Evidence map›Paper›PMID 40730751›Full record

ArticleNature communications2025

Maternal emulsifier consumption alters the offspring early-life microbiota and goblet cell function leading to long-lasting diseases susceptibility.

Clara Delaroque, Héloïse Rytter, Erica Bonazzi, Marine Huillet, Sandrine Ellero-Simatos, Eva Chatonnat, Fuhua Hao, Andrew Patterson, Benoit Chassaing

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
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  3. Follow the microbes: a new perspective on health inequalities.The British journal of general practice : the journal of the Royal College of General Practitioners · 2026
    Article
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  5. Review
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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

9 authors.

Clara DelaroqueMicrobiome-Host Interactions, Institut Pasteur, Université Paris Cité, INSERM U1306, Paris, France.
Héloïse RytterMicrobiome-Host Interactions, Institut Pasteur, Université Paris Cité, INSERM U1306, Paris, France.
Erica BonazziMicrobiome-Host Interactions, Institut Pasteur, Université Paris Cité, INSERM U1306, Paris, France.
Marine HuilletToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de Toulouse, Toulouse, France.
Sandrine Ellero-SimatosToxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UPS, Université de Toulouse, Toulouse, France.ORCID http://orcid.org/0000-0002-9282-1804
Eva ChatonnatMicrobiome-Host Interactions, Institut Pasteur, Université Paris Cité, INSERM U1306, Paris, France.
Fuhua HaoDepartment of Veterinary and Biomedical Sciences, Center for Molecular Toxicology and Carcinogenesis, Pennsylvania State University, University Park, PA, USA.
Andrew PattersonDepartment of Veterinary and Biomedical Sciences, Center for Molecular Toxicology and Carcinogenesis, Pennsylvania State University, University Park, PA, USA.ORCID http://orcid.org/0000-0003-2073-0070
Benoit ChassaingMicrobiome-Host Interactions, Institut Pasteur, Université Paris Cité, INSERM U1306, Paris, France. benoit.chassaing@pasteur.fr.ORCID http://orcid.org/0000-0002-4285-769X

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-20-PAMR-0002Agence Nationale de la Recherche (French National Research Agency) ANR-21-CE15-0042-01Agence Nationale de la Recherche (French National Research Agency) ANR-24-PESA-008EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) ERC-2018-StG-804135EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) ERC-2024-CoG-101170920
6 · The paper itself

Abstract

Early-life acquisition of microbiota and, consequently, immune system development, both lastingly impacts health. Accordingly, we hypothesized that disturbing the microbiota of lactating mothers via consumption of dietary emulsifiers might alter the microbiota, and perhaps the immune system, of their offspring, thereby increasing susceptibility to microbiota-mediated diseases, including colitis and metabolic syndrome. Here we report that, in mice, maternal consumption of carboxymethylcellulose and polysorbate-80 resulted in transient alterations in offspring microbiotas that were necessary and sufficient to increase proneness to colitis and metabolic syndrome in young adulthood. Offspring microbiome alterations induced by maternal emulsifier consumption resulted in elevated levels of pro-inflammatory flagellin, bacterial encroachment, and premature closure of goblet cell associated antigens passages (GAPs). The latter event was linked to phenotypic outcome in that pharmacologically preventing GAP closure eliminated the detrimental of maternal emulsifier consumption. Collectively, these results illustrate the potential of dietary emulsifiers to drive transgenerational microbiota alteration and, consequently, hastened immune development that increases susceptibility to inflammatory diseases.

Indexed as

Emulsifying AgentsGastrointestinal MicrobiomeGoblet CellsMicrobiotaPrenatal Exposure Delayed EffectsAnimalsCarboxymethylcellulose SodiumColitisDisease SusceptibilityFemaleMaleMetabolic SyndromeMiceMice, Inbred C57BLPolysorbatesPregnancyCarboxymethylcellulose SodiumEmulsifying AgentsPolysorbates

Identifiers

PMID40730751
PMCPMC12307616

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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.