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Gut dysbiosis impairs recovery after spinal cord injury

The trillions of microbes that exist in the gastrointestinal tract have emerged as pivotal regulators of mammalian development and physiology. Disruption of this gut microbiome, a process known as dysbiosis, causes or exacerbates various diseases, but whether gut dysbiosis affects recovery of neurol...

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Autores principales: Kigerl, Kristina A., Hall, Jodie C.E., Wang, Lingling, Mo, Xiaokui, Yu, Zhongtang, Popovich, Phillip G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5110012/
https://www.ncbi.nlm.nih.gov/pubmed/27810921
http://dx.doi.org/10.1084/jem.20151345
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author Kigerl, Kristina A.
Hall, Jodie C.E.
Wang, Lingling
Mo, Xiaokui
Yu, Zhongtang
Popovich, Phillip G.
author_facet Kigerl, Kristina A.
Hall, Jodie C.E.
Wang, Lingling
Mo, Xiaokui
Yu, Zhongtang
Popovich, Phillip G.
author_sort Kigerl, Kristina A.
collection PubMed
description The trillions of microbes that exist in the gastrointestinal tract have emerged as pivotal regulators of mammalian development and physiology. Disruption of this gut microbiome, a process known as dysbiosis, causes or exacerbates various diseases, but whether gut dysbiosis affects recovery of neurological function or lesion pathology after traumatic spinal cord injury (SCI) is unknown. Data in this study show that SCI increases intestinal permeability and bacterial translocation from the gut. These changes are associated with immune cell activation in gut-associated lymphoid tissues (GALTs) and significant changes in the composition of both major and minor gut bacterial taxa. Postinjury changes in gut microbiota persist for at least one month and predict the magnitude of locomotor impairment. Experimental induction of gut dysbiosis in naive mice before SCI (e.g., via oral delivery of broad-spectrum antibiotics) exacerbates neurological impairment and spinal cord pathology after SCI. Conversely, feeding SCI mice commercial probiotics (VSL#3) enriched with lactic acid–producing bacteria triggers a protective immune response in GALTs and confers neuroprotection with improved locomotor recovery. Our data reveal a previously unknown role for the gut microbiota in influencing recovery of neurological function and neuropathology after SCI.
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spelling pubmed-51100122017-05-14 Gut dysbiosis impairs recovery after spinal cord injury Kigerl, Kristina A. Hall, Jodie C.E. Wang, Lingling Mo, Xiaokui Yu, Zhongtang Popovich, Phillip G. J Exp Med Research Articles The trillions of microbes that exist in the gastrointestinal tract have emerged as pivotal regulators of mammalian development and physiology. Disruption of this gut microbiome, a process known as dysbiosis, causes or exacerbates various diseases, but whether gut dysbiosis affects recovery of neurological function or lesion pathology after traumatic spinal cord injury (SCI) is unknown. Data in this study show that SCI increases intestinal permeability and bacterial translocation from the gut. These changes are associated with immune cell activation in gut-associated lymphoid tissues (GALTs) and significant changes in the composition of both major and minor gut bacterial taxa. Postinjury changes in gut microbiota persist for at least one month and predict the magnitude of locomotor impairment. Experimental induction of gut dysbiosis in naive mice before SCI (e.g., via oral delivery of broad-spectrum antibiotics) exacerbates neurological impairment and spinal cord pathology after SCI. Conversely, feeding SCI mice commercial probiotics (VSL#3) enriched with lactic acid–producing bacteria triggers a protective immune response in GALTs and confers neuroprotection with improved locomotor recovery. Our data reveal a previously unknown role for the gut microbiota in influencing recovery of neurological function and neuropathology after SCI. The Rockefeller University Press 2016-11-14 /pmc/articles/PMC5110012/ /pubmed/27810921 http://dx.doi.org/10.1084/jem.20151345 Text en © 2016 Kigerl et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Kigerl, Kristina A.
Hall, Jodie C.E.
Wang, Lingling
Mo, Xiaokui
Yu, Zhongtang
Popovich, Phillip G.
Gut dysbiosis impairs recovery after spinal cord injury
title Gut dysbiosis impairs recovery after spinal cord injury
title_full Gut dysbiosis impairs recovery after spinal cord injury
title_fullStr Gut dysbiosis impairs recovery after spinal cord injury
title_full_unstemmed Gut dysbiosis impairs recovery after spinal cord injury
title_short Gut dysbiosis impairs recovery after spinal cord injury
title_sort gut dysbiosis impairs recovery after spinal cord injury
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5110012/
https://www.ncbi.nlm.nih.gov/pubmed/27810921
http://dx.doi.org/10.1084/jem.20151345
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