Abstract

The association between the shift in fecal resident microbiome and social conflicts with long-term consequences on psychological plasticity, such as the development of post-traumatic stress disorder (PTSD), is yet to be comprehended. We developed an aggressor-exposed (Agg-E) social stress (SS) mouse model to mimic warzone-like conflicts, where random life-threatening interactions took place between naïve intruder mice and aggressive resident mice. Gradually these Agg-E mice developed distinct characteristics simulating PTSD-like aspects, whereas the control mice not exposed to Agg-E SS demonstrated distinct phenotypes. To further investigate the role of Agg-E SS on the resident microbiome, 16S rRNA gene sequencing was assayed using fecal samples collected at pre-, during, and post-SS time points. A time agonist shift in the fecal microbial composition of Agg-E mice in contrast to its controls suggested a persistent impact of Agg-E SS on resident microbiota. At the taxonomic level, Agg-E SS caused a significant shift in the time-resolved ratios of Firmicutes and Bacteroidetes abundance. Furthermore, Agg-E SS caused diverging shifts in the relative abundances of Verrucomicrobia and Actinobacteria. An in silico estimation of genomic potential identified a potentially perturbed cluster of bioenergetic networks, which became increasingly enriched with time since the termination of Agg-E SS. Supported by a growing number of studies, our results indicated the roles of the microbiome in a wide range of phenotypes that could mimic the comorbidities of PTSD, which would be directly influenced by energy deficiency. Together, the present work suggested the fecal microbiome as a potential tool to manage long-term effects of social conflicts, including the management of PTSD.

Highlights

  • There is increased interest in the gut-brain axis and the potential role of the gut microbiome in regulating the mental health of the host (Clapp et al, 2017; Dinan and Cryan, 2017; Osadchiy et al, 2019)

  • We are focusing on post-traumatic stress disorder (PTSD), which is a condition of persistent mental and emotional stress that is typically triggered by experiencing life-threatening events (Battle, 2013)

  • PTSD has persistent symptoms that include reexperiencing of the traumatic event, avoidance of stimuli associated with the trauma, numbing, significant distress, and social impairment (Battle, 2013; Auxemery, 2018)

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Summary

Introduction

There is increased interest in the gut-brain axis and the potential role of the gut microbiome in regulating the mental health of the host (Clapp et al, 2017; Dinan and Cryan, 2017; Osadchiy et al, 2019). Studies suggested a bidirectional relationship between the host and the microbiome (Clapp et al, 2017; Dinan and Cryan, 2017; Osadchiy et al, 2019), and understanding and modeling of this relationship could result in diagnostic markers of the host stress response, and a way to identify precision treatments. We are focusing on post-traumatic stress disorder (PTSD), which is a condition of persistent mental and emotional stress that is typically triggered by experiencing life-threatening events (Battle, 2013). To study the gut microbiome and its role and function in disease, murine models remain the most popular choice (Nguyen et al, 2015; Schoner et al, 2017). Limitations of the murine model include that despite principal similarities, the mouse model cannot fully capture human systems, the interaction between the gut and the host is hostspecific, using a mouse model may not be as applicable in humans, and the inbred mouse strains does not capture the genetic variations found the human populations (Nguyen et al, 2015)

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