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Alterations of the Gut Microbiota in Multiple System Atrophy Patients

Multiple system atrophy (MSA) is a fatal neurodegenerative disease, and the pathogenesis is still quite challenging. Emerging evidence has shown that the brain–gut–microbiota axis served a pivotal role in neurological diseases; however, researches utilizing metagenomic sequencing to analyze the alte...

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Autores principales: Wan, Linlin, Zhou, Xin, Wang, Chunrong, Chen, Zhao, Peng, Huirong, Hou, Xuan, Peng, Yun, Wang, Puzhi, Li, Tianjiao, Yuan, Hongyu, Shi, Yuting, Hou, Xiaocan, Xu, Keqin, Xie, Yue, He, Lang, Xia, Kun, Tang, Beisha, Jiang, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6813281/
https://www.ncbi.nlm.nih.gov/pubmed/31680836
http://dx.doi.org/10.3389/fnins.2019.01102
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author Wan, Linlin
Zhou, Xin
Wang, Chunrong
Chen, Zhao
Peng, Huirong
Hou, Xuan
Peng, Yun
Wang, Puzhi
Li, Tianjiao
Yuan, Hongyu
Shi, Yuting
Hou, Xiaocan
Xu, Keqin
Xie, Yue
He, Lang
Xia, Kun
Tang, Beisha
Jiang, Hong
author_facet Wan, Linlin
Zhou, Xin
Wang, Chunrong
Chen, Zhao
Peng, Huirong
Hou, Xuan
Peng, Yun
Wang, Puzhi
Li, Tianjiao
Yuan, Hongyu
Shi, Yuting
Hou, Xiaocan
Xu, Keqin
Xie, Yue
He, Lang
Xia, Kun
Tang, Beisha
Jiang, Hong
author_sort Wan, Linlin
collection PubMed
description Multiple system atrophy (MSA) is a fatal neurodegenerative disease, and the pathogenesis is still quite challenging. Emerging evidence has shown that the brain–gut–microbiota axis served a pivotal role in neurological diseases; however, researches utilizing metagenomic sequencing to analyze the alteration in gut microbiota of MSA patients were quite rare. Here, we carried out metagenomic sequencing in feces of 15 MSA patients and 15 healthy controls, to characterize the alterations in gut microbial composition and function of MSA patients in mainland China. The results showed that gut microbial community of MSA patients was significantly different from healthy controls, characterized by increased genus Akkermansia and species Roseburia hominis, Akkermansia muciniphila, Alistipes onderdonkii, Streptococcus parasanguinis, and Staphylococcus xylosus, while decreased genera Megamonas, Bifidobacterium, Blautia, and Aggregatibacter and species Bacteroides coprocola, Megamonas funiformis, Bifidobacterium pseudocatenulatum, Clostridium nexile, Bacteroides plebeius, and Granulicatella adiacens. Further, functional analysis based on the KEGG database revealed aberrant functional pathways in fecal microbiome of MSA patients. In conclusion, our findings provided evidence for dysbiosis in gut microbiota of Chinese MSA cohorts and helped develop new testable hypotheses on pathophysiology of MSA.
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spelling pubmed-68132812019-11-01 Alterations of the Gut Microbiota in Multiple System Atrophy Patients Wan, Linlin Zhou, Xin Wang, Chunrong Chen, Zhao Peng, Huirong Hou, Xuan Peng, Yun Wang, Puzhi Li, Tianjiao Yuan, Hongyu Shi, Yuting Hou, Xiaocan Xu, Keqin Xie, Yue He, Lang Xia, Kun Tang, Beisha Jiang, Hong Front Neurosci Neuroscience Multiple system atrophy (MSA) is a fatal neurodegenerative disease, and the pathogenesis is still quite challenging. Emerging evidence has shown that the brain–gut–microbiota axis served a pivotal role in neurological diseases; however, researches utilizing metagenomic sequencing to analyze the alteration in gut microbiota of MSA patients were quite rare. Here, we carried out metagenomic sequencing in feces of 15 MSA patients and 15 healthy controls, to characterize the alterations in gut microbial composition and function of MSA patients in mainland China. The results showed that gut microbial community of MSA patients was significantly different from healthy controls, characterized by increased genus Akkermansia and species Roseburia hominis, Akkermansia muciniphila, Alistipes onderdonkii, Streptococcus parasanguinis, and Staphylococcus xylosus, while decreased genera Megamonas, Bifidobacterium, Blautia, and Aggregatibacter and species Bacteroides coprocola, Megamonas funiformis, Bifidobacterium pseudocatenulatum, Clostridium nexile, Bacteroides plebeius, and Granulicatella adiacens. Further, functional analysis based on the KEGG database revealed aberrant functional pathways in fecal microbiome of MSA patients. In conclusion, our findings provided evidence for dysbiosis in gut microbiota of Chinese MSA cohorts and helped develop new testable hypotheses on pathophysiology of MSA. Frontiers Media S.A. 2019-10-18 /pmc/articles/PMC6813281/ /pubmed/31680836 http://dx.doi.org/10.3389/fnins.2019.01102 Text en Copyright © 2019 Wan, Zhou, Wang, Chen, Peng, Hou, Peng, Wang, Li, Yuan, Shi, Hou, Xu, Xie, He, Xia, Tang and Jiang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Wan, Linlin
Zhou, Xin
Wang, Chunrong
Chen, Zhao
Peng, Huirong
Hou, Xuan
Peng, Yun
Wang, Puzhi
Li, Tianjiao
Yuan, Hongyu
Shi, Yuting
Hou, Xiaocan
Xu, Keqin
Xie, Yue
He, Lang
Xia, Kun
Tang, Beisha
Jiang, Hong
Alterations of the Gut Microbiota in Multiple System Atrophy Patients
title Alterations of the Gut Microbiota in Multiple System Atrophy Patients
title_full Alterations of the Gut Microbiota in Multiple System Atrophy Patients
title_fullStr Alterations of the Gut Microbiota in Multiple System Atrophy Patients
title_full_unstemmed Alterations of the Gut Microbiota in Multiple System Atrophy Patients
title_short Alterations of the Gut Microbiota in Multiple System Atrophy Patients
title_sort alterations of the gut microbiota in multiple system atrophy patients
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6813281/
https://www.ncbi.nlm.nih.gov/pubmed/31680836
http://dx.doi.org/10.3389/fnins.2019.01102
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