Evidence map›Paper›PMID 42112377›Full record

ArticleFrontiers in immunology2026

If you give a mouse a poopsicle: a novel fecal microbiota transplant method for exploring the role of the gut microbiome in stress-related outcomes in mice.

Monica A Tschang, Ronin Deo-Campo Vuong, Baylee Eilers, Denise Chac, Adam Waalkes, Kelsi Penewit, Alyssa Easton, Bryan Schuessler, Renata Daniels, Ana A Weil and 3 more

Abstract read
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Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

13 authors.

Monica A TschangGraduate Program in Neuroscience, University of Washington, Seattle, WA, United States.
Ronin Deo-Campo VuongCenter for the Neurobiology of Addiction, Pain, & Emotion, University of Washington, Seattle, WA, United States.
Baylee EilersGeriatric Research Education and Clinical Center, Veterans Affairs Puget Sound, Seattle, WA, United States.
Denise ChacDepartment of Medicine, University of Washington, Seattle, WA, United States.
Adam WaalkesDepartment of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA, United States.
Kelsi PenewitDepartment of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA, United States.
Alyssa EastonGraduate Program in Molecular Engineering, University of Washington, Seattle, WA, United States.
Bryan SchuesslerGeriatric Research Education and Clinical Center, Veterans Affairs Puget Sound, Seattle, WA, United States.
Renata DanielsGeriatric Research Education and Clinical Center, Veterans Affairs Puget Sound, Seattle, WA, United States.
Ana A WeilDepartment of Medicine, University of Washington, Seattle, WA, United States.
Stephen J SalipanteDepartment of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA, United States.
Sean M GibbonsGraduate Program in Molecular Engineering, University of Washington, Seattle, WA, United States.
Abigail G SchindlerGraduate Program in Neuroscience, University of Washington, Seattle, WA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The microbiome-gut-brain axis is a mediator of stress-related disorders. The number of preclinical studies exploring the potential causal mechanism of this connection using fecal microbiota transplantation (FMT) is growing. However, the most common method for delivering fecal transplants in rodent models is still oral gavage, which creates an adverse experience that may confound stress-related outcomes. Here, we establish an alternative methodology for FMT that decreases stress induced by traditional experimental procedures. Methods: We first used preference and anxiety behavior assays to identify antibiotic therapies having maximal tolerability and minimal anxiolytic properties. We then collected feces from donor mice and homogenized them with a microbe-stabilizing buffer to create a slurry, which was frozen into aliquots ("poopsicles") for subsequent FMT. Recipient mice voluntarily consumed the frozen aliquots, and blood was collected to compare corticosterone relative to that after delivery via traditional gavage. Results: Plasma corticosterone levels were found to be significantly lower in mice receiving frozen aliquots compared to oral gavage. Furthermore, relative to controls, microbial signatures of mice receiving FMT via frozen aliquots were more similar to those of the donors at one week following final FMT and were sustained for up to six weeks, as assessed by comparing Bray-Curtis beta diversity distances. Conclusion: Together, these results establish antibiotic and FMT methods that minimize treatment-induced stress, while effectively transplanting fecal microbes between murine conspecifics.

Indexed as

AnxietyFecal Microbiota TransplantationGastrointestinal MicrobiomeStress, PsychologicalAnimalsCorticosteroneDisease Models, AnimalFecesMaleMiceMice, Inbred C57BLCorticosterone16S sequencingfecal microbiota transplant (FMT)microbiomemouseoral gavagepoopsicleself-administrationstress

Identifiers

PMID42112377
PMCPMC13152772

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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.