Evidence map›Paper›PMID 40065807›Full record

ArticleDiscovery immunology2025

Comparison of naturalization mouse model setups uncover distinct effects on intestinal mucosa depending on microbial experience.

Henriette Arnesen, Signe Birkeland, Harriet Stendahl, Klaus Neuhaus, David Masopust, Preben Boysen, Harald Carlsen

Abstract read
In one paragraph

Article in Discovery immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

7 authors.

Henriette ArnesenDepartment of Preclinical Science and Pathology, Faculty of Veterinary Medicine, Norwegian University of Life Sciences (NMBU), Ås, Norway.ORCID https://orcid.org/0000-0003-1173-4010
Signe BirkelandFaculty of Chemistry, Biotechnology and Food Science, Norwegian University of Life Sciences (NMBU), Ås, Norway.ORCID https://orcid.org/0009-0008-5018-9741
Harriet StendahlDepartment of Preclinical Science and Pathology, Faculty of Veterinary Medicine, Norwegian University of Life Sciences (NMBU), Ås, Norway.
Klaus NeuhausCore Facility Microbiome, ZIEL - Institute for Food & Health, Technische Universität München (TUM), Freising, Germany.
David MasopustCenter for Immunology, Department of Microbiology and Immunology, University of Minnesota (UMN), Minneapolis, MN, USA.
Preben BoysenDepartment of Preclinical Science and Pathology, Faculty of Veterinary Medicine, Norwegian University of Life Sciences (NMBU), Ås, Norway.
Harald CarlsenFaculty of Chemistry, Biotechnology and Food Science, Norwegian University of Life Sciences (NMBU), Ås, Norway.ORCID https://orcid.org/0000-0001-5123-5756

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Concerns regarding the translational value of preclinical mouse models have been addressed by introducing various approaches of 'naturalizing' research mice, which provide them with more diverse microbiomes and physiological immune responses. We have previously shown that 'feralized' mice, that is, inbred laboratory mice raised in a farmyard-like, microbe-rich environment exhibit a shifted gut microbiota, matured immunophenotype, and reduced severity of colorectal cancer. Similar studies occasionally involve co-housing with wild or pet-store-raised mice as microbial donors integrating species-specific commensals and pathogens. To what extent these different practices of microbial exposure are crucial for the resulting mouse phenotype remains unclear. Methods: Here, we present the first side-by-side comparison of different methods to naturalize laboratory mice: co-housing with wild-caught house mice, feralization in a farmyard-like habitat only, or a combination of the two, with conventional clean laboratory mice as a reference. Results: Independent of the method, the naturalized colon-mucosa microbiota, was colonized by several Conclusion: These findings enhance our understanding of naturalization model setups and effects on the gut barrier and immune system, thereby aiding future decisions on the utilization of naturalized mouse models.

Indexed as

feralized micegut microbiotaintestinal mucosamemory T cellsnaturalized mice

Identifiers

PMID40065807
PMCPMC11892432

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.