Evidence map›Paper›PMID 42531353›Full record

ArticlePLoS biology2026

Viruses help shape microbiome response to polyphenol rewiring of methane-suppressed peat microcosms.

James Riddell V, Rokaiya Nurani Shatadru, Garrett J Smith, Bridget B McGivern, Jared B Ellenbogen, Sophie K Jurgensen, Ami Fofana, Malak M Tfaily, Kelly C Wrighton, Matthew B Sullivan

Abstract read
In one paragraph

Article in PLoS biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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.

James Riddell VDepartment of Microbiology, The Ohio State University, Columbus, Ohio, United States of America.ORCID https://orcid.org/0000-0001-5052-4513
Rokaiya Nurani ShatadruDepartment of Microbiology, The Ohio State University, Columbus, Ohio, United States of America.
Garrett J SmithEMERGE Biology Integration Institute, The Ohio State University, Columbus, Ohio, United States of America.
Bridget B McGivernEMERGE Biology Integration Institute, The Ohio State University, Columbus, Ohio, United States of America.
Jared B EllenbogenEMERGE Biology Integration Institute, The Ohio State University, Columbus, Ohio, United States of America.
Sophie K JurgensenEMERGE Biology Integration Institute, The Ohio State University, Columbus, Ohio, United States of America.
Ami FofanaDepartment of Microbiology, The Ohio State University, Columbus, Ohio, United States of America.
Malak M TfailyEMERGE Biology Integration Institute, The Ohio State University, Columbus, Ohio, United States of America.
Kelly C WrightonEMERGE Biology Integration Institute, The Ohio State University, Columbus, Ohio, United States of America.
Matthew B SullivanDepartment of Microbiology, The Ohio State University, Columbus, Ohio, United States of America.ORCID https://orcid.org/0000-0001-8398-8234

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human activities are accelerating permafrost thaw and subsequent methane emissions from increased microbial activity, prompting microbiome engineering efforts as an emissions mitigation strategy. We recently demonstrated that catechin amendment could drastically reduce methane emissions (>80%) in peat microcosms by enriching catechin-degrading prokaryotes that outcompeted methanogens for hydrogen. However, viral contributions to such microbiome-level responses remain unexplored and we hypothesized that viral dynamics could help shape the microbiome response as nutrient amendments may alter cellular physiology in ways that could induce lytic viral activity. Here, we performed virus eco-genomics analyses of the previously-studied time-resolved multi-omics data collected from catechin-amended peat microcosms. We conservatively identified 900 putatively lytic viral operational taxonomic units (vOTUs), with 41% predicted to infect active host genomes including the most transcriptionally active vOTUs predicted to infect key catechin-degrading genera (Clostridium and undescribed Bacillota JAGFXR01). Notably, a single JAGFXR01-targeting vOTU dominating the viral response (>40% of community viral transcription; 20-156-fold more abundant than its host), which we interpreted as induction resulting in intense lytic activity that could release catechin degradation intermediates to other community members. Consistent with this, gene expression analysis revealed elevated catechin-intermediate degradation and hydrogenase signals in 34 additional polyphenol-degrading metagenome-assembled genomes. These findings support a model consistent with a viral shunt-like process that extends our previous prokaryote-centric model: viral lysis of fast-growing catechin degraders redistributes phenolic intermediates to diverse phenol-degrading taxa that sustain methane suppression via hydrogen consumption. Beyond carbon cycling importance in this system, elucidating unintended virus-mediated responses to nutrient and prebiotic interventions will enable more predictable and effective microbiome engineering strategies across soil, ocean, and human ecosystems.

Indexed as

MethaneMicrobiotaPolyphenolsSoil MicrobiologySoilMethanePolyphenolsSoil

Identifiers

PMID42531353
PMCPMC13460747

What OpenQuestion holds

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LicenceCC BY
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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.