Evidence map›Paper›PMID 42367871›Full record

ArticlebioRxiv : the preprint server for biology2026

A gavage-fomite based method to generate mouse models with natural microbiota.

Geongoo Han, Mohammad H Hasan, Olumide Adesioye, Jessica Pacia, Julian C Ramprashad, Gregorio Valdez, Shipra Vaishnava, Lalit K Beura

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

5 · Who and what money

Authors and funding

8 authors.

Geongoo HanDepartment of Molecular Microbiology and Immunology, Brown University, Providence, RI, 02912.
Mohammad H HasanDepartment of Molecular Microbiology and Immunology, Brown University, Providence, RI, 02912.
Olumide AdesioyeDepartment of Molecular Microbiology and Immunology, Brown University, Providence, RI, 02912.
Jessica PaciaDepartment of Molecular Microbiology and Immunology, Brown University, Providence, RI, 02912.
Julian C RamprashadDepartment of Molecular Microbiology and Immunology, Brown University, Providence, RI, 02912.
Gregorio ValdezDepartment of Molecular Biology, Cell Biology and Biochemistry, Brown University, Providence, RI, 02912.
Shipra VaishnavaDepartment of Molecular Microbiology and Immunology, Brown University, Providence, RI, 02912.
Lalit K BeuraDepartment of Molecular Microbiology and Immunology, Brown University, Providence, RI, 02912.

Funding

T lymphocyte-mediated protection of the reproductive mucosaR01AI177704 · NIAID · BROWN UNIVERSITY · PI Lalit K Beura · 2024 to 2026
$2.0M
Development of a microbial-rich exposure regimen to accelerate translational research using mouse models of Alzheimer's Disease to humans.R21AG079550 · NIA · BROWN UNIVERSITY · PI VALDEZ, GREGORIO · 2023 to 2024
$439k
NIAID NIH HHS R01 AI177704NIA NIH HHS R21 AG079550
6 · The paper itself

Abstract

Laboratory-raised specific pathogen-free (SPF) mice have been indispensable for fundamental immunology research, yet their reliability in predicting human clinical outcomes has been questionable. A major factor contributing to this disconnect is the sanitized housing environment, which deprives laboratory mice of physiological microbial exposure critical for immune maturation. Various approaches have been developed to introduce microbes to SPF mice, aiming to mimic human-like microbial experiences and engender adult human-like immune traits. However, some of these methods, specifically the pet store mice cohousing approach suffer from significant variability in pathogen exposure driven by the uncontrolled nature of microbial exchange and is associated with heightened mortality. Here we present an alternative gavage-fomite (GaF) method that exposes mice to a similarly diverse array of pathogens and commensal as the pet store cohousing method while limiting mortality. GaF-treated mice exhibited consistent gut microbial composition, robust immune maturation characterized by mucosal T-cell distribution, elevated serum inflammatory cytokines, and a splenic immune transcriptional signature closely aligned with that of adult humans. Furthermore, these mice demonstrated enhanced protection against a virulent bacterial challenge. The simplicity, and effectiveness of the GaF method for generating 'mice with natural microbiota,' may support broader use of these models in basic and translational immunological research across institutions.

Indexed as

Antigen-experienced CD8 T cellsImmune maturationMicrobial exposureMouse models with natural microbiota

Identifiers

PMID42367871
PMCPMC13308046

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.