Cargando…

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

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 com...

Descripción completa

Detalles Bibliográficos
Autores principales: Doelman, Adam, Tigchelaar, Seth, McConeghy, Brian, Sinha, Sunita, Keung, Martin S., Manouchehri, Neda, Webster, Megan, Fisk, Shera, Morrison, Charlotte, Streijger, Femke, Nislow, Corey, Kwon, Brian K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8557039/
https://www.ncbi.nlm.nih.gov/pubmed/34717545
http://dx.doi.org/10.1186/s12864-021-07979-3
_version_ 1784592294763036672
author Doelman, Adam
Tigchelaar, Seth
McConeghy, Brian
Sinha, Sunita
Keung, Martin S.
Manouchehri, Neda
Webster, Megan
Fisk, Shera
Morrison, Charlotte
Streijger, Femke
Nislow, Corey
Kwon, Brian K.
author_facet Doelman, Adam
Tigchelaar, Seth
McConeghy, Brian
Sinha, Sunita
Keung, Martin S.
Manouchehri, Neda
Webster, Megan
Fisk, Shera
Morrison, Charlotte
Streijger, Femke
Nislow, Corey
Kwon, Brian K.
author_sort Doelman, Adam
collection PubMed
description 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: 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: 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07979-3.
format Online
Article
Text
id pubmed-8557039
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-85570392021-11-01 Characterization of the gut microbiome in a porcine model of thoracic spinal cord injury Doelman, Adam Tigchelaar, Seth McConeghy, Brian Sinha, Sunita Keung, Martin S. Manouchehri, Neda Webster, Megan Fisk, Shera Morrison, Charlotte Streijger, Femke Nislow, Corey Kwon, Brian K. BMC Genomics Research 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: 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: 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07979-3. BioMed Central 2021-10-30 /pmc/articles/PMC8557039/ /pubmed/34717545 http://dx.doi.org/10.1186/s12864-021-07979-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Doelman, Adam
Tigchelaar, Seth
McConeghy, Brian
Sinha, Sunita
Keung, Martin S.
Manouchehri, Neda
Webster, Megan
Fisk, Shera
Morrison, Charlotte
Streijger, Femke
Nislow, Corey
Kwon, Brian K.
Characterization of the gut microbiome in a porcine model of thoracic spinal cord injury
title Characterization of the gut microbiome in a porcine model of thoracic spinal cord injury
title_full Characterization of the gut microbiome in a porcine model of thoracic spinal cord injury
title_fullStr Characterization of the gut microbiome in a porcine model of thoracic spinal cord injury
title_full_unstemmed Characterization of the gut microbiome in a porcine model of thoracic spinal cord injury
title_short Characterization of the gut microbiome in a porcine model of thoracic spinal cord injury
title_sort characterization of the gut microbiome in a porcine model of thoracic spinal cord injury
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8557039/
https://www.ncbi.nlm.nih.gov/pubmed/34717545
http://dx.doi.org/10.1186/s12864-021-07979-3
work_keys_str_mv AT doelmanadam characterizationofthegutmicrobiomeinaporcinemodelofthoracicspinalcordinjury
AT tigchelaarseth characterizationofthegutmicrobiomeinaporcinemodelofthoracicspinalcordinjury
AT mcconeghybrian characterizationofthegutmicrobiomeinaporcinemodelofthoracicspinalcordinjury
AT sinhasunita characterizationofthegutmicrobiomeinaporcinemodelofthoracicspinalcordinjury
AT keungmartins characterizationofthegutmicrobiomeinaporcinemodelofthoracicspinalcordinjury
AT manouchehrineda characterizationofthegutmicrobiomeinaporcinemodelofthoracicspinalcordinjury
AT webstermegan characterizationofthegutmicrobiomeinaporcinemodelofthoracicspinalcordinjury
AT fiskshera characterizationofthegutmicrobiomeinaporcinemodelofthoracicspinalcordinjury
AT morrisoncharlotte characterizationofthegutmicrobiomeinaporcinemodelofthoracicspinalcordinjury
AT streijgerfemke characterizationofthegutmicrobiomeinaporcinemodelofthoracicspinalcordinjury
AT nislowcorey characterizationofthegutmicrobiomeinaporcinemodelofthoracicspinalcordinjury
AT kwonbriank characterizationofthegutmicrobiomeinaporcinemodelofthoracicspinalcordinjury