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The alteration of gut microbiome and metabolism in amyotrophic lateral sclerosis patients
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease accompanied with severe paralysis or even death, while the pathogenesis of ALS is still unclear and no effective therapy exists. The accumulating evidence has indicated the association between gut microbiota and various neurological...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7398913/ https://www.ncbi.nlm.nih.gov/pubmed/32747678 http://dx.doi.org/10.1038/s41598-020-69845-8 |
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author | Zeng, Qianqian Shen, Jie Chen, Kangzhi Zhou, Jinxia Liao, Qiao Lu, Ke Yuan, Jiao Bi, Fangfang |
author_facet | Zeng, Qianqian Shen, Jie Chen, Kangzhi Zhou, Jinxia Liao, Qiao Lu, Ke Yuan, Jiao Bi, Fangfang |
author_sort | Zeng, Qianqian |
collection | PubMed |
description | Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease accompanied with severe paralysis or even death, while the pathogenesis of ALS is still unclear and no effective therapy exists. The accumulating evidence has indicated the association between gut microbiota and various neurological diseases. Thus, to explore the potential role of gut microbiome in ALS, 20 patients diagnosed with probable or definite ALS and 20 healthy controls were enrolled and their fecal excrements were collected. The analysis of fecal community diversity with 16S rDNA sequencing showed an obvious change in microbial structure of ALS patients, where Bacteroidetes at the phylum level and several microbes at the genus level were up-regulated, while Firmicutes at the phylum level and Megamonas at the genus level were down-regulated compared to healthy controls. Additionally, decreased gene function associated with metabolic pathways was observed in ALS patients. The metagenomics further demonstrated the discrepancies in microflora at the species level and relevant metabolites thereof were also revealed when combined with metabolomics. In conclusion, the altered composition of the gut microbiota and metabolic products in ALS patients provided deeper insights into the pathogenesis of ALS, and these biomarkers might be established as potential therapeutic targets which deserve further exploration. |
format | Online Article Text |
id | pubmed-7398913 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73989132020-08-04 The alteration of gut microbiome and metabolism in amyotrophic lateral sclerosis patients Zeng, Qianqian Shen, Jie Chen, Kangzhi Zhou, Jinxia Liao, Qiao Lu, Ke Yuan, Jiao Bi, Fangfang Sci Rep Article Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease accompanied with severe paralysis or even death, while the pathogenesis of ALS is still unclear and no effective therapy exists. The accumulating evidence has indicated the association between gut microbiota and various neurological diseases. Thus, to explore the potential role of gut microbiome in ALS, 20 patients diagnosed with probable or definite ALS and 20 healthy controls were enrolled and their fecal excrements were collected. The analysis of fecal community diversity with 16S rDNA sequencing showed an obvious change in microbial structure of ALS patients, where Bacteroidetes at the phylum level and several microbes at the genus level were up-regulated, while Firmicutes at the phylum level and Megamonas at the genus level were down-regulated compared to healthy controls. Additionally, decreased gene function associated with metabolic pathways was observed in ALS patients. The metagenomics further demonstrated the discrepancies in microflora at the species level and relevant metabolites thereof were also revealed when combined with metabolomics. In conclusion, the altered composition of the gut microbiota and metabolic products in ALS patients provided deeper insights into the pathogenesis of ALS, and these biomarkers might be established as potential therapeutic targets which deserve further exploration. Nature Publishing Group UK 2020-08-03 /pmc/articles/PMC7398913/ /pubmed/32747678 http://dx.doi.org/10.1038/s41598-020-69845-8 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zeng, Qianqian Shen, Jie Chen, Kangzhi Zhou, Jinxia Liao, Qiao Lu, Ke Yuan, Jiao Bi, Fangfang The alteration of gut microbiome and metabolism in amyotrophic lateral sclerosis patients |
title | The alteration of gut microbiome and metabolism in amyotrophic lateral sclerosis patients |
title_full | The alteration of gut microbiome and metabolism in amyotrophic lateral sclerosis patients |
title_fullStr | The alteration of gut microbiome and metabolism in amyotrophic lateral sclerosis patients |
title_full_unstemmed | The alteration of gut microbiome and metabolism in amyotrophic lateral sclerosis patients |
title_short | The alteration of gut microbiome and metabolism in amyotrophic lateral sclerosis patients |
title_sort | alteration of gut microbiome and metabolism in amyotrophic lateral sclerosis patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7398913/ https://www.ncbi.nlm.nih.gov/pubmed/32747678 http://dx.doi.org/10.1038/s41598-020-69845-8 |
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