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Intestinal mucosal microbiota composition of patients with acquired immune deficiency syndrome in Guangzhou, China

Acquired immune deficiency syndrome, caused by the human immunodeficiency virus (HIV), has been associated with intestinal dysbiosis, which includes an increase in the number of mucosa-associated pathobionts. In the present study, the intestinal mucosal microbiota patterns of HIV-infected patients w...

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Autores principales: Xu, Haoming, Ou, Zhitao, Zhou, Yongjian, Li, Yingfei, Huang, Hongli, Zhao, Hailan, Xu, Jing, Luo, Meijuan, Zhou, Youlian, Nie, Yuqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7918403/
https://www.ncbi.nlm.nih.gov/pubmed/33680113
http://dx.doi.org/10.3892/etm.2021.9822
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author Xu, Haoming
Ou, Zhitao
Zhou, Yongjian
Li, Yingfei
Huang, Hongli
Zhao, Hailan
Xu, Jing
Luo, Meijuan
Zhou, Youlian
Nie, Yuqiang
author_facet Xu, Haoming
Ou, Zhitao
Zhou, Yongjian
Li, Yingfei
Huang, Hongli
Zhao, Hailan
Xu, Jing
Luo, Meijuan
Zhou, Youlian
Nie, Yuqiang
author_sort Xu, Haoming
collection PubMed
description Acquired immune deficiency syndrome, caused by the human immunodeficiency virus (HIV), has been associated with intestinal dysbiosis, which includes an increase in the number of mucosa-associated pathobionts. In the present study, the intestinal mucosal microbiota patterns of HIV-infected patients were compared with those of healthy individuals in a population from Guangzhou, China. The gut microbiota of intestinal mucosal samples from 12 patients with HIV (transmission routes included sex and intravenous drug abuse) was compared with that of 12 healthy age- and sex-matched controls. Gut microbial communities were profiled via sequencing of the bacterial 16S ribosomal RNA genes. Dysbiosis in HIV-infected individuals was characterized by decreased α-diversity, decreased levels of Firmicutes and increased levels of Proteobacteria. Furthermore, low mean counts of Lachnoclostridium, Roseburia, Thauera, Dorea and Roseburia inulinivorans, and high mean counts of Halomonas and Shewanella bacteria, were indicated to be HIV-associated mucosal bacterial alterations. The relative abundance of Fusobacterium and Lachnoclostridium was significantly decreased, while that of Halomonas and Shewanella was significantly increased in patients with sexually transmitted HIV-infection compared with healthy controls. Alterations of the gut microbiota during HIV infection were also indicated to be associated with the route of HIV transmission. Certain bacteria may be potential biomarkers for HIV infection in patients from Guangzhou, China.
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spelling pubmed-79184032021-03-05 Intestinal mucosal microbiota composition of patients with acquired immune deficiency syndrome in Guangzhou, China Xu, Haoming Ou, Zhitao Zhou, Yongjian Li, Yingfei Huang, Hongli Zhao, Hailan Xu, Jing Luo, Meijuan Zhou, Youlian Nie, Yuqiang Exp Ther Med Articles Acquired immune deficiency syndrome, caused by the human immunodeficiency virus (HIV), has been associated with intestinal dysbiosis, which includes an increase in the number of mucosa-associated pathobionts. In the present study, the intestinal mucosal microbiota patterns of HIV-infected patients were compared with those of healthy individuals in a population from Guangzhou, China. The gut microbiota of intestinal mucosal samples from 12 patients with HIV (transmission routes included sex and intravenous drug abuse) was compared with that of 12 healthy age- and sex-matched controls. Gut microbial communities were profiled via sequencing of the bacterial 16S ribosomal RNA genes. Dysbiosis in HIV-infected individuals was characterized by decreased α-diversity, decreased levels of Firmicutes and increased levels of Proteobacteria. Furthermore, low mean counts of Lachnoclostridium, Roseburia, Thauera, Dorea and Roseburia inulinivorans, and high mean counts of Halomonas and Shewanella bacteria, were indicated to be HIV-associated mucosal bacterial alterations. The relative abundance of Fusobacterium and Lachnoclostridium was significantly decreased, while that of Halomonas and Shewanella was significantly increased in patients with sexually transmitted HIV-infection compared with healthy controls. Alterations of the gut microbiota during HIV infection were also indicated to be associated with the route of HIV transmission. Certain bacteria may be potential biomarkers for HIV infection in patients from Guangzhou, China. D.A. Spandidos 2021-04 2021-02-24 /pmc/articles/PMC7918403/ /pubmed/33680113 http://dx.doi.org/10.3892/etm.2021.9822 Text en Copyright: © Xu et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Xu, Haoming
Ou, Zhitao
Zhou, Yongjian
Li, Yingfei
Huang, Hongli
Zhao, Hailan
Xu, Jing
Luo, Meijuan
Zhou, Youlian
Nie, Yuqiang
Intestinal mucosal microbiota composition of patients with acquired immune deficiency syndrome in Guangzhou, China
title Intestinal mucosal microbiota composition of patients with acquired immune deficiency syndrome in Guangzhou, China
title_full Intestinal mucosal microbiota composition of patients with acquired immune deficiency syndrome in Guangzhou, China
title_fullStr Intestinal mucosal microbiota composition of patients with acquired immune deficiency syndrome in Guangzhou, China
title_full_unstemmed Intestinal mucosal microbiota composition of patients with acquired immune deficiency syndrome in Guangzhou, China
title_short Intestinal mucosal microbiota composition of patients with acquired immune deficiency syndrome in Guangzhou, China
title_sort intestinal mucosal microbiota composition of patients with acquired immune deficiency syndrome in guangzhou, china
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7918403/
https://www.ncbi.nlm.nih.gov/pubmed/33680113
http://dx.doi.org/10.3892/etm.2021.9822
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