4.6 Article

Alterations of the Gut Microbiota in Multiple System Atrophy Patients

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FRONTIERS IN NEUROSCIENCE
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fnins.2019.01102

关键词

multiple system atrophy; microbiota; metagenomics; functional pathways; inflammation

资金

  1. National Key Research and Development Program of China [2016YFC0901504, 2016YFC0905100, 2016YFC1306000]
  2. National Natural Science Foundation of China [8177123, 81471156, 81600995]
  3. Key Research and Development Program of Hunan Province [2018SK2092]
  4. Scientific Research Foundation of Health Commission of Hunan Province [B2019183]
  5. Clinical and Rehabilitation Fund of Peking University Weiming Biotech Group [xywm2015I10]

向作者/读者索取更多资源

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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