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Alterations of the human gut microbiome in multiple sclerosis
The gut microbiome plays an important role in immune function and has been implicated in several autoimmune disorders. Here we use 16S rRNA sequencing to investigate the gut microbiome in subjects with multiple sclerosis (MS, n=60) and healthy controls (n=43). Microbiome alterations in MS include in...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931233/ https://www.ncbi.nlm.nih.gov/pubmed/27352007 http://dx.doi.org/10.1038/ncomms12015 |
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author | Jangi, Sushrut Gandhi, Roopali Cox, Laura M. Li, Ning von Glehn, Felipe Yan, Raymond Patel, Bonny Mazzola, Maria Antonietta Liu, Shirong Glanz, Bonnie L. Cook, Sandra Tankou, Stephanie Stuart, Fiona Melo, Kirsy Nejad, Parham Smith, Kathleen Topçuolu, Begüm D. Holden, James Kivisäkk, Pia Chitnis, Tanuja De Jager, Philip L. Quintana, Francisco J. Gerber, Georg K. Bry, Lynn Weiner, Howard L. |
author_facet | Jangi, Sushrut Gandhi, Roopali Cox, Laura M. Li, Ning von Glehn, Felipe Yan, Raymond Patel, Bonny Mazzola, Maria Antonietta Liu, Shirong Glanz, Bonnie L. Cook, Sandra Tankou, Stephanie Stuart, Fiona Melo, Kirsy Nejad, Parham Smith, Kathleen Topçuolu, Begüm D. Holden, James Kivisäkk, Pia Chitnis, Tanuja De Jager, Philip L. Quintana, Francisco J. Gerber, Georg K. Bry, Lynn Weiner, Howard L. |
author_sort | Jangi, Sushrut |
collection | PubMed |
description | The gut microbiome plays an important role in immune function and has been implicated in several autoimmune disorders. Here we use 16S rRNA sequencing to investigate the gut microbiome in subjects with multiple sclerosis (MS, n=60) and healthy controls (n=43). Microbiome alterations in MS include increases in Methanobrevibacter and Akkermansia and decreases in Butyricimonas, and correlate with variations in the expression of genes involved in dendritic cell maturation, interferon signalling and NF-kB signalling pathways in circulating T cells and monocytes. Patients on disease-modifying treatment show increased abundances of Prevotella and Sutterella, and decreased Sarcina, compared with untreated patients. MS patients of a second cohort show elevated breath methane compared with controls, consistent with our observation of increased gut Methanobrevibacter in MS in the first cohort. Further study is required to assess whether the observed alterations in the gut microbiome play a role in, or are a consequence of, MS pathogenesis. |
format | Online Article Text |
id | pubmed-4931233 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49312332016-07-12 Alterations of the human gut microbiome in multiple sclerosis Jangi, Sushrut Gandhi, Roopali Cox, Laura M. Li, Ning von Glehn, Felipe Yan, Raymond Patel, Bonny Mazzola, Maria Antonietta Liu, Shirong Glanz, Bonnie L. Cook, Sandra Tankou, Stephanie Stuart, Fiona Melo, Kirsy Nejad, Parham Smith, Kathleen Topçuolu, Begüm D. Holden, James Kivisäkk, Pia Chitnis, Tanuja De Jager, Philip L. Quintana, Francisco J. Gerber, Georg K. Bry, Lynn Weiner, Howard L. Nat Commun Article The gut microbiome plays an important role in immune function and has been implicated in several autoimmune disorders. Here we use 16S rRNA sequencing to investigate the gut microbiome in subjects with multiple sclerosis (MS, n=60) and healthy controls (n=43). Microbiome alterations in MS include increases in Methanobrevibacter and Akkermansia and decreases in Butyricimonas, and correlate with variations in the expression of genes involved in dendritic cell maturation, interferon signalling and NF-kB signalling pathways in circulating T cells and monocytes. Patients on disease-modifying treatment show increased abundances of Prevotella and Sutterella, and decreased Sarcina, compared with untreated patients. MS patients of a second cohort show elevated breath methane compared with controls, consistent with our observation of increased gut Methanobrevibacter in MS in the first cohort. Further study is required to assess whether the observed alterations in the gut microbiome play a role in, or are a consequence of, MS pathogenesis. Nature Publishing Group 2016-06-28 /pmc/articles/PMC4931233/ /pubmed/27352007 http://dx.doi.org/10.1038/ncomms12015 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Jangi, Sushrut Gandhi, Roopali Cox, Laura M. Li, Ning von Glehn, Felipe Yan, Raymond Patel, Bonny Mazzola, Maria Antonietta Liu, Shirong Glanz, Bonnie L. Cook, Sandra Tankou, Stephanie Stuart, Fiona Melo, Kirsy Nejad, Parham Smith, Kathleen Topçuolu, Begüm D. Holden, James Kivisäkk, Pia Chitnis, Tanuja De Jager, Philip L. Quintana, Francisco J. Gerber, Georg K. Bry, Lynn Weiner, Howard L. Alterations of the human gut microbiome in multiple sclerosis |
title | Alterations of the human gut microbiome in multiple sclerosis |
title_full | Alterations of the human gut microbiome in multiple sclerosis |
title_fullStr | Alterations of the human gut microbiome in multiple sclerosis |
title_full_unstemmed | Alterations of the human gut microbiome in multiple sclerosis |
title_short | Alterations of the human gut microbiome in multiple sclerosis |
title_sort | alterations of the human gut microbiome in multiple sclerosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931233/ https://www.ncbi.nlm.nih.gov/pubmed/27352007 http://dx.doi.org/10.1038/ncomms12015 |
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