Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Arentsen, Tim, Raith, Henrike, Qian, Yu, Forssberg, Hans, Heijtz, Rochellys Diaz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2015
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
_version_ 1782406129765056512
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
work_keys_str_mv AT arentsentim hostmicrobiotamodulatesdevelopmentofsocialpreferenceinmice
AT raithhenrike hostmicrobiotamodulatesdevelopmentofsocialpreferenceinmice
AT qianyu hostmicrobiotamodulatesdevelopmentofsocialpreferenceinmice
AT forssberghans hostmicrobiotamodulatesdevelopmentofsocialpreferenceinmice
AT heijtzrochellysdiaz hostmicrobiotamodulatesdevelopmentofsocialpreferenceinmice