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Possible correlation between gut microbiota and immunity among healthy middle-aged and elderly people in southwest China

BACKGROUND: The present study was conducted to investigate the possible association between gut microbes and immunity among healthy middle-aged and elderly individuals in southwest China. A total of 148 healthy adults aged ≥ 50 years were divided into two age groups: middle-aged group (50–59 years;...

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Autores principales: Shen, Xi, Miao, Junjie, Wan, Qun, Wang, Shuyue, Li, Ming, Pu, Fangfang, Wang, Guoqing, Qian, Wei, Yu, Qian, Marotta, Francesco, He, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806246/
https://www.ncbi.nlm.nih.gov/pubmed/29449892
http://dx.doi.org/10.1186/s13099-018-0231-3
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author Shen, Xi
Miao, Junjie
Wan, Qun
Wang, Shuyue
Li, Ming
Pu, Fangfang
Wang, Guoqing
Qian, Wei
Yu, Qian
Marotta, Francesco
He, Fang
author_facet Shen, Xi
Miao, Junjie
Wan, Qun
Wang, Shuyue
Li, Ming
Pu, Fangfang
Wang, Guoqing
Qian, Wei
Yu, Qian
Marotta, Francesco
He, Fang
author_sort Shen, Xi
collection PubMed
description BACKGROUND: The present study was conducted to investigate the possible association between gut microbes and immunity among healthy middle-aged and elderly individuals in southwest China. A total of 148 healthy adults aged ≥ 50 years were divided into two age groups: middle-aged group (50–59 years; n = 67, 54.13 ± 3.32) and elderly group (≥ 60 years; n = 81, 64.70 ± 3.93). Blood samples were collected to measure serum immune and biochemical indices. Gut microbiota compositions of the groups were characterized on the basis of faecal DNA using 16S rRNA gene sequencing. RESULTS: Among the detected gut microbes, the presence of Alistipes was negatively correlated with age in both groups. In the middle-aged group, age was negatively correlated with the presence of Desulfovibrio and Faecalibacterium. In the elderly group, Coprococcus was present at significantly higher levels; age was negatively correlated with the presence of Lachnobacterium, Oxalobacter and the Chao index, whereas positively correlated with the presence of Sutterella. In the middle-aged group, the presence of Bacteroidetes was positively correlated with serum immunoglobulin G (IgG) levels and the percent of CD8(+) T cells and negatively correlated with the CD4(+)/CD8(+) ratio; the presence of Firmicutes was negatively correlated with IgM levels; Bacteroidetes/Firmicutes ratio was positively correlated with IgG and IgM levels and Simpson index was negatively correlated with the percent of CD8(+) T cells and positively correlated with CD4(+)/CD8(+) ratio. In the elderly group, the presence of Verrucomicrobia (identified as genus Akkermansia) was positively correlated with IgA levels and the percent of CD8(+) T cells and negatively correlated with the percent of CD4(+) T cells and CD4(+)/CD8(+) ratio; the Chao index and observed species were positively correlated with IgA levels. CONCLUSIONS: These results indicated that ageing could significantly correlate with the composition of gut microbiota in terms of quantity and quality. Changes in gut microbiota caused by ageing, characterized by decreased Bacteroidetes levels, might be associated with immunosenescence among healthy middle-aged and elderly people in southwest China. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13099-018-0231-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-58062462018-02-15 Possible correlation between gut microbiota and immunity among healthy middle-aged and elderly people in southwest China Shen, Xi Miao, Junjie Wan, Qun Wang, Shuyue Li, Ming Pu, Fangfang Wang, Guoqing Qian, Wei Yu, Qian Marotta, Francesco He, Fang Gut Pathog Research BACKGROUND: The present study was conducted to investigate the possible association between gut microbes and immunity among healthy middle-aged and elderly individuals in southwest China. A total of 148 healthy adults aged ≥ 50 years were divided into two age groups: middle-aged group (50–59 years; n = 67, 54.13 ± 3.32) and elderly group (≥ 60 years; n = 81, 64.70 ± 3.93). Blood samples were collected to measure serum immune and biochemical indices. Gut microbiota compositions of the groups were characterized on the basis of faecal DNA using 16S rRNA gene sequencing. RESULTS: Among the detected gut microbes, the presence of Alistipes was negatively correlated with age in both groups. In the middle-aged group, age was negatively correlated with the presence of Desulfovibrio and Faecalibacterium. In the elderly group, Coprococcus was present at significantly higher levels; age was negatively correlated with the presence of Lachnobacterium, Oxalobacter and the Chao index, whereas positively correlated with the presence of Sutterella. In the middle-aged group, the presence of Bacteroidetes was positively correlated with serum immunoglobulin G (IgG) levels and the percent of CD8(+) T cells and negatively correlated with the CD4(+)/CD8(+) ratio; the presence of Firmicutes was negatively correlated with IgM levels; Bacteroidetes/Firmicutes ratio was positively correlated with IgG and IgM levels and Simpson index was negatively correlated with the percent of CD8(+) T cells and positively correlated with CD4(+)/CD8(+) ratio. In the elderly group, the presence of Verrucomicrobia (identified as genus Akkermansia) was positively correlated with IgA levels and the percent of CD8(+) T cells and negatively correlated with the percent of CD4(+) T cells and CD4(+)/CD8(+) ratio; the Chao index and observed species were positively correlated with IgA levels. CONCLUSIONS: These results indicated that ageing could significantly correlate with the composition of gut microbiota in terms of quantity and quality. Changes in gut microbiota caused by ageing, characterized by decreased Bacteroidetes levels, might be associated with immunosenescence among healthy middle-aged and elderly people in southwest China. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13099-018-0231-3) contains supplementary material, which is available to authorized users. BioMed Central 2018-02-09 /pmc/articles/PMC5806246/ /pubmed/29449892 http://dx.doi.org/10.1186/s13099-018-0231-3 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Shen, Xi
Miao, Junjie
Wan, Qun
Wang, Shuyue
Li, Ming
Pu, Fangfang
Wang, Guoqing
Qian, Wei
Yu, Qian
Marotta, Francesco
He, Fang
Possible correlation between gut microbiota and immunity among healthy middle-aged and elderly people in southwest China
title Possible correlation between gut microbiota and immunity among healthy middle-aged and elderly people in southwest China
title_full Possible correlation between gut microbiota and immunity among healthy middle-aged and elderly people in southwest China
title_fullStr Possible correlation between gut microbiota and immunity among healthy middle-aged and elderly people in southwest China
title_full_unstemmed Possible correlation between gut microbiota and immunity among healthy middle-aged and elderly people in southwest China
title_short Possible correlation between gut microbiota and immunity among healthy middle-aged and elderly people in southwest China
title_sort possible correlation between gut microbiota and immunity among healthy middle-aged and elderly people in southwest china
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806246/
https://www.ncbi.nlm.nih.gov/pubmed/29449892
http://dx.doi.org/10.1186/s13099-018-0231-3
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