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Metabolome and microbiome profiling of a stress-sensitive rat model of gut-brain axis dysfunction
Stress negatively impacts gut and brain health. Individual differences in response to stress have been linked to genetic and environmental factors and more recently, a role for the gut microbiota in the regulation of stress-related changes has been demonstrated. However, the mechanisms by which thes...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6773725/ https://www.ncbi.nlm.nih.gov/pubmed/31575902 http://dx.doi.org/10.1038/s41598-019-50593-3 |
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author | Bassett, Shalome A. Young, Wayne Fraser, Karl Dalziel, Julie E. Webster, Jim Ryan, Leigh Fitzgerald, Patrick Stanton, Catherine Dinan, Timothy G. Cryan, John F. Clarke, Gerard Hyland, Niall Roy, Nicole C. |
author_facet | Bassett, Shalome A. Young, Wayne Fraser, Karl Dalziel, Julie E. Webster, Jim Ryan, Leigh Fitzgerald, Patrick Stanton, Catherine Dinan, Timothy G. Cryan, John F. Clarke, Gerard Hyland, Niall Roy, Nicole C. |
author_sort | Bassett, Shalome A. |
collection | PubMed |
description | Stress negatively impacts gut and brain health. Individual differences in response to stress have been linked to genetic and environmental factors and more recently, a role for the gut microbiota in the regulation of stress-related changes has been demonstrated. However, the mechanisms by which these factors influence each other are poorly understood, and there are currently no established robust biomarkers of stress susceptibility. To determine the metabolic and microbial signatures underpinning physiological stress responses, we compared stress-sensitive Wistar Kyoto (WKY) rats to the normo-anxious Sprague Dawley (SD) strain. Here we report that acute stress-induced strain-specific changes in brain lipid metabolites were a prominent feature in WKY rats. The relative abundance of Lactococcus correlated with the relative proportions of many brain lipids. In contrast, plasma lipids were significantly elevated in response to stress in SD rats, but not in WKY rats. Supporting these findings, we found that the greatest difference between the SD and WKY microbiomes were the predicted relative abundance of microbial genes involved in lipid and energy metabolism. Our results provide potential insights for developing novel biomarkers of stress vulnerability, some of which appear genotype specific. |
format | Online Article Text |
id | pubmed-6773725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67737252019-10-04 Metabolome and microbiome profiling of a stress-sensitive rat model of gut-brain axis dysfunction Bassett, Shalome A. Young, Wayne Fraser, Karl Dalziel, Julie E. Webster, Jim Ryan, Leigh Fitzgerald, Patrick Stanton, Catherine Dinan, Timothy G. Cryan, John F. Clarke, Gerard Hyland, Niall Roy, Nicole C. Sci Rep Article Stress negatively impacts gut and brain health. Individual differences in response to stress have been linked to genetic and environmental factors and more recently, a role for the gut microbiota in the regulation of stress-related changes has been demonstrated. However, the mechanisms by which these factors influence each other are poorly understood, and there are currently no established robust biomarkers of stress susceptibility. To determine the metabolic and microbial signatures underpinning physiological stress responses, we compared stress-sensitive Wistar Kyoto (WKY) rats to the normo-anxious Sprague Dawley (SD) strain. Here we report that acute stress-induced strain-specific changes in brain lipid metabolites were a prominent feature in WKY rats. The relative abundance of Lactococcus correlated with the relative proportions of many brain lipids. In contrast, plasma lipids were significantly elevated in response to stress in SD rats, but not in WKY rats. Supporting these findings, we found that the greatest difference between the SD and WKY microbiomes were the predicted relative abundance of microbial genes involved in lipid and energy metabolism. Our results provide potential insights for developing novel biomarkers of stress vulnerability, some of which appear genotype specific. Nature Publishing Group UK 2019-10-01 /pmc/articles/PMC6773725/ /pubmed/31575902 http://dx.doi.org/10.1038/s41598-019-50593-3 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Bassett, Shalome A. Young, Wayne Fraser, Karl Dalziel, Julie E. Webster, Jim Ryan, Leigh Fitzgerald, Patrick Stanton, Catherine Dinan, Timothy G. Cryan, John F. Clarke, Gerard Hyland, Niall Roy, Nicole C. Metabolome and microbiome profiling of a stress-sensitive rat model of gut-brain axis dysfunction |
title | Metabolome and microbiome profiling of a stress-sensitive rat model of gut-brain axis dysfunction |
title_full | Metabolome and microbiome profiling of a stress-sensitive rat model of gut-brain axis dysfunction |
title_fullStr | Metabolome and microbiome profiling of a stress-sensitive rat model of gut-brain axis dysfunction |
title_full_unstemmed | Metabolome and microbiome profiling of a stress-sensitive rat model of gut-brain axis dysfunction |
title_short | Metabolome and microbiome profiling of a stress-sensitive rat model of gut-brain axis dysfunction |
title_sort | metabolome and microbiome profiling of a stress-sensitive rat model of gut-brain axis dysfunction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6773725/ https://www.ncbi.nlm.nih.gov/pubmed/31575902 http://dx.doi.org/10.1038/s41598-019-50593-3 |
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