Alterations in intestinal microbiota diversity, composition, and function in patients with sarcopenia
Abstract 16S rRNA sequencing of human fecal samples has been tremendously successful in identifying microbiome changes associated with both aging and disease. A number of studies have described microbial alterations corresponding to physical frailty and nursing home residence among aging individuals...
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doaj-ee5ab244d47b49f2abf3fb935bef0b2b2021-03-11T12:13:27ZengNature Publishing GroupScientific Reports2045-23222021-02-0111111410.1038/s41598-021-84031-0Alterations in intestinal microbiota diversity, composition, and function in patients with sarcopeniaLin Kang0Pengtao Li1Danyang Wang2Taihao Wang3Dong Hao4Xuan Qu5Department of Geriatrics, Peking Union Medical College HospitalAllwegene Technology Inc.Department of Geriatrics, Urumqi Friendship HospitalDepartment of Geriatrics Centre, Hainan General HospitalDepartment of Geriatrics, Liaocheng People’s HospitalDepartment of Geriatrics, Peking Union Medical College HospitalAbstract 16S rRNA sequencing of human fecal samples has been tremendously successful in identifying microbiome changes associated with both aging and disease. A number of studies have described microbial alterations corresponding to physical frailty and nursing home residence among aging individuals. A gut-muscle axis through which the microbiome influences skeletal muscle growth/function has been hypothesized. However, the microbiome has yet to be examined in sarcopenia. Here, we collected fecal samples of 60 healthy controls (CON) and 27 sarcopenic (Case)/possibly sarcopenic (preCase) individuals and analyzed the intestinal microbiota using 16S rRNA sequencing. We observed an overall reduction in microbial diversity in Case and preCase samples. The genera Lachnospira, Fusicantenibacter, Roseburia, Eubacterium, and Lachnoclostridium—known butyrate producers—were significantly less abundant in Case and preCase subjects while Lactobacillus was more abundant. Functional pathways underrepresented in Case subjects included numerous transporters and phenylalanine, tyrosine, and tryptophan biosynthesis suggesting that protein processing and nutrient transport may be impaired. In contrast, lipopolysaccharide biosynthesis was overrepresented in Case and PreCase subjects suggesting that sarcopenia is associated with a pro-inflammatory metagenome. These analyses demonstrate structural and functional alterations in the intestinal microbiota that may contribute to loss of skeletal muscle mass and function in sarcopenia.https://doi.org/10.1038/s41598-021-84031-0 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Lin Kang Pengtao Li Danyang Wang Taihao Wang Dong Hao Xuan Qu |
spellingShingle |
Lin Kang Pengtao Li Danyang Wang Taihao Wang Dong Hao Xuan Qu Alterations in intestinal microbiota diversity, composition, and function in patients with sarcopenia Scientific Reports |
author_facet |
Lin Kang Pengtao Li Danyang Wang Taihao Wang Dong Hao Xuan Qu |
author_sort |
Lin Kang |
title |
Alterations in intestinal microbiota diversity, composition, and function in patients with sarcopenia |
title_short |
Alterations in intestinal microbiota diversity, composition, and function in patients with sarcopenia |
title_full |
Alterations in intestinal microbiota diversity, composition, and function in patients with sarcopenia |
title_fullStr |
Alterations in intestinal microbiota diversity, composition, and function in patients with sarcopenia |
title_full_unstemmed |
Alterations in intestinal microbiota diversity, composition, and function in patients with sarcopenia |
title_sort |
alterations in intestinal microbiota diversity, composition, and function in patients with sarcopenia |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-02-01 |
description |
Abstract 16S rRNA sequencing of human fecal samples has been tremendously successful in identifying microbiome changes associated with both aging and disease. A number of studies have described microbial alterations corresponding to physical frailty and nursing home residence among aging individuals. A gut-muscle axis through which the microbiome influences skeletal muscle growth/function has been hypothesized. However, the microbiome has yet to be examined in sarcopenia. Here, we collected fecal samples of 60 healthy controls (CON) and 27 sarcopenic (Case)/possibly sarcopenic (preCase) individuals and analyzed the intestinal microbiota using 16S rRNA sequencing. We observed an overall reduction in microbial diversity in Case and preCase samples. The genera Lachnospira, Fusicantenibacter, Roseburia, Eubacterium, and Lachnoclostridium—known butyrate producers—were significantly less abundant in Case and preCase subjects while Lactobacillus was more abundant. Functional pathways underrepresented in Case subjects included numerous transporters and phenylalanine, tyrosine, and tryptophan biosynthesis suggesting that protein processing and nutrient transport may be impaired. In contrast, lipopolysaccharide biosynthesis was overrepresented in Case and PreCase subjects suggesting that sarcopenia is associated with a pro-inflammatory metagenome. These analyses demonstrate structural and functional alterations in the intestinal microbiota that may contribute to loss of skeletal muscle mass and function in sarcopenia. |
url |
https://doi.org/10.1038/s41598-021-84031-0 |
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