Characterization of the gut microbiome in a porcine model of thoracic spinal cord injury.


Journal

BMC genomics
ISSN: 1471-2164
Titre abrégé: BMC Genomics
Pays: England
ID NLM: 100965258

Informations de publication

Date de publication:
30 Oct 2021
Historique:
received: 21 01 2021
accepted: 01 09 2021
entrez: 31 10 2021
pubmed: 1 11 2021
medline: 3 11 2021
Statut: epublish

Résumé

The gut microbiome is a diverse network of bacteria which inhabit our digestive tract and is crucial for efficient cellular metabolism, nutrient absorption, and immune system development. Spinal cord injury (SCI) disrupts autonomic function below the level of injury and can alter the composition of the gut microbiome. Studies in rodent models have shown that SCI-induced bacterial imbalances in the gut can exacerbate the spinal cord damage and impair recovery. In this study we, for the first time, characterized the composition of the gut microbiome in a Yucatan minipig SCI model. We compared the relative abundance of the most dominant bacterial phyla in control samples to those collected from animals who underwent a contusion-compression SCI at the 2nd or 10th Thoracic level. We identify specific bacterial fluctuations that are unique to SCI animals, which were not found in uninjured animals given the same dietary regimen or antibiotic administration. Further, we identified a specific time-frame, "SCI-acute stage", during which many of these bacterial fluctuations occur before returning to "baseline" levels. This work presents a dynamic view of the microbiome changes that accompany SCI, establishes a resource for future studies and to understand the changes that occur to gut microbiota after spinal cord injury and may point to a potential therapeutic target for future treatment.

Sections du résumé

BACKGROUND BACKGROUND
The gut microbiome is a diverse network of bacteria which inhabit our digestive tract and is crucial for efficient cellular metabolism, nutrient absorption, and immune system development. Spinal cord injury (SCI) disrupts autonomic function below the level of injury and can alter the composition of the gut microbiome. Studies in rodent models have shown that SCI-induced bacterial imbalances in the gut can exacerbate the spinal cord damage and impair recovery. In this study we, for the first time, characterized the composition of the gut microbiome in a Yucatan minipig SCI model. We compared the relative abundance of the most dominant bacterial phyla in control samples to those collected from animals who underwent a contusion-compression SCI at the 2nd or 10th Thoracic level.
RESULTS RESULTS
We identify specific bacterial fluctuations that are unique to SCI animals, which were not found in uninjured animals given the same dietary regimen or antibiotic administration. Further, we identified a specific time-frame, "SCI-acute stage", during which many of these bacterial fluctuations occur before returning to "baseline" levels.
CONCLUSION CONCLUSIONS
This work presents a dynamic view of the microbiome changes that accompany SCI, establishes a resource for future studies and to understand the changes that occur to gut microbiota after spinal cord injury and may point to a potential therapeutic target for future treatment.

Identifiants

pubmed: 34717545
doi: 10.1186/s12864-021-07979-3
pii: 10.1186/s12864-021-07979-3
pmc: PMC8557039
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

775

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2021. The Author(s).

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Auteurs

Adam Doelman (A)

International Collaboration on Repair Discoveries, University of British Columbia, Vancouver, BC, Canada.

Seth Tigchelaar (S)

International Collaboration on Repair Discoveries, University of British Columbia, Vancouver, BC, Canada.

Brian McConeghy (B)

Sequencing and Bioinformatics Consortium, University of British Columbia, Vancouver, BC, Canada.

Sunita Sinha (S)

Sequencing and Bioinformatics Consortium, University of British Columbia, Vancouver, BC, Canada.

Martin S Keung (MS)

International Collaboration on Repair Discoveries, University of British Columbia, Vancouver, BC, Canada.

Neda Manouchehri (N)

International Collaboration on Repair Discoveries, University of British Columbia, Vancouver, BC, Canada.

Megan Webster (M)

International Collaboration on Repair Discoveries, University of British Columbia, Vancouver, BC, Canada.

Shera Fisk (S)

International Collaboration on Repair Discoveries, University of British Columbia, Vancouver, BC, Canada.

Charlotte Morrison (C)

International Collaboration on Repair Discoveries, University of British Columbia, Vancouver, BC, Canada.

Femke Streijger (F)

International Collaboration on Repair Discoveries, University of British Columbia, Vancouver, BC, Canada.

Corey Nislow (C)

Sequencing and Bioinformatics Consortium, University of British Columbia, Vancouver, BC, Canada.

Brian K Kwon (BK)

International Collaboration on Repair Discoveries, University of British Columbia, Vancouver, BC, Canada. brian.kwon@ubc.ca.
Department of Orthopedics, Vancouver Spine Surgery Institute, University of British Columbia, Vancouver, BC, Canada. brian.kwon@ubc.ca.

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