Evidence map›Paper›PMID 41932893›Full record

ArticleNature communications2026

Complex temporal dynamics of phage-bacteria populations in an animal-associated marine system.

Jeffrey Liang, Karine Cahier, Damien Piel, Dario Cueva Granda, David Goudenège, Yannick Labreuche, Laurence Ma, Marc Monot, Charles Bernard, Eduardo P C Rocha and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. The Zoetrope effect in phage evolution.Frontiers in microbiology · 2026
    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

11 authors.

Jeffrey Liang *Département de microbiologie, infectiologie et immunologie & Institut Courtois d'innovation biomedicale, Université de Montréal, Montréal, QC, Canada.
Karine Cahier *Sorbonne Université, CNRS, UMR 8227, Integrative Biology of Marine Models, Station Biologique de Roscoff, Roscoff cedex, France.
Damien PielSorbonne Université, CNRS, UMR 8227, Integrative Biology of Marine Models, Station Biologique de Roscoff, Roscoff cedex, France.ORCID http://orcid.org/0009-0006-3760-8142
Dario Cueva GrandaDépartement de microbiologie, infectiologie et immunologie & Institut Courtois d'innovation biomedicale, Université de Montréal, Montréal, QC, Canada.
David GoudenègeSorbonne Université, CNRS, UMR 8227, Integrative Biology of Marine Models, Station Biologique de Roscoff, Roscoff cedex, France.
Yannick LabreucheSorbonne Université, CNRS, UMR 8227, Integrative Biology of Marine Models, Station Biologique de Roscoff, Roscoff cedex, France.
Laurence MaInstitut Pasteur, Université Paris Cité, Plate-forme Technologique Biomics, Paris, France.
Marc MonotInstitut Pasteur, Université Paris Cité, Plate-forme Technologique Biomics, Paris, France.ORCID http://orcid.org/0000-0003-0738-7335
Charles BernardInstitut Pasteur, Université Paris Cité, CNRS UMR3525, Microbial Evolutionary Genomics, Paris, France.
Eduardo P C RochaInstitut Pasteur, Université Paris Cité, CNRS UMR3525, Microbial Evolutionary Genomics, Paris, France. eduardo.rocha@pasteur.fr.ORCID http://orcid.org/0000-0001-7704-822X
Frédérique Le RouxDépartement de microbiologie, infectiologie et immunologie & Institut Courtois d'innovation biomedicale, Université de Montréal, Montréal, QC, Canada. frederique.le.roux@umontreal.ca.ORCID http://orcid.org/0000-0002-9112-6199

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-20-CE35-0014Canada Excellence Research Chairs, Government of Canada (Canada Excellence Research Chairs Program) 2022-00051EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 884988Fonds de Recherche du Québec-Société et Culture (FRQSC) 44584
6 · The paper itself

Abstract

Bacteriophages-bacteria interactions drive rapid evolution of both partners in laboratory studies. To understand how these dynamics unfold in natural environments, we re-sampled a population of Vibrio crassostreae and their phages in an open, animal-associated marine system four years apart. Analysis of over 1000 predominantly virulent phages revealed rapid change of some lineages, but persistence of others, with genomes highly conserved between years. This pattern is consistent with low substitution rates in persistent lineages and may reflect phages overwintering in wild oysters, slow virion decay, and for temperate phages, lysogeny within hosts. Over 600 V. crassostreae strains recovered at both time points assorted into the same major clades. Oyster-associated vibrios have larger genomes and more abundant and diverse mobile genetic elements suggesting that oysters are hotspots for genetic exchange and horizontal gene transfer. Their genomes encode virulence plasmids, prophages carrying anti-phage systems, phage-plasmids, and phage satellites that persist intracellularly as plasmids. Time series analyses revealed weak correlations between phage and bacterial abundances, a pattern compatible with cryptic population dynamics arising from genetic diversity. Together, these results indicate that natural coevolving phage-bacteria populations can exhibit complex dynamics, with rapid replacement of some lineages alongside multi-year persistence of others.

Indexed as

BacteriophagesOstreidaeVibrioAnimalsGenetic VariationGene Transfer, HorizontalGenome, ViralLysogenyPhylogenyProphages

Identifiers

PMID41932893
PMCPMC13230959

What OpenQuestion holds

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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.