Monitoring.

Opeyemi U Lawal, Valeria R Parreira, Alyssa K Overton, Jennifer J Knapp, Richard Gibson, Eric J Arts, Linkang Zhang, Fozia Rizvi, Melinda Precious, Trevor C Charles and 1 more

Abstract read
In one paragraph

Article in Viruses, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Opeyemi U LawalGreat Lakes Institute for Environmental Research, University of Windsor, Windsor, ON N9P 3P4, Canada.ORCID 0000-0003-2352-2832
Valeria R ParreiraCanadian Research Institute for Food Safety, Department of Food Science, University of Guelph, Guelph, ON N1G 2W1, Canada.
Alyssa K OvertonDepartment of Biology, University of Waterloo, Waterloo, ON N2L 3G1, Canada.ORCID 0000-0001-7134-3551
Jennifer J KnappDepartment of Biology, University of Waterloo, Waterloo, ON N2L 3G1, Canada.ORCID 0000-0003-3347-4686
Richard GibsonDepartment of Microbiology and Immunology, Western University, London, ON N6A 3K7, Canada.ORCID 0000-0002-9569-2366
Eric J ArtsDepartment of Microbiology and Immunology, Western University, London, ON N6A 3K7, Canada.
Linkang ZhangCanadian Research Institute for Food Safety, Department of Food Science, University of Guelph, Guelph, ON N1G 2W1, Canada.
Fozia RizviCanadian Research Institute for Food Safety, Department of Food Science, University of Guelph, Guelph, ON N1G 2W1, Canada.ORCID 0000-0002-3049-7009
Melinda PreciousCanadian Research Institute for Food Safety, Department of Food Science, University of Guelph, Guelph, ON N1G 2W1, Canada.ORCID 0009-0002-4491-9097
Trevor C CharlesDepartment of Biology, University of Waterloo, Waterloo, ON N2L 3G1, Canada.
Lawrence GoodridgeCanadian Research Institute for Food Safety, Department of Food Science, University of Guelph, Guelph, ON N1G 2W1, Canada.ORCID 0009-0008-9965-3509

Funding

Integrated Network for the Surveillance of Pathogens: Increasing REsilience and capacity in Canada's pandemic response grant no. CBRF2-70 2023-00008
6 · The paper itself

Abstract

backgroundWastewater surveillance has emerged as an effective tool for population-level pathogen monitoring. Its application to mutations associated with resistance to antivirals remains comparatively underdeveloped. We assessed the wastewater epidemiology framework using SARS-CoV-2 as a model pathogen to evaluate spatial, temporal, and therapeutic class-specific resistance dynamics.

methodsWe analyzed about 10,000 SARS-CoV-2-positive wastewater samples from six Ontario public health regions collected between October 2021 and July 2024. Fifty-five mutations were screened, comprising therapeutic resistance-associated mutations and a biologically distinct group of immune-evasion mutations. Mutations detected in ≥10 samples at ≥1% frequency were retained for spatiotemporal analysis using LOESS smoothing and Kruskal-Wallis testing.

resultsTwelve mutations met the inclusion thresholds. S:E340D, associated with reduced susceptibility to sotrovimab was geographically widespread but transient and low-frequency. Five remdesivir-associated polymerase mutations were sporadic with sharp localized peaks, including two mutations exceeding 99% frequency in isolated catchments. Three nirmatrelvir-associated protease mutations were detected, with ORF1a:Q3452K showing significant regional variation. FLiRT and FLuQE immune-evasion mutations were most persistent and abundant. LOESS smoothing showed distinct temporal patterns among mutations, while Kruskal-Wallis testing identified significant regional variation for ORF1a:Q3452K and the three immune-evasion mutations.

conclusionsThese findings demonstrate that wastewater surveillance enables population-scale monitoring of antiviral resistance and immune escape-associated mutations and offers a scalable model for broader surveillance.

Indexed as

Antiviral AgentsDrug Resistance, ViralSARS-CoV-2WastewaterCOVID-19Genome, ViralGenomicsHumansMutationOntarioWastewater-Based Epidemiological MonitoringAntiviral AgentsWastewaterantiviral resistanceimmune escapenirmatrelvirpublic health genomicsremdesivirSARS-CoV-2sotrovimabwastewater surveillance

Identifiers

PMID42655739
PMCPMC13517777

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Registered trials

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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.