Evidence map›Paper›PMID 41640304›Full record

ArticleThe Journal of pathology2026

Characterisation of bacteria-induced colitis and its modulation by probiotics in naked mole rats: a new mammalian model for acute inflammatory disease.

Daniel W Hart, Aik Seng Ng, Patrycja Gazińska, Robert Goldin, Purva Gopal, Nicolize O'Dell, Ahmad Zargar, Lior Pytowski, Shamir Montazid, Chiara Bardella and 5 more

Abstract read
In one paragraph

Article in The Journal of pathology, 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

15 authors.

Daniel W HartMammal Research Institute, Department of Zoology and Entomology, University of Pretoria, Pretoria, Republic of South Africa.ORCID https://orcid.org/0000-0002-4592-558X
Aik Seng NgNuffield Department of Clinical Laboratory Sciences, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.ORCID https://orcid.org/0000-0003-1925-4759
Patrycja GazińskaDepartment of Oncology and Haematology, Faculty of Medicine, Wroclaw University of Science and Technology, Wroclaw, Poland.ORCID https://orcid.org/0000-0001-5031-1913
Robert GoldinDepartment of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London, UK.ORCID https://orcid.org/0000-0001-5184-4519
Purva GopalDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.ORCID https://orcid.org/0000-0001-7125-695X
Nicolize O'DellDepartment of Paraclinical Sciences, Faculty of Veterinary Science, University of Pretoria, Pretoria, Republic of South Africa.ORCID https://orcid.org/0000-0003-4793-1948
Ahmad ZargarSchool of Medicine, Worsley Building, University of Leeds, Leeds, UK.ORCID https://orcid.org/0009-0001-2582-7683
Lior PytowskiPixel Biology Ltd., Oxford, UK.ORCID https://orcid.org/0000-0002-8530-5123
Shamir MontazidDepartment of Oncology, University of Oxford, Oxford, UK.ORCID https://orcid.org/0000-0002-4584-5619
Chiara BardellaDepartment of Oncology, University of Oxford, Oxford, UK.ORCID https://orcid.org/0000-0002-7780-2541
James E EastTranslational Gastroenterology and Liver Unit, Nuffield Department of Medicine, Experimental Medicine Division, University of Oxford, John Radcliffe Hospital, Oxford, UK.ORCID https://orcid.org/0000-0001-8035-3700
Ian P TomlinsonDepartment of Oncology, University of Oxford, Oxford, UK.ORCID https://orcid.org/0000-0003-3037-1470
Nadine KochDepartment of Medicine II, University Hospital, LMU Munich, Munich, Germany.ORCID https://orcid.org/0000-0002-3654-0733
Nigel C BennettMammal Research Institute, Department of Zoology and Entomology, University of Pretoria, Pretoria, Republic of South Africa.ORCID https://orcid.org/0000-0001-9748-2947
Shazia IrshadNuffield Department of Clinical Laboratory Sciences, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.ORCID https://orcid.org/0000-0003-4536-373X

Funding

Department of Science and Technology-National Research Foundation DST-NRF (GUN 64756)The National Institute for Health and Care Research (NIHR) Oxford Biomedical Research Centre (BRC)
6 · The paper itself

Abstract

Enteropathogenic bacteria are a major cause of morbidity and mortality globally. While mouse models have been indispensable in advancing our understanding of infectious enteric diseases, key differences in intestinal microbiota and immunobiology between mice and humans underscore the need for alternative mammalian models that better recapitulate human disease states. The naked mole rat (NMR), the longest-lived rodent and a model of healthy ageing, presents a unique opportunity. It possesses an exceptionally robust intestinal barrier, an abundance of goblet cells, a thicker mucin layer, and reduced gut permeability compared to mice. Additionally, the NMR gut microbiome exhibits compositional and functional features shared with human centenarians and traditional-lifestyle populations (e.g. Hadza hunter-gatherers), including an enrichment of health-associated taxa and metabolic pathways. Here, we leverage this model to show that systemic Citrobacter braakii infection is associated with colonic inflammation and epithelial injury that closely mimics human haemorrhagic colitis. Infected NMRs develop mucosal erosions, ulcerations, depletion of goblet cells, expansion of proliferative compartments, and active inflammation in the lamina propria. Without intervention, systemic inflammation associated with sepsis ensues and results in high mortality. Furthermore, we demonstrate the utility of this model for therapeutic testing by showing a strong effect of a probiotic cocktail comprising lactobacilli, bifidobacteria, streptococci, and enterococci. Treatment with this cocktail promoted mucosal healing, restored intestinal homeostasis, and exerted an anti-inflammatory effect. Taken together, we establish the NMR as a translatable model for investigating disease mechanisms in infectious colitis, including disruptions in mucosal barrier permeability, gut microbial ecology, and local and systemic immune regulation, as well as for testing functional probiotic strains as potential therapeutics. © 2026 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

Indexed as

ColitisColonEnterobacteriaceae InfectionsGastrointestinal MicrobiomeProbioticsAcute DiseaseAnimalsDisease Models, AnimalFemaleGoblet CellsIntestinal Barrier FunctionIntestinal MucosaMaleMole RatsCitrobacter braakiiepithelial atypiagoblet cell depletioninfectious colitisinflammationmucosal healingnaked mole ratsprobioticssepsis

Identifiers

PMID41640304
PMCPMC12984493

What OpenQuestion holds

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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.