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Age-dependent remodeling of gut microbiome and host serum metabolome in mice
The interplay between microbiota and host metabolism plays an important role in health. Here, we examined the relationship between age, gut microbiome and host serum metabolites in male C57BL/6J mice. Fecal microbiome analysis of 3, 6, 18, and 28 months (M) old mice showed that the Firmicutes/Bacter...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Impact Journals
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7993679/ https://www.ncbi.nlm.nih.gov/pubmed/33612480 http://dx.doi.org/10.18632/aging.202525 |
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author | Wu, Chia-Shan Muthyala, Sai Deepak Venkata Klemashevich, Cory Ufondu, Arinzechukwu Uchenna Menon, Rani Chen, Zheng Devaraj, Sridevi Jayaraman, Arul Sun, Yuxiang |
author_facet | Wu, Chia-Shan Muthyala, Sai Deepak Venkata Klemashevich, Cory Ufondu, Arinzechukwu Uchenna Menon, Rani Chen, Zheng Devaraj, Sridevi Jayaraman, Arul Sun, Yuxiang |
author_sort | Wu, Chia-Shan |
collection | PubMed |
description | The interplay between microbiota and host metabolism plays an important role in health. Here, we examined the relationship between age, gut microbiome and host serum metabolites in male C57BL/6J mice. Fecal microbiome analysis of 3, 6, 18, and 28 months (M) old mice showed that the Firmicutes/Bacteroidetes ratio was highest in the 6M group; the decrease of Firmicutes in the older age groups suggests a reduced capacity of gut microflora to harvest energy from food. We found age-dependent increase in Proteobacteria, which may lead to altered mucus structure more susceptible to bacteria penetration and ultimately increased intestinal inflammation. Metabolomic profiling of polar serum metabolites at fed state in 3, 12, 18 and 28M mice revealed age-associated changes in metabolic cascades involved in tryptophan, purine, amino acids, and nicotinamide metabolism. Correlation analyses showed that nicotinamide decreased with age, while allantoin and guanosine, metabolites in purine metabolism, increased with age. Notably, tryptophan and its microbially derived compounds indole and indole-3-lactic acid significantly decreased with age, while kynurenine increased with age. Together, these results suggest a significant interplay between bacterial and host metabolism, and gut dysbiosis and altered microbial metabolism contribute to aging. |
format | Online Article Text |
id | pubmed-7993679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-79936792021-04-06 Age-dependent remodeling of gut microbiome and host serum metabolome in mice Wu, Chia-Shan Muthyala, Sai Deepak Venkata Klemashevich, Cory Ufondu, Arinzechukwu Uchenna Menon, Rani Chen, Zheng Devaraj, Sridevi Jayaraman, Arul Sun, Yuxiang Aging (Albany NY) Research Paper The interplay between microbiota and host metabolism plays an important role in health. Here, we examined the relationship between age, gut microbiome and host serum metabolites in male C57BL/6J mice. Fecal microbiome analysis of 3, 6, 18, and 28 months (M) old mice showed that the Firmicutes/Bacteroidetes ratio was highest in the 6M group; the decrease of Firmicutes in the older age groups suggests a reduced capacity of gut microflora to harvest energy from food. We found age-dependent increase in Proteobacteria, which may lead to altered mucus structure more susceptible to bacteria penetration and ultimately increased intestinal inflammation. Metabolomic profiling of polar serum metabolites at fed state in 3, 12, 18 and 28M mice revealed age-associated changes in metabolic cascades involved in tryptophan, purine, amino acids, and nicotinamide metabolism. Correlation analyses showed that nicotinamide decreased with age, while allantoin and guanosine, metabolites in purine metabolism, increased with age. Notably, tryptophan and its microbially derived compounds indole and indole-3-lactic acid significantly decreased with age, while kynurenine increased with age. Together, these results suggest a significant interplay between bacterial and host metabolism, and gut dysbiosis and altered microbial metabolism contribute to aging. Impact Journals 2021-02-17 /pmc/articles/PMC7993679/ /pubmed/33612480 http://dx.doi.org/10.18632/aging.202525 Text en Copyright: © 2021 Wu et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Wu, Chia-Shan Muthyala, Sai Deepak Venkata Klemashevich, Cory Ufondu, Arinzechukwu Uchenna Menon, Rani Chen, Zheng Devaraj, Sridevi Jayaraman, Arul Sun, Yuxiang Age-dependent remodeling of gut microbiome and host serum metabolome in mice |
title | Age-dependent remodeling of gut microbiome and host serum metabolome in mice |
title_full | Age-dependent remodeling of gut microbiome and host serum metabolome in mice |
title_fullStr | Age-dependent remodeling of gut microbiome and host serum metabolome in mice |
title_full_unstemmed | Age-dependent remodeling of gut microbiome and host serum metabolome in mice |
title_short | Age-dependent remodeling of gut microbiome and host serum metabolome in mice |
title_sort | age-dependent remodeling of gut microbiome and host serum metabolome in mice |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7993679/ https://www.ncbi.nlm.nih.gov/pubmed/33612480 http://dx.doi.org/10.18632/aging.202525 |
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