Evidence map›Paper›PMID 40036582›Full record

ArticleThe ISME journal2025

Mice expressing the autism-associated neuroligin-3 R451C variant exhibit increased mucus density and altered distributions of intestinal microbiota.

Madushani Herath, Joel C Bornstein, Elisa L Hill-Yardin, Ashley E Franks

Abstract read
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Article in The ISME journal, 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

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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

4 citing papers in PubMed.

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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

4 authors.

Madushani HerathDepartment of Anatomy and Physiology, University of Melbourne, Grattan Street, Parkville, Victoria 3010, Australia.
Joel C BornsteinDepartment of Anatomy and Physiology, University of Melbourne, Grattan Street, Parkville, Victoria 3010, Australia.
Elisa L Hill-YardinDepartment of Anatomy and Physiology, University of Melbourne, Grattan Street, Parkville, Victoria 3010, Australia.
Ashley E FranksDepartment of Microbiology, Anatomy Physiology and Pharmacology, School of Agriculture, Biomedicine and Environment, La Trobe University, Plenty Road, Bundoora, Victoria 3086, Australia.ORCID 0000-0003-1664-6060

Funding

Australian Research Council Future Fellowship FT160100126RMIT Vice Chancellor's Senior Research Fellowship APP1158952
6 · The paper itself

Abstract

The intestinal mucus layer protects the host from invading pathogens and is essential for maintaining a healthy mucosal microbial community. Alterations in the mucus layer and composition of mucus-residing microbiota in people diagnosed with autism may contribute to dysbiosis and gastrointestinal dysfunction. Although microbial dysbiosis based on sequencing data is frequently reported in autism, spatial profiling of microbes adjacent to the mucosa is needed to identify changes in bacterial subtypes in close contact with host tissues. Here, we analysed the spatial distribution of the mucin-2 protein using immunofluorescence as well as total bacteria, Bacteroidetes, Firmicutes phyla, and Akkermansia muciniphila using fluorescent in situ hybridization in mice expressing the autism-associated R451C variant in the Neuroligin-3 gene. We show that the Neuroligin-3 R451C variant increases mucus density adjacent to the distal ileal epithelium in mice. The relative density of total bacteria, Firmicutes, and A. muciniphila was increased whereas the density of Bacteroidetes was decreased closer to the epithelium in Neuroligin-3R451C mice. In summary, the autism-associated R451C variant in the Neuroligin-3 gene increases mucus density adjacent to the epithelium and alters microbial spatial distribution in the mouse distal ileum.

Indexed as

Autistic DisorderCell Adhesion Molecules, NeuronalGastrointestinal MicrobiomeIntestinal MucosaMembrane ProteinsMucusNerve Tissue ProteinsAkkermansiaAnimalsBacillotaBacteroidetesDysbiosisIleumIn Situ Hybridization, FluorescenceMaleMiceCell Adhesion Molecules, NeuronalMembrane ProteinsMuc2 protein, mouseMucin-2Nerve Tissue Proteinsneuroligin 3autism spectrum disordermicrobial dysbiosismucus layerneuroligin-3spatial distribution of bacteria

Identifiers

PMID40036582
PMCPMC11954627

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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.