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Colitis reduces active social engagement in mice and is ameliorated by supplementation with human microbiota members

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  • D. Garrett Brown

    (University of Utah School of Medicine, Huntsman Cancer Institute, Division of Microbiology and Immunology)

  • Michaela Murphy

    (University of Utah School of Medicine, Huntsman Cancer Institute, Division of Microbiology and Immunology)

  • Roberto Cadeddu

    (Department of Pharmacology and Toxicology University of Utah College of Pharmacy)

  • Rickesha Bell

    (University of Utah School of Medicine, Huntsman Cancer Institute, Division of Microbiology and Immunology)

  • Allison Weis

    (University of Utah School of Medicine, Huntsman Cancer Institute, Division of Microbiology and Immunology)

  • Tyson Chiaro

    (University of Utah School of Medicine, Huntsman Cancer Institute, Division of Microbiology and Immunology)

  • Kendra Klag

    (University of Utah School of Medicine, Huntsman Cancer Institute, Division of Microbiology and Immunology)

  • Jubel Morgan

    (University of Utah School of Medicine)

  • Hilary Coon

    (University of Utah School of Medicine)

  • W. Zac Stephens

    (University of Utah School of Medicine, Huntsman Cancer Institute, Division of Microbiology and Immunology)

  • Marco Bortolato

    (Department of Pharmacology and Toxicology University of Utah College of Pharmacy)

  • June L. Round

    (University of Utah School of Medicine, Huntsman Cancer Institute, Division of Microbiology and Immunology)

Abstract

Multiple neurological disorders are associated with gastrointestinal (GI) symptoms, including autism spectrum disorder (ASD). However, it is unclear whether GI distress itself can modify aspects of behavior. Here, we show that mice that experience repeated colitis have impaired active social engagement, as measured by interactions with a foreign mouse, even though signs of colitis were no longer present. We then tested the hypothesis that individuals with ASD harbor a microbiota that might differentially influence GI health by performing microbiota transplantation studies into male germfree animals, followed by induction of colitis. Animals that harbor a microbiota from ASD individuals have worsened gut phenotypes when compared to animals colonized with microbiotas from familial neurotypical (NT) controls. We identify the enrichment of Blautia species in all familial NT controls and observe an association between elevated abundance of Bacteroides uniformis and reductions in intestinal injury. Oral treatment with either of these microbes reduces colon injury in mice. Finally, provision of a Blautia isolate from a NT control ameliorates gut injury-associated active social engagement in mice. Collectively, our data demonstrate that past intestinal distress is associated with changes in active social behavior in mice that can be ameliorated by supplementation of members of the human microbiota.

Suggested Citation

  • D. Garrett Brown & Michaela Murphy & Roberto Cadeddu & Rickesha Bell & Allison Weis & Tyson Chiaro & Kendra Klag & Jubel Morgan & Hilary Coon & W. Zac Stephens & Marco Bortolato & June L. Round, 2024. "Colitis reduces active social engagement in mice and is ameliorated by supplementation with human microbiota members," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-46733-7
    DOI: 10.1038/s41467-024-46733-7
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    References listed on IDEAS

    as
    1. You Yu & Bing Zhang & Peifeng Ji & Zhenqiang Zuo & Yongxi Huang & Ning Wang & Chang Liu & Shuang-Jiang Liu & Fangqing Zhao, 2022. "Changes to gut amino acid transporters and microbiome associated with increased E/I ratio in Chd8+/− mouse model of ASD-like behavior," Nature Communications, Nature, vol. 13(1), pages 1-15, December.
    2. Sarkis K. Mazmanian & June L. Round & Dennis L. Kasper, 2008. "A microbial symbiosis factor prevents intestinal inflammatory disease," Nature, Nature, vol. 453(7195), pages 620-625, May.
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