Evidence map›Paper›PMID 40770182›Full record

ArticleNature communications2025

Using COVID-19 pandemic perturbation to model RSV-hMPV interactions and potential implications under RSV interventions.

Emily Howerton, Thomas C Williams, Jean-Sébastien Casalegno, Samuel Dominguez, Rory Gunson, Kevin Messacar, C Jessica E Metcalf, Sang Woo Park, Cécile Viboud, Bryan T Grenfell

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Complex multiannual cycles ofProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. Article
  8. Review
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.

Emily HowertonDepartment of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ, USA. ehowerton@princeton.edu.ORCID http://orcid.org/0000-0002-0639-3728
Thomas C WilliamsChild Life and Health, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0002-3866-1344
Jean-Sébastien CasalegnoHospices Civils de Lyon, Hôpital de la Croix-Rousse, Centre de Biologie Nord, Institut des Agents Infectieux, Laboratoire de Virologie, Lyon, France.ORCID http://orcid.org/0000-0003-3271-9856
Samuel DominguezDepartment of Pediatrics, Section of Infectious Diseases, University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, CO, USA.
Rory GunsonWest of Scotland Specialist Virology Centre, NHS Greater Glasgow and Clyde, Glasgow, UK.
Kevin MessacarDepartment of Pediatrics, Section of Infectious Diseases, University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, CO, USA.ORCID http://orcid.org/0000-0001-5830-3491
C Jessica E MetcalfDepartment of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ, USA.
Sang Woo ParkDepartment of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ, USA.ORCID http://orcid.org/0000-0003-2202-3361
Cécile ViboudFogarty International Center, National Institutes of Health, Bethesda, MD, USA.ORCID http://orcid.org/0000-0003-3243-4711
Bryan T GrenfellDepartment of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ, USA.ORCID http://orcid.org/0000-0003-3227-5909

Funding

WORK ORDER 126643 B539 EXPAND IC SUITE75N91019D00024 · NIAID · LEIDOS BIOMEDICAL RESEARCH, INC. · PI BRISCOE, LYNN · 2019 to 2025
$3932.6M
NCI NIH HHS 75N91019D00024U.S. Department of Health & Human Services | National Institutes of Health (NIH) Prime Contract No. 75N91019D00024, Task Order No. 75N91023F00016
6 · The paper itself

Abstract

Respiratory syncytial virus (RSV) and human metapneumovirus (hMPV) are closely related pathogens responsible for a significant burden of acute respiratory infections. Interactions between RSV and hMPV have been hypothesized, but the mechanisms of interaction are largely unknown. Here, we use a mathematical model to quantify the likelihood of interactions from population-level surveillance data and investigate whether interactions could lead to increases in hMPV burden under RSV medical interventions, including active and passive immunization. In Scotland, Korea, and three regions of Canada, annual hMPV outbreaks lag RSV outbreaks by up to 18 weeks; two Canadian regions show patterns consistent with out-of-phase biennial outbreaks. Using a two-pathogen transmission model, we show that a negative effect of RSV infection on hMPV transmissibility can explain these dynamics. We use post-pandemic RSV-hMPV rebound dynamics as an out of sample test for our model, and the model with interactions better predicts this period than a model where the pathogens are assumed to be independent. Finally, our model suggests that hMPV peak timing and magnitude may change under RSV interventions. Our analysis provides a foundation for detecting possible RSV-hMPV interactions at the population level, although such a model oversimplifies important complexities about interaction mechanisms.

Indexed as

COVID-19MetapneumovirusParamyxoviridae InfectionsRespiratory Syncytial Virus, HumanRespiratory Syncytial Virus InfectionsCanadaHumansModels, BiologicalModels, TheoreticalPandemicsRepublic of KoreaSARS-CoV-2Scotland

Identifiers

PMID40770182
PMCPMC12328645

What OpenQuestion holds

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LicenceCC BY
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.