Cargando…

Vasopressin deletion is associated with sex-specific shifts in the gut microbiome

Brattleboro rats harbor a spontaneous deletion of the arginine-vasopressin (Avp) gene. In addition to diabetes insipidus, these rats exhibit low levels of anxiety and depressive behaviors. Recent work on the gut-brain axis has revealed that gut microbiota can influence anxiety behaviors. Therefore,...

Descripción completa

Detalles Bibliográficos
Autores principales: Fields, Christopher T., Chassaing, Benoit, Paul, Matthew J., Gewirtz, Andrew T., de Vries, Geert J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5914910/
https://www.ncbi.nlm.nih.gov/pubmed/28759308
http://dx.doi.org/10.1080/19490976.2017.1356557
_version_ 1783316781620789248
author Fields, Christopher T.
Chassaing, Benoit
Paul, Matthew J.
Gewirtz, Andrew T.
de Vries, Geert J.
author_facet Fields, Christopher T.
Chassaing, Benoit
Paul, Matthew J.
Gewirtz, Andrew T.
de Vries, Geert J.
author_sort Fields, Christopher T.
collection PubMed
description Brattleboro rats harbor a spontaneous deletion of the arginine-vasopressin (Avp) gene. In addition to diabetes insipidus, these rats exhibit low levels of anxiety and depressive behaviors. Recent work on the gut-brain axis has revealed that gut microbiota can influence anxiety behaviors. Therefore, we studied the effects of Avp gene deletion on gut microbiota. Since Avp gene expression is sexually different, we also examined how Avp deletion affects sex differences in gut microbiota. Males and females show modest but differentiated shifts in taxa abundance across 3 separate Avp deletion genotypes: wildtype (WT), heterozygous (Het) and AVP-deficient Brattleboro (KO) rats. For each sex, we found examples of taxa that have been shown to modulate anxiety behavior, in a manner that correlates with anxiety behavior observed in homozygous knockout Brattleboro rats. One prominent example is Lactobacillus, which has been reported to be anxiolytic: Lactobacillus was found to increase in abundance in inverse proportion to increasing gene dosage (most abundant in KO rats). This genotype effect of Lactobacillus abundance was not found when females were analyzed independently. Therefore, Avp deletion appears to affect microbiota composition in a sexually differentiated manner.
format Online
Article
Text
id pubmed-5914910
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-59149102018-04-27 Vasopressin deletion is associated with sex-specific shifts in the gut microbiome Fields, Christopher T. Chassaing, Benoit Paul, Matthew J. Gewirtz, Andrew T. de Vries, Geert J. Gut Microbes Research Paper/Report Brattleboro rats harbor a spontaneous deletion of the arginine-vasopressin (Avp) gene. In addition to diabetes insipidus, these rats exhibit low levels of anxiety and depressive behaviors. Recent work on the gut-brain axis has revealed that gut microbiota can influence anxiety behaviors. Therefore, we studied the effects of Avp gene deletion on gut microbiota. Since Avp gene expression is sexually different, we also examined how Avp deletion affects sex differences in gut microbiota. Males and females show modest but differentiated shifts in taxa abundance across 3 separate Avp deletion genotypes: wildtype (WT), heterozygous (Het) and AVP-deficient Brattleboro (KO) rats. For each sex, we found examples of taxa that have been shown to modulate anxiety behavior, in a manner that correlates with anxiety behavior observed in homozygous knockout Brattleboro rats. One prominent example is Lactobacillus, which has been reported to be anxiolytic: Lactobacillus was found to increase in abundance in inverse proportion to increasing gene dosage (most abundant in KO rats). This genotype effect of Lactobacillus abundance was not found when females were analyzed independently. Therefore, Avp deletion appears to affect microbiota composition in a sexually differentiated manner. Taylor & Francis 2017-08-11 /pmc/articles/PMC5914910/ /pubmed/28759308 http://dx.doi.org/10.1080/19490976.2017.1356557 Text en © 2018 The Author(s). Published with license by Taylor & Francis http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Research Paper/Report
Fields, Christopher T.
Chassaing, Benoit
Paul, Matthew J.
Gewirtz, Andrew T.
de Vries, Geert J.
Vasopressin deletion is associated with sex-specific shifts in the gut microbiome
title Vasopressin deletion is associated with sex-specific shifts in the gut microbiome
title_full Vasopressin deletion is associated with sex-specific shifts in the gut microbiome
title_fullStr Vasopressin deletion is associated with sex-specific shifts in the gut microbiome
title_full_unstemmed Vasopressin deletion is associated with sex-specific shifts in the gut microbiome
title_short Vasopressin deletion is associated with sex-specific shifts in the gut microbiome
title_sort vasopressin deletion is associated with sex-specific shifts in the gut microbiome
topic Research Paper/Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5914910/
https://www.ncbi.nlm.nih.gov/pubmed/28759308
http://dx.doi.org/10.1080/19490976.2017.1356557
work_keys_str_mv AT fieldschristophert vasopressindeletionisassociatedwithsexspecificshiftsinthegutmicrobiome
AT chassaingbenoit vasopressindeletionisassociatedwithsexspecificshiftsinthegutmicrobiome
AT paulmatthewj vasopressindeletionisassociatedwithsexspecificshiftsinthegutmicrobiome
AT gewirtzandrewt vasopressindeletionisassociatedwithsexspecificshiftsinthegutmicrobiome
AT devriesgeertj vasopressindeletionisassociatedwithsexspecificshiftsinthegutmicrobiome