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The microbiota promotes social behavior by modulating microglial remodeling of forebrain neurons

Host-associated microbiotas guide the trajectory of developmental programs, and altered microbiota composition is linked to neurodevelopmental conditions such as autism spectrum disorder. Recent work suggests that microbiotas modulate behavioral phenotypes associated with these disorders. We discove...

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Autores principales: Bruckner, Joseph J., Stednitz, Sarah J., Grice, Max Z., Zaidan, Dana, Massaquoi, Michelle S., Larsch, Johannes, Tallafuss, Alexandra, Guillemin, Karen, Washbourne, Philip, Eisen, Judith S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9624426/
https://www.ncbi.nlm.nih.gov/pubmed/36318534
http://dx.doi.org/10.1371/journal.pbio.3001838
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author Bruckner, Joseph J.
Stednitz, Sarah J.
Grice, Max Z.
Zaidan, Dana
Massaquoi, Michelle S.
Larsch, Johannes
Tallafuss, Alexandra
Guillemin, Karen
Washbourne, Philip
Eisen, Judith S.
author_facet Bruckner, Joseph J.
Stednitz, Sarah J.
Grice, Max Z.
Zaidan, Dana
Massaquoi, Michelle S.
Larsch, Johannes
Tallafuss, Alexandra
Guillemin, Karen
Washbourne, Philip
Eisen, Judith S.
author_sort Bruckner, Joseph J.
collection PubMed
description Host-associated microbiotas guide the trajectory of developmental programs, and altered microbiota composition is linked to neurodevelopmental conditions such as autism spectrum disorder. Recent work suggests that microbiotas modulate behavioral phenotypes associated with these disorders. We discovered that the zebrafish microbiota is required for normal social behavior and reveal a molecular pathway linking the microbiota, microglial remodeling of neural circuits, and social behavior in this experimentally tractable model vertebrate. Examining neuronal correlates of behavior, we found that the microbiota restrains neurite complexity and targeting of forebrain neurons required for normal social behavior and is necessary for localization of forebrain microglia, brain-resident phagocytes that remodel neuronal arbors. The microbiota also influences microglial molecular functions, including promoting expression of the complement signaling pathway and the synaptic remodeling factor c1q. Several distinct bacterial taxa are individually sufficient for normal microglial and neuronal phenotypes, suggesting that host neuroimmune development is sensitive to a feature common among many bacteria. Our results demonstrate that the microbiota influences zebrafish social behavior by stimulating microglial remodeling of forebrain circuits during early neurodevelopment and suggest pathways for new interventions in multiple neurodevelopmental disorders.
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spelling pubmed-96244262022-11-02 The microbiota promotes social behavior by modulating microglial remodeling of forebrain neurons Bruckner, Joseph J. Stednitz, Sarah J. Grice, Max Z. Zaidan, Dana Massaquoi, Michelle S. Larsch, Johannes Tallafuss, Alexandra Guillemin, Karen Washbourne, Philip Eisen, Judith S. PLoS Biol Research Article Host-associated microbiotas guide the trajectory of developmental programs, and altered microbiota composition is linked to neurodevelopmental conditions such as autism spectrum disorder. Recent work suggests that microbiotas modulate behavioral phenotypes associated with these disorders. We discovered that the zebrafish microbiota is required for normal social behavior and reveal a molecular pathway linking the microbiota, microglial remodeling of neural circuits, and social behavior in this experimentally tractable model vertebrate. Examining neuronal correlates of behavior, we found that the microbiota restrains neurite complexity and targeting of forebrain neurons required for normal social behavior and is necessary for localization of forebrain microglia, brain-resident phagocytes that remodel neuronal arbors. The microbiota also influences microglial molecular functions, including promoting expression of the complement signaling pathway and the synaptic remodeling factor c1q. Several distinct bacterial taxa are individually sufficient for normal microglial and neuronal phenotypes, suggesting that host neuroimmune development is sensitive to a feature common among many bacteria. Our results demonstrate that the microbiota influences zebrafish social behavior by stimulating microglial remodeling of forebrain circuits during early neurodevelopment and suggest pathways for new interventions in multiple neurodevelopmental disorders. Public Library of Science 2022-11-01 /pmc/articles/PMC9624426/ /pubmed/36318534 http://dx.doi.org/10.1371/journal.pbio.3001838 Text en © 2022 Bruckner et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Bruckner, Joseph J.
Stednitz, Sarah J.
Grice, Max Z.
Zaidan, Dana
Massaquoi, Michelle S.
Larsch, Johannes
Tallafuss, Alexandra
Guillemin, Karen
Washbourne, Philip
Eisen, Judith S.
The microbiota promotes social behavior by modulating microglial remodeling of forebrain neurons
title The microbiota promotes social behavior by modulating microglial remodeling of forebrain neurons
title_full The microbiota promotes social behavior by modulating microglial remodeling of forebrain neurons
title_fullStr The microbiota promotes social behavior by modulating microglial remodeling of forebrain neurons
title_full_unstemmed The microbiota promotes social behavior by modulating microglial remodeling of forebrain neurons
title_short The microbiota promotes social behavior by modulating microglial remodeling of forebrain neurons
title_sort microbiota promotes social behavior by modulating microglial remodeling of forebrain neurons
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9624426/
https://www.ncbi.nlm.nih.gov/pubmed/36318534
http://dx.doi.org/10.1371/journal.pbio.3001838
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