Altered fecal microbiota composition in all male aggressor‐exposed rodent model simulating features of post‐traumatic stress disorder

The bidirectional role of gut–brain axis that integrates the gut and central nervous system activities has recently been investigated. We studied “cage‐within‐cage resident‐intruder” all‐male model, where subject male mice (C57BL/6J) are exposed to aggressor mice (SJL albino), and gut microbiota‐der...

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Published inJournal of neuroscience research Vol. 96; no. 7; pp. 1311 - 1323
Main Authors Gautam, Aarti, Kumar, Raina, Chakraborty, Nabarun, Muhie, Seid, Hoke, Allison, Hammamieh, Rasha, Jett, Marti
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.07.2018
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Abstract The bidirectional role of gut–brain axis that integrates the gut and central nervous system activities has recently been investigated. We studied “cage‐within‐cage resident‐intruder” all‐male model, where subject male mice (C57BL/6J) are exposed to aggressor mice (SJL albino), and gut microbiota‐derived metabolites were identified in plasma after 10 days of exposure. We assessed 16S ribosomal RNA gene from fecal samples collected daily from these mice during the 10‐day study. Alpha diversity using Chao indices indicated no change in diversity in aggressor‐exposed samples. The abundance profile showed the top phyla were Firmicutes and Bacteroidetes, Tenericutes, Verrucomicrobia, Actinobacteria and Proteobacteria, respectively. The phyla Firmicutes and Bacteroidetes are vulnerable to PTSD‐eliciting stress and the Firmicutes/Bacteroidetes ratio increases with stress. Principal coordinate analysis showed the control and aggressor‐exposed samples cluster separately where samples from early time points (day 1‐3) clustered together and were distinct from late time points (day 4‐9). The genus‐based analysis revealed all control time points clustered together and aggressor‐exposed samples had multiple clusters. The decrease in proportion of Firmicutes after aggressor exposure persisted throughout the study. The proportion of Verrucomicrobia immediately decreased and was significantly shifted at most of the later time points. The genus Oscillospira, Lactobacillus, Akkermansia and Anaeroplasma are the top four genera that differed between control and stressor‐exposed mice. The data showed immediate effect on microbiome composition during a 10 day time period of stress exposure. Studying the longitudinal effects of a stressor is an important step toward an improved mechanistic understanding of the microbiome dynamics.
AbstractList The bidirectional role of gut-brain axis that integrates the gut and central nervous system activities has recently been investigated. We studied "cage-within-cage resident-intruder" all-male model, where subject male mice (C57BL/6J) are exposed to aggressor mice (SJL albino), and gut microbiota-derived metabolites were identified in plasma after 10 days of exposure. We assessed 16S ribosomal RNA gene from fecal samples collected daily from these mice during the 10-day study. Alpha diversity using Chao indices indicated no change in diversity in aggressor-exposed samples. The abundance profile showed the top phyla were Firmicutes and Bacteroidetes, Tenericutes, Verrucomicrobia, Actinobacteria and Proteobacteria, respectively. The phyla Firmicutes and Bacteroidetes are vulnerable to PTSD-eliciting stress and the Firmicutes/Bacteroidetes ratio increases with stress. Principal coordinate analysis showed the control and aggressor-exposed samples cluster separately where samples from early time points (day 1-3) clustered together and were distinct from late time points (day 4-9). The genus-based analysis revealed all control time points clustered together and aggressor-exposed samples had multiple clusters. The decrease in proportion of Firmicutes after aggressor exposure persisted throughout the study. The proportion of Verrucomicrobia immediately decreased and was significantly shifted at most of the later time points. The genus Oscillospira, Lactobacillus, Akkermansia and Anaeroplasma are the top four genera that differed between control and stressor-exposed mice. The data showed immediate effect on microbiome composition during a 10 day time period of stress exposure. Studying the longitudinal effects of a stressor is an important step toward an improved mechanistic understanding of the microbiome dynamics.The bidirectional role of gut-brain axis that integrates the gut and central nervous system activities has recently been investigated. We studied "cage-within-cage resident-intruder" all-male model, where subject male mice (C57BL/6J) are exposed to aggressor mice (SJL albino), and gut microbiota-derived metabolites were identified in plasma after 10 days of exposure. We assessed 16S ribosomal RNA gene from fecal samples collected daily from these mice during the 10-day study. Alpha diversity using Chao indices indicated no change in diversity in aggressor-exposed samples. The abundance profile showed the top phyla were Firmicutes and Bacteroidetes, Tenericutes, Verrucomicrobia, Actinobacteria and Proteobacteria, respectively. The phyla Firmicutes and Bacteroidetes are vulnerable to PTSD-eliciting stress and the Firmicutes/Bacteroidetes ratio increases with stress. Principal coordinate analysis showed the control and aggressor-exposed samples cluster separately where samples from early time points (day 1-3) clustered together and were distinct from late time points (day 4-9). The genus-based analysis revealed all control time points clustered together and aggressor-exposed samples had multiple clusters. The decrease in proportion of Firmicutes after aggressor exposure persisted throughout the study. The proportion of Verrucomicrobia immediately decreased and was significantly shifted at most of the later time points. The genus Oscillospira, Lactobacillus, Akkermansia and Anaeroplasma are the top four genera that differed between control and stressor-exposed mice. The data showed immediate effect on microbiome composition during a 10 day time period of stress exposure. Studying the longitudinal effects of a stressor is an important step toward an improved mechanistic understanding of the microbiome dynamics.
