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A model for the role of gut bacteria in the development of autoimmunity for type 1 diabetes
Several lines of evidence suggest a role for the gut microbiome in type 1 diabetes. Treating diabetes-prone rodents with probiotics or antibiotics prevents the development of the disorder. Diabetes-prone rodents also have a distinctly different gut microbiome compared with healthy rodents. Recent st...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4473028/ https://www.ncbi.nlm.nih.gov/pubmed/25957231 http://dx.doi.org/10.1007/s00125-015-3614-8 |
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author | Davis-Richardson, Austin G. Triplett, Eric W. |
author_facet | Davis-Richardson, Austin G. Triplett, Eric W. |
author_sort | Davis-Richardson, Austin G. |
collection | PubMed |
description | Several lines of evidence suggest a role for the gut microbiome in type 1 diabetes. Treating diabetes-prone rodents with probiotics or antibiotics prevents the development of the disorder. Diabetes-prone rodents also have a distinctly different gut microbiome compared with healthy rodents. Recent studies in children with a high genetic risk for type 1 diabetes demonstrate significant differences in the gut microbiome between children who develop autoimmunity for the disease and those who remain healthy. However, the differences in microbiome composition between autoimmune and healthy children are not consistent across all studies because of the strong environmental influences on microbiome composition, particularly diet and geography. Controlling confounding factors of microbiome composition uncovers bacterial associations with disease. For example, in a human cohort from a single Finnish city where geography is confined, a strong association between one dominant bacterial species, Bacteroides dorei, and type 1 diabetes was discovered (Davis-Richardson et al. Front Microbiol2014;5:678). Beyond this, recent DNA methylation analyses suggest that a thorough epigenetic analysis of the gut microbiome may be warranted. These studies suggest a testable model whereby a diet high in fat and gluten and low in resistant starch may be the primary driver of gut dysbiosis. This dysbiosis may cause a lack of butyrate production by gut bacteria, which, in turn, leads to the development of a permeable gut followed by autoimmunity. The bacterial community responsible for these changes in butyrate production may vary around the world, but bacteria of the genus Bacteroides are thought to play a key role. |
format | Online Article Text |
id | pubmed-4473028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-44730282015-06-22 A model for the role of gut bacteria in the development of autoimmunity for type 1 diabetes Davis-Richardson, Austin G. Triplett, Eric W. Diabetologia Review Several lines of evidence suggest a role for the gut microbiome in type 1 diabetes. Treating diabetes-prone rodents with probiotics or antibiotics prevents the development of the disorder. Diabetes-prone rodents also have a distinctly different gut microbiome compared with healthy rodents. Recent studies in children with a high genetic risk for type 1 diabetes demonstrate significant differences in the gut microbiome between children who develop autoimmunity for the disease and those who remain healthy. However, the differences in microbiome composition between autoimmune and healthy children are not consistent across all studies because of the strong environmental influences on microbiome composition, particularly diet and geography. Controlling confounding factors of microbiome composition uncovers bacterial associations with disease. For example, in a human cohort from a single Finnish city where geography is confined, a strong association between one dominant bacterial species, Bacteroides dorei, and type 1 diabetes was discovered (Davis-Richardson et al. Front Microbiol2014;5:678). Beyond this, recent DNA methylation analyses suggest that a thorough epigenetic analysis of the gut microbiome may be warranted. These studies suggest a testable model whereby a diet high in fat and gluten and low in resistant starch may be the primary driver of gut dysbiosis. This dysbiosis may cause a lack of butyrate production by gut bacteria, which, in turn, leads to the development of a permeable gut followed by autoimmunity. The bacterial community responsible for these changes in butyrate production may vary around the world, but bacteria of the genus Bacteroides are thought to play a key role. Springer Berlin Heidelberg 2015-05-10 2015 /pmc/articles/PMC4473028/ /pubmed/25957231 http://dx.doi.org/10.1007/s00125-015-3614-8 Text en © The Author(s) 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Review Davis-Richardson, Austin G. Triplett, Eric W. A model for the role of gut bacteria in the development of autoimmunity for type 1 diabetes |
title | A model for the role of gut bacteria in the development of autoimmunity for type 1 diabetes |
title_full | A model for the role of gut bacteria in the development of autoimmunity for type 1 diabetes |
title_fullStr | A model for the role of gut bacteria in the development of autoimmunity for type 1 diabetes |
title_full_unstemmed | A model for the role of gut bacteria in the development of autoimmunity for type 1 diabetes |
title_short | A model for the role of gut bacteria in the development of autoimmunity for type 1 diabetes |
title_sort | model for the role of gut bacteria in the development of autoimmunity for type 1 diabetes |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4473028/ https://www.ncbi.nlm.nih.gov/pubmed/25957231 http://dx.doi.org/10.1007/s00125-015-3614-8 |
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