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Host genotype and exercise exhibit species-level selection for members of the gut bacterial communities in the mouse digestive system
The mammalian gut microbiome can potentially impact host health and disease state. It is known that the mouse-genome, eating-behavior, and exercise-status promotes higher taxonomic rank-level alterations (e.g. family to phyla-level) of the gut microbiota. Here, host genotype or activity status was i...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7265280/ https://www.ncbi.nlm.nih.gov/pubmed/32488198 http://dx.doi.org/10.1038/s41598-020-65740-4 |
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author | Dowden, R. A. McGuinness, L. R. Wisniewski, P. J. Campbell, S. C. Guers, J. J. Oydanich, M. Vatner, S. F. Häggblom, M. M. Kerkhof, L. J. |
author_facet | Dowden, R. A. McGuinness, L. R. Wisniewski, P. J. Campbell, S. C. Guers, J. J. Oydanich, M. Vatner, S. F. Häggblom, M. M. Kerkhof, L. J. |
author_sort | Dowden, R. A. |
collection | PubMed |
description | The mammalian gut microbiome can potentially impact host health and disease state. It is known that the mouse-genome, eating-behavior, and exercise-status promotes higher taxonomic rank-level alterations (e.g. family to phyla-level) of the gut microbiota. Here, host genotype or activity status was investigated to determine if selection of individual bacterial species or strains could be discerned within the murine digestive system. For this study, the fecal bacterial community of adenylyl cyclase 5 knock-out (AC5KO, n = 7) mice or their wild-type (WT, n = 10) littermates under exercise or sedentary conditions were profiled by sequencing rRNA operons. AC5KO mice were chosen since this genotype displays enhanced longevity/exercise capacity and protects against cardiovascular/metabolic disease. Profiling of rRNA operons using the Oxford MinION yielded 65,706 2-D sequences (after size selection of 3.7–5.7 kb) which were screened against an NCBI 16S rRNA gene database. These sequences were binned into 1,566 different best BLAST hits (BBHs) and counted for each mouse sample. Non-metric multidimensional scaling (NMDS) of the gut microbial community demonstrated clustering by physical activity (p = 0.001) but not by host genotype. Additionally, sequence similarity and phylogenetic analysis demonstrated that different bacterial species (closely related to Muribaculum intestinale and Parasutterella excrementihominis) inhabit AC5KO or WT mice depending on activity status. Other bacterial species of the gut microbiota did not follow such patterning (e.g. Turicibacter sanguinis and Turicimonas muris). Our results support the need of improved taxonomic resolution for better characterization of bacterial communities to deepen our understanding of the role of the gut microbiome on host health. |
format | Online Article Text |
id | pubmed-7265280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72652802020-06-05 Host genotype and exercise exhibit species-level selection for members of the gut bacterial communities in the mouse digestive system Dowden, R. A. McGuinness, L. R. Wisniewski, P. J. Campbell, S. C. Guers, J. J. Oydanich, M. Vatner, S. F. Häggblom, M. M. Kerkhof, L. J. Sci Rep Article The mammalian gut microbiome can potentially impact host health and disease state. It is known that the mouse-genome, eating-behavior, and exercise-status promotes higher taxonomic rank-level alterations (e.g. family to phyla-level) of the gut microbiota. Here, host genotype or activity status was investigated to determine if selection of individual bacterial species or strains could be discerned within the murine digestive system. For this study, the fecal bacterial community of adenylyl cyclase 5 knock-out (AC5KO, n = 7) mice or their wild-type (WT, n = 10) littermates under exercise or sedentary conditions were profiled by sequencing rRNA operons. AC5KO mice were chosen since this genotype displays enhanced longevity/exercise capacity and protects against cardiovascular/metabolic disease. Profiling of rRNA operons using the Oxford MinION yielded 65,706 2-D sequences (after size selection of 3.7–5.7 kb) which were screened against an NCBI 16S rRNA gene database. These sequences were binned into 1,566 different best BLAST hits (BBHs) and counted for each mouse sample. Non-metric multidimensional scaling (NMDS) of the gut microbial community demonstrated clustering by physical activity (p = 0.001) but not by host genotype. Additionally, sequence similarity and phylogenetic analysis demonstrated that different bacterial species (closely related to Muribaculum intestinale and Parasutterella excrementihominis) inhabit AC5KO or WT mice depending on activity status. Other bacterial species of the gut microbiota did not follow such patterning (e.g. Turicibacter sanguinis and Turicimonas muris). Our results support the need of improved taxonomic resolution for better characterization of bacterial communities to deepen our understanding of the role of the gut microbiome on host health. Nature Publishing Group UK 2020-06-02 /pmc/articles/PMC7265280/ /pubmed/32488198 http://dx.doi.org/10.1038/s41598-020-65740-4 Text en © The Author(s) 2020 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 Dowden, R. A. McGuinness, L. R. Wisniewski, P. J. Campbell, S. C. Guers, J. J. Oydanich, M. Vatner, S. F. Häggblom, M. M. Kerkhof, L. J. Host genotype and exercise exhibit species-level selection for members of the gut bacterial communities in the mouse digestive system |
title | Host genotype and exercise exhibit species-level selection for members of the gut bacterial communities in the mouse digestive system |
title_full | Host genotype and exercise exhibit species-level selection for members of the gut bacterial communities in the mouse digestive system |
title_fullStr | Host genotype and exercise exhibit species-level selection for members of the gut bacterial communities in the mouse digestive system |
title_full_unstemmed | Host genotype and exercise exhibit species-level selection for members of the gut bacterial communities in the mouse digestive system |
title_short | Host genotype and exercise exhibit species-level selection for members of the gut bacterial communities in the mouse digestive system |
title_sort | host genotype and exercise exhibit species-level selection for members of the gut bacterial communities in the mouse digestive system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7265280/ https://www.ncbi.nlm.nih.gov/pubmed/32488198 http://dx.doi.org/10.1038/s41598-020-65740-4 |
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