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Gut microbial dysbiosis in individuals with Sjögren’s syndrome
BACKGROUND: Autoimmune diseases have been associated with changes in the gut microbiome. In this study, the gut microbiome was evaluated in individuals with dry eye and bacterial compositions were correlated to dry eye (DE) measures. We prospectively included 13 individuals with who met full criteri...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7158097/ https://www.ncbi.nlm.nih.gov/pubmed/32293464 http://dx.doi.org/10.1186/s12934-020-01348-7 |
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author | Mendez, Roberto Watane, Arjun Farhangi, Monika Cavuoto, Kara M. Leith, Tom Budree, Shrish Galor, Anat Banerjee, Santanu |
author_facet | Mendez, Roberto Watane, Arjun Farhangi, Monika Cavuoto, Kara M. Leith, Tom Budree, Shrish Galor, Anat Banerjee, Santanu |
author_sort | Mendez, Roberto |
collection | PubMed |
description | BACKGROUND: Autoimmune diseases have been associated with changes in the gut microbiome. In this study, the gut microbiome was evaluated in individuals with dry eye and bacterial compositions were correlated to dry eye (DE) measures. We prospectively included 13 individuals with who met full criteria for Sjögren’s (SDE) and 8 individuals with features of Sjögren’s but who did not meet full criteria (NDE) for a total of 21 cases as compared to 21 healthy controls. Stool was analyzed by 16S pyrosequencing, and associations between bacterial classes and DE symptoms and signs were examined. RESULTS: Results showed that Firmicutes was the dominant phylum in the gut, comprising 40–60% of all phyla. On a phyla level, subjects with DE (SDE and NDE) had depletion of Firmicutes (1.1-fold) and an expansion of Proteobacteria (3.0-fold), Actinobacteria (1.7-fold), and Bacteroidetes (1.3-fold) compared to controls. Shannon’s diversity index showed no differences between groups with respect to the numbers of different operational taxonomic units (OTUs) encountered (diversity) and the instances these unique OTUs were sampled (evenness). On the other hand, Faith’s phylogenetic diversity showed increased diversity in cases vs controls, which reached significance when comparing SDE and controls (13.57 ± 0.89 and 10.96 ± 0.76, p = 0.02). Using Principle Co-ordinate Analysis, qualitative differences in microbial composition were noted with differential clustering of cases and controls. Dimensionality reduction and clustering of complex microbial data further showed differences between the three groups, with regard to microbial composition, association and clustering. Finally, differences in certain classes of bacteria were associated with DE symptoms and signs. CONCLUSIONS: In conclusion, individuals with DE had gut microbiome alterations as compared to healthy controls. Certain classes of bacteria were associated with DE measures. |
format | Online Article Text |
id | pubmed-7158097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-71580972020-04-21 Gut microbial dysbiosis in individuals with Sjögren’s syndrome Mendez, Roberto Watane, Arjun Farhangi, Monika Cavuoto, Kara M. Leith, Tom Budree, Shrish Galor, Anat Banerjee, Santanu Microb Cell Fact Research BACKGROUND: Autoimmune diseases have been associated with changes in the gut microbiome. In this study, the gut microbiome was evaluated in individuals with dry eye and bacterial compositions were correlated to dry eye (DE) measures. We prospectively included 13 individuals with who met full criteria for Sjögren’s (SDE) and 8 individuals with features of Sjögren’s but who did not meet full criteria (NDE) for a total of 21 cases as compared to 21 healthy controls. Stool was analyzed by 16S pyrosequencing, and associations between bacterial classes and DE symptoms and signs were examined. RESULTS: Results showed that Firmicutes was the dominant phylum in the gut, comprising 40–60% of all phyla. On a phyla level, subjects with DE (SDE and NDE) had depletion of Firmicutes (1.1-fold) and an expansion of Proteobacteria (3.0-fold), Actinobacteria (1.7-fold), and Bacteroidetes (1.3-fold) compared to controls. Shannon’s diversity index showed no differences between groups with respect to the numbers of different operational taxonomic units (OTUs) encountered (diversity) and the instances these unique OTUs were sampled (evenness). On the other hand, Faith’s phylogenetic diversity showed increased diversity in cases vs controls, which reached significance when comparing SDE and controls (13.57 ± 0.89 and 10.96 ± 0.76, p = 0.02). Using Principle Co-ordinate Analysis, qualitative differences in microbial composition were noted with differential clustering of cases and controls. Dimensionality reduction and clustering of complex microbial data further showed differences between the three groups, with regard to microbial composition, association and clustering. Finally, differences in certain classes of bacteria were associated with DE symptoms and signs. CONCLUSIONS: In conclusion, individuals with DE had gut microbiome alterations as compared to healthy controls. Certain classes of bacteria were associated with DE measures. BioMed Central 2020-04-15 /pmc/articles/PMC7158097/ /pubmed/32293464 http://dx.doi.org/10.1186/s12934-020-01348-7 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Mendez, Roberto Watane, Arjun Farhangi, Monika Cavuoto, Kara M. Leith, Tom Budree, Shrish Galor, Anat Banerjee, Santanu Gut microbial dysbiosis in individuals with Sjögren’s syndrome |
title | Gut microbial dysbiosis in individuals with Sjögren’s syndrome |
title_full | Gut microbial dysbiosis in individuals with Sjögren’s syndrome |
title_fullStr | Gut microbial dysbiosis in individuals with Sjögren’s syndrome |
title_full_unstemmed | Gut microbial dysbiosis in individuals with Sjögren’s syndrome |
title_short | Gut microbial dysbiosis in individuals with Sjögren’s syndrome |
title_sort | gut microbial dysbiosis in individuals with sjögren’s syndrome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7158097/ https://www.ncbi.nlm.nih.gov/pubmed/32293464 http://dx.doi.org/10.1186/s12934-020-01348-7 |
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