Cited by 236Probiotics and Fermented FoodsGut microbiota and healthStress Responses and Cortisol

Oral treatment with Lactobacillus rhamnosus attenuates behavioural deficits and immune changes in chronic social stress

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Bharwani, Aadil, Mian, M. Firoz, Surette, Michael G., Bienenstock, John, Forsythe, Paul·2017·BMC Medicine

Abstract

BACKGROUND: Stress-related disorders involve systemic alterations, including disruption of the intestinal microbial community. Given the putative connections between the microbiota, immunity, neural function, and behaviour, we investigated the potential for microbe-induced gut-to-brain signalling to modulate the impact of stress on host behaviour and immunoregulation. METHODS: Male C57BL/6 mice treated orally over 28 days with either Lactobacillus rhamnosus (JB-1) ™ or vehicle were subjected to chronic social defeat and assessed for alterations in behaviour and immune cell phenotype. 16S rRNA sequencing and mass spectrometry were employed to analyse the faecal microbial community and metabolite profile. RESULTS: Treatment with JB-1 decreased stress-induced anxiety-like behaviour and prevented deficits in social interaction with conspecifics. However, JB-1 did not alter development of aggressor avoidance following social defeat. Microbial treatment attenuated stress-related activation of dendritic cells while increasing IL-10+ regulatory T cells. Furthermore, JB-1 modulated the effect of stress on faecal metabolites with neuroactive and immunomodulatory properties. Exposure to social defeat altered faecal microbial community composition and reduced species richness and diversity, none of which was prevented by JB-1. Stress-related microbiota disruptions persisted in vehicle-treated mice for 3 weeks following stressor cessation. CONCLUSIONS: These data demonstrate that despite the complexity of the gut microbiota, exposure to a single microbial strain can protect against certain stress-induced behaviours and systemic immune alterations without preventing dysbiosis. This work supports microbe-based interventions for stress-related disorders.

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Authors
Bharwani, A., Mian, M. F., Surette, M. G., Bienenstock, J., & Forsythe, P.
Affiliations
  • McMaster University (CA)
  • St. Joseph’s Healthcare Hamilton (CA)
Corresponding author
Forsythe, Paul
Venue
BMC Medicine
Published
2017-01-11
Volume
15
Issue
1
Pages
7-7
ISSN
1741-7015 (ISSN-L)
OpenAlex
W2571218087
Cited by
236
References
19
Citations by year
2026: 11 · 2025: 22 · 2024: 24 · 2023: 24 · 2022: 30 · 2021: 26 · 2020: 27 · 2019: 30 · 2018: 30 · 2017: 12
FWCI
30.47
Type
journal article
Language
en
Open access
Locations
  • BMC Medicine (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
Funders
  • Office of Naval Research (N00014-14-1-0787)
  • Canada Research Chairs
Topics
  • Life Sciences › Agricultural and Biological Sciences › Food Science › Probiotics and Fermented Foods
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
  • Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
Keywords
chronic social defeat, chronic social stress, gut microbiota, anxiety-like behavior, social interaction deficits, dendritic cells, regulatory T cells, IL-10, fecal metabolites, neuroactive metabolites, stress-related disorders, dysbiosis, gut-brain axis, immunomodulation
MeSH terms
Gastrointestinal Microbiome, Animals, Anxiety, Behavior, Animal, Brain, Male, Mice, Inbred C57BL, RNA, Ribosomal, 16S, Stress, Psychological, Interleukin-10, Probiotics, Mice, Lacticaseibacillus rhamnosus

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