Evidence map›Paper›PMID 41757041›Full record

ArticlebioRxiv : the preprint server for biology2026

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 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

13 authors.

Monica A TschangGraduate Program in Neuroscience, University of Washington, Seattle, WA, USA.ORCID 0009-0003-0721-6680
Ronin Deo-Campo VuongCenter for the Neurobiology of Addiction, Pain, & Emotion, Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA.
Baylee EilersGeriatric Research Education and Clinical Center, Veterans Affairs Puget Sound, Seattle, WA, USA.
Denise ChacDepartment of Medicine, University of Washington, Seattle, WA, USA.ORCID 0000-0002-4183-3899
Adam WaalkesDepartment of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA, USA.
Kelsi PenewitDepartment of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA, USA.
Alyssa EastonGraduate Program in Molecular Engineering, University of Washington, Seattle, WA, USA.
Bryan SchuesslerGeriatric Research Education and Clinical Center, Veterans Affairs Puget Sound, Seattle, WA, USA.
Renata DanielsGeriatric Research Education and Clinical Center, Veterans Affairs Puget Sound, Seattle, WA, USA.
Ana A WeilDepartment of Medicine, University of Washington, Seattle, WA, USA.ORCID 0000-0002-6170-4306
Stephen J SalipanteDepartment of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA, USA.
Sean M GibbonsGraduate Program in Molecular Engineering, University of Washington, Seattle, WA, USA.ORCID 0000-0002-8724-7916
Abigail G SchindlerGraduate Program in Neuroscience, University of Washington, Seattle, WA, USA.ORCID 0000-0002-7039-1348

Funding

University of Washington Center of Excellence in Opioid Addiction ResearchP30DA048736 · NIDA · UNIVERSITY OF WASHINGTON · PI Charles Chavkin · 2019 to 2026
$13.0M
TRAINING IN THE MOLECULAR PHARMACOLOGY OF ABUSED DRUGST32DA007278 · NIDA · UNIVERSITY OF WASHINGTON · PI Susan Marie Ferguson, Paul E. M. Phillips · 1993 to 2026
$9.8M
NIDA NIH HHS P30 DA048736NIDA NIH HHS T32 DA007278
6 · The paper itself

Abstract

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. 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 pellets ("poopsicles") for subsequent FMT. Recipient mice voluntarily consumed the pellets, and blood was collected to compare corticosterone levels relative to traditional gavage FMT. Plasma corticosterone levels were found to be significantly lower in mice receiving FMT via pellets compared to oral gavage. Furthermore, relative to gavage FMT, microbial signatures of mice receiving FMT via pellets were more similar to those of the donor pellets at one week following final FMT and were sustained for up to six weeks, as assessed by comparing Bray-Curtis beta-diversity distances. Together, these results establish effective antibiotic and FMT methods that minimize treatment-induced stress, while effectively transplanting fecal microbes between murine conspecifics.

Indexed as

16S sequencingfecal microbiota transplant (FMT)microbiomemouseoral gavagepoopsicleself-administrationstress

Identifiers

PMID41757041
PMCPMC12934603

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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.