Literature DB >> 34403735

Parabacteroides distasonis induces depressive-like behavior in a mouse model of Crohn's disease.

Adrian Gomez-Nguyen1, Abigail R Basson1, Luc Dark-Fleury1, Kristen Hsu1, Abdullah Osme2, Paola Menghini1, Theresa T Pizarro3, Fabio Cominelli4.   

Abstract

Patients with inflammatory bowel disease (IBD) are particularly susceptible to behavioral diagnoses, and the microbiome has been repeatedly implicated in the pathogenesis of IBD. The intestinal microbiome's ability to affect behavior has become increasingly recognized and studied. The so-called 'psychobiome' has been linked to a plethora of neurological and psychological diagnoses, including autism and Parkinson's disease. Despite the ability of many bacterial species within the human intestinal microbiome to synthesize neurotransmitters, it has never been previously reported that a single bacterial species is sufficient to induce depression. Here, we demonstrate that our mouse model of Crohn's disease (CD)-like ileitis, the SAMP1/YitFc (SAMP1), does not exhibit baseline behavioral abnormalities. By comparison, SAMP6 mice develop depressive-like behavior that is associated with a rise in the GABA-producing bacterial genus Parabacteroides. We finally demonstrate that administration of Parabacteroides distasonis into our SAMP1 mice induces depressive-like behavior. Colonization with P. distasonis was not associated with increased intestinal inflammation or alterations in other measures of behavior. The intestinal environment of CD may be particularly conducive to colonization with P. distasonis and subsequent induction of depressive-like behavior. To our knowledge, this is the first report of a bacterial species specifically inducing depressive-like behavior.
Copyright © 2021 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Crohn’s disease; Inflammatory bowel disease; Major depressive disorder; Microbiome; Microbiome-gut-brain axis; Parabacteroides distasonis; Psychobiome

Mesh:

Year:  2021        PMID: 34403735      PMCID: PMC9217177          DOI: 10.1016/j.bbi.2021.08.218

Source DB:  PubMed          Journal:  Brain Behav Immun        ISSN: 0889-1591            Impact factor:   19.227


  32 in total

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