Evidence map›Paper›PMID 41673237›Full record

ArticleScientific reports2026

Microbiological and rheological dynamics of mixed biofilms formed by bacteria and eukaryotic virus.

Jing Gao, Clémence Abriat, Magdalena Laekas-Hameder, Nick Virgilio, Charles M Dozois, Caroline Quach, Marie-Claude Heuzey, Guy Lemay, France Daigle

Abstract read
In one paragraph

Article in Scientific reports, 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. 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

9 authors.

Jing GaoDepartment of Microbiology, Infectious Diseases and Immunology, Université de Montréal, Montreal, Québec, Canada.
Clémence AbriatDepartment of Microbiology, Infectious Diseases and Immunology, Université de Montréal, Montreal, Québec, Canada.
Magdalena Laekas-HamederDepartment of Microbiology, Infectious Diseases and Immunology, Université de Montréal, Montreal, Québec, Canada.
Nick VirgilioDepartment of Chemical Engineering, CREPEC, Polytechnique Montréal, Montréal, Québec, Canada.
Charles M DozoisFaculty of Veterinary Medicine, CRIPA, Swine and Poultry Infectious Diseases Research Center, University of Montreal, St-Hyacinthe, Québec, Canada.
Caroline QuachDepartment of Microbiology, Infectious Diseases and Immunology, Université de Montréal, Montreal, Québec, Canada.
Marie-Claude HeuzeyDepartment of Chemical Engineering, CREPEC, Polytechnique Montréal, Montréal, Québec, Canada.
Guy LemayDepartment of Microbiology, Infectious Diseases and Immunology, Université de Montréal, Montreal, Québec, Canada.
France DaigleDepartment of Microbiology, Infectious Diseases and Immunology, Université de Montréal, Montreal, Québec, Canada. france.daigle@umontreal.ca.ORCID http://orcid.org/0000-0001-6847-4729

Funding

New Frontiers in Research NFRFE-2022-00464
6 · The paper itself

Abstract

Biofilms are structured microbial communities embedded within an extracellular matrix that confers protection against environmental stresses. In both natural and clinical settings, biofilms are rarely composed of a single species and may also involve interactions with bacteriophages or even eukaryotic viruses. Since both biofilms and viruses are ubiquitous, and viruses remain among the neglected components of the microbiome, understanding their interactions is essential. In hospitalized patients, catheter colonization by biofilms markedly increases the risk of bacteremia and septicemia, and biofilm formation is almost inevitable during long-term catheterization. In this study, we investigated biofilm-forming capacities of uropathogenic Escherichia coli (UPEC) and clinical strains associated with catheter-related systemic infections. Selected strains were further examined to evaluate the influence of the ubiquitous mammalian reovirus on bacterial biofilm formation and to evaluate biofilm entrapment of viral particles and its impact on viral infectivity. Bacterial growth, survival and biofilm production were measured in the presence or absence of the virus. While reovirus exhibited no bactericidal effects and biofilm biomass remained largely unchanged, rheological and microscopic analyses revealed strain-specific alterations in biofilm properties. Remarkably, reovirus retains infectivity after release from biofilms, indicating that bacterial biofilms may serve as reservoirs or shelters for eukaryotic viruses.

Indexed as

BiofilmsUropathogenic Escherichia coliHumansRheologyBacteriaBiofilmBulk rheologyEscherichia coliReovirusVirus-bacteria

Identifiers

PMID41673237
PMCPMC12966499

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.