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Host microbiota modulates development of social preference in mice
BACKGROUND: Mounting evidence indicates that the indigenous gut microbiota exerts long-lasting programming effects on brain function and behaviour. OBJECTIVE: In this study, we used the germ-free (GF) mouse model, devoid of any microbiota throughout development, to assess the influence of the indige...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Co-Action Publishing
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683992/ https://www.ncbi.nlm.nih.gov/pubmed/26679775 http://dx.doi.org/10.3402/mehd.v26.29719 |
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author | Arentsen, Tim Raith, Henrike Qian, Yu Forssberg, Hans Heijtz, Rochellys Diaz |
author_facet | Arentsen, Tim Raith, Henrike Qian, Yu Forssberg, Hans Heijtz, Rochellys Diaz |
author_sort | Arentsen, Tim |
collection | PubMed |
description | BACKGROUND: Mounting evidence indicates that the indigenous gut microbiota exerts long-lasting programming effects on brain function and behaviour. OBJECTIVE: In this study, we used the germ-free (GF) mouse model, devoid of any microbiota throughout development, to assess the influence of the indigenous microbiota on social preference and repetitive behaviours (e.g. self-grooming). METHODS AND RESULTS: Using the three-chambered social approach task, we demonstrate that when adult GF mice were given a choice to spend time with a novel mouse or object, they spent significantly more time sniffing and interacting with the stimulus mouse compared to conventionally raised mice (specific pathogen-free, SPF). Time spent in repetitive self-grooming behaviour, however, did not differ between GF and SPF mice. Real-time PCR–based gene expression analysis of the amygdala, a key region that is part of the social brain network, revealed a significant reduction in the mRNA levels of total brain-derived neurotrophic factor (BDNF), BDNF exon I-, IV-, VI-, IX-containing transcripts, and NGFI-A (a signalling molecule downstream of BDNF) in GF mice compared to SPF mice. CONCLUSION: These results suggest that differential regulation of BDNF exon transcripts in the amygdala by the indigenous microbes may contribute to the altered social development of GF mice. |
format | Online Article Text |
id | pubmed-4683992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Co-Action Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-46839922016-01-05 Host microbiota modulates development of social preference in mice Arentsen, Tim Raith, Henrike Qian, Yu Forssberg, Hans Heijtz, Rochellys Diaz Microb Ecol Health Dis Original Article BACKGROUND: Mounting evidence indicates that the indigenous gut microbiota exerts long-lasting programming effects on brain function and behaviour. OBJECTIVE: In this study, we used the germ-free (GF) mouse model, devoid of any microbiota throughout development, to assess the influence of the indigenous microbiota on social preference and repetitive behaviours (e.g. self-grooming). METHODS AND RESULTS: Using the three-chambered social approach task, we demonstrate that when adult GF mice were given a choice to spend time with a novel mouse or object, they spent significantly more time sniffing and interacting with the stimulus mouse compared to conventionally raised mice (specific pathogen-free, SPF). Time spent in repetitive self-grooming behaviour, however, did not differ between GF and SPF mice. Real-time PCR–based gene expression analysis of the amygdala, a key region that is part of the social brain network, revealed a significant reduction in the mRNA levels of total brain-derived neurotrophic factor (BDNF), BDNF exon I-, IV-, VI-, IX-containing transcripts, and NGFI-A (a signalling molecule downstream of BDNF) in GF mice compared to SPF mice. CONCLUSION: These results suggest that differential regulation of BDNF exon transcripts in the amygdala by the indigenous microbes may contribute to the altered social development of GF mice. Co-Action Publishing 2015-12-15 /pmc/articles/PMC4683992/ /pubmed/26679775 http://dx.doi.org/10.3402/mehd.v26.29719 Text en © 2015 TimArentsen et al. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Arentsen, Tim Raith, Henrike Qian, Yu Forssberg, Hans Heijtz, Rochellys Diaz Host microbiota modulates development of social preference in mice |
title | Host microbiota modulates development of social preference in mice |
title_full | Host microbiota modulates development of social preference in mice |
title_fullStr | Host microbiota modulates development of social preference in mice |
title_full_unstemmed | Host microbiota modulates development of social preference in mice |
title_short | Host microbiota modulates development of social preference in mice |
title_sort | host microbiota modulates development of social preference in mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683992/ https://www.ncbi.nlm.nih.gov/pubmed/26679775 http://dx.doi.org/10.3402/mehd.v26.29719 |
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