The bidirectional role of gut–brain axis that integrates the gut and central nervous system activities has recently been investigated. We studied “cage‐within‐cage resident‐intruder” all‐male model, where subject male mice (C57BL/6J) are exposed to aggressor mice (SJL albino), and gut microbiota‐derived metabolites were identified in plasma after 10 days of exposure. We assessed 16S ribosomal RNA gene from fecal samples collected daily from these mice during the 10‐day study. Alpha diversity using Chao indices indicated no change in diversity in aggressor‐exposed samples. The abundance profile showed the top phyla were Firmicutes and Bacteroidetes , Tenericutes , Verrucomicrobia , Actinobacteria and Proteobacteria , respectively. The phyla Firmicutes and Bacteroidetes are vulnerable to PTSD‐eliciting stress and the Firmicutes/Bacteroidetes ratio increases with stress. Principal coordinate analysis showed the control and aggressor‐exposed samples cluster separately where samples from early time points (day 1‐3) clustered together and were distinct from late time points (day 4‐9). The genus‐based analysis revealed all control time points clustered together and aggressor‐exposed samples had multiple clusters. The decrease in proportion of Firmicutes after aggressor exposure persisted throughout the study. The proportion of Verrucomicrobia immediately decreased and was significantly shifted at most of the later time points. The genus Oscillospira , Lactobacillus , Akkermansia and Anaeroplasma are the top four genera that differed between control and stressor‐exposed mice. The data showed immediate effect on microbiome composition during a 10 day time period of stress exposure. Studying the longitudinal effects of a stressor is an important step toward an improved mechanistic understanding of the microbiome dynamics.
The bidirectional role of gut-brain axis that integrates the gut and central nervous system activities has recently been investigated. We studied "cage-within-cage resident-intruder" all-male model, where subject male mice (C57BL/6J) are exposed to aggressor mice (SJL albino), and gut microbiota-derived metabolites were identified in plasma after 10 days of exposure. We assessed 16S ribosomal RNA gene from fecal samples collected daily from these mice during the 10-day study. Alpha diversity using Chao indices indicated no change in diversity in aggressor-exposed samples. The abundance profile showed the top phyla were Firmicutes and Bacteroidetes, Tenericutes, Verrucomicrobia, Actinobacteria and Proteobacteria, respectively. The phyla Firmicutes and Bacteroidetes are vulnerable to PTSD-eliciting stress and the Firmicutes/Bacteroidetes ratio increases with stress. Principal coordinate analysis showed the control and aggressor-exposed samples cluster separately where samples from early time points (day 1-3) clustered together and were distinct from late time points (day 4-9). The genus-based analysis revealed all control time points clustered together and aggressor-exposed samples had multiple clusters. The decrease in proportion of Firmicutes after aggressor exposure persisted throughout the study. The proportion of Verrucomicrobia immediately decreased and was significantly shifted at most of the later time points. The genus Oscillospira, Lactobacillus, Akkermansia and Anaeroplasma are the top four genera that differed between control and stressor-exposed mice. The data showed immediate effect on microbiome composition during a 10 day time period of stress exposure. Studying the longitudinal effects of a stressor is an important step toward an improved mechanistic understanding of the microbiome dynamics.
Author Hoke, Allison
Hammamieh, Rasha
Chakraborty, Nabarun
Muhie, Seid
Jett, Marti
Kumar, Raina
Gautam, Aarti
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IsPeerReviewed true
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Issue 7
Keywords Bacteriodetes
PTSD
16S rRNA
stress
metagenomics
resident-intruder
C57BL/6J
microbiome
social defeat
Firmicutes
Language English
License 2018 Wiley Periodicals, Inc.
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Notes Funding information
Our current study is the extension of previously published studies of the rodent model simulating features of PTSD. The paper provides the time series analysis of microbiome composition during the psychological stress as observed by 16S amplicon sequencing in mouse fecal samples.
The support from USAMRMC, grant number 09284002 is gratefully acknowledged
Firmicutes/Bacteriodetes
ratio increased after stress. The psychological disturbances led to instability of the microbiota early during the exposures. The effects of a stressor in a longitudinal study are an important step toward an improved mechanistic understanding of the microbiome dynamics.
We observed changes in microbiome composition as early as 24h post‐stressor incident in exposed animals where the
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Snippet The bidirectional role of gut–brain axis that integrates the gut and central nervous system activities has recently been investigated. We studied...
The bidirectional role of gut-brain axis that integrates the gut and central nervous system activities has recently been investigated. We studied...
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SubjectTerms 16S rRNA
Animals
Bacteriodetes
Bacteroidetes
Bacteroidetes - isolation & purification
Brain
C57BL/6J
Cages
Central nervous system
Composition effects
Computer simulation
Exposure
Fecal microflora
Feces - microbiology
Firmicutes
Firmicutes - isolation & purification
Gastrointestinal Microbiome
Intestinal microflora
Male
Metabolites
metagenomics
Mice
Mice, Inbred C57BL
microbiome
Microbiomes
Microbiota
Models, Animal
Post traumatic stress disorder
Proteobacteria - isolation & purification
PTSD
resident‐intruder
Ribonucleic acid
RNA
rRNA 16S
social defeat
stress
Stress Disorders, Post-Traumatic - microbiology
Stresses
Verrucomicrobia
Title Altered fecal microbiota composition in all male aggressor‐exposed rodent model simulating features of post‐traumatic stress disorder
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjnr.24229
https://www.ncbi.nlm.nih.gov/pubmed/29633335
https://www.proquest.com/docview/2047324598
https://www.proquest.com/docview/2023729950
Volume 96
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