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Bacterial distribution on the ocular surface of patients with primary Sjögren’s syndrome

Many studies have shown that gut microbial dysbiosis is a major factor in the etiology of autoimmune diseases but none have suggested that the ocular surface (OS) microbiome is associated with Sjögren’s syndrome (SS). In this prospective study, we analyzed bacterial distribution on the OS in patient...

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Autores principales: Kim, Yong Chan, Ham, Baknoon, Kang, Kui Dong, Yun, Jun Myeong, Kwon, Man Jae, Kim, Hyun Seung, Hwang, Hyung Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8810764/
https://www.ncbi.nlm.nih.gov/pubmed/35110614
http://dx.doi.org/10.1038/s41598-022-05625-w
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author Kim, Yong Chan
Ham, Baknoon
Kang, Kui Dong
Yun, Jun Myeong
Kwon, Man Jae
Kim, Hyun Seung
Hwang, Hyung Bin
author_facet Kim, Yong Chan
Ham, Baknoon
Kang, Kui Dong
Yun, Jun Myeong
Kwon, Man Jae
Kim, Hyun Seung
Hwang, Hyung Bin
author_sort Kim, Yong Chan
collection PubMed
description Many studies have shown that gut microbial dysbiosis is a major factor in the etiology of autoimmune diseases but none have suggested that the ocular surface (OS) microbiome is associated with Sjögren’s syndrome (SS). In this prospective study, we analyzed bacterial distribution on the OS in patients with primary SS. Among the 120 subjects included in this study, 48 patients (group A) had primary SS, whereas 72 subjects (group B) had dry eye symptoms that were unrelated to SS. We evaluated clinical dry eye parameters such as the OS disease index, ocular staining score (OSS), Schirmer’s I test, and tear break-up time (TBUT). Conjunctival swabs were used to analyze the microbial communities from the two groups. Bacterial 16S rRNA genes were sequenced using the Illumina MiSeq platform, and the data were analyzed using the QIIME 1.9.1 program. The Shannon index was significantly lower in group A than in group B microbiota (p < 0.05). An analysis of similarity using the Bray–Curtis distance method found no difference in beta-diversity between the two groups (p > 0.05). In group A, Actinobacteria at the phylum level and Corynebacteria at the genus level exhibited low abundance than group B, but the differences were not statistically significant (p > 0.05). SS apparently decreases the diversity of the OS microbial community. These observations may be related to the pathophysiology of SS and should be investigated in future studies.
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spelling pubmed-88107642022-02-03 Bacterial distribution on the ocular surface of patients with primary Sjögren’s syndrome Kim, Yong Chan Ham, Baknoon Kang, Kui Dong Yun, Jun Myeong Kwon, Man Jae Kim, Hyun Seung Hwang, Hyung Bin Sci Rep Article Many studies have shown that gut microbial dysbiosis is a major factor in the etiology of autoimmune diseases but none have suggested that the ocular surface (OS) microbiome is associated with Sjögren’s syndrome (SS). In this prospective study, we analyzed bacterial distribution on the OS in patients with primary SS. Among the 120 subjects included in this study, 48 patients (group A) had primary SS, whereas 72 subjects (group B) had dry eye symptoms that were unrelated to SS. We evaluated clinical dry eye parameters such as the OS disease index, ocular staining score (OSS), Schirmer’s I test, and tear break-up time (TBUT). Conjunctival swabs were used to analyze the microbial communities from the two groups. Bacterial 16S rRNA genes were sequenced using the Illumina MiSeq platform, and the data were analyzed using the QIIME 1.9.1 program. The Shannon index was significantly lower in group A than in group B microbiota (p < 0.05). An analysis of similarity using the Bray–Curtis distance method found no difference in beta-diversity between the two groups (p > 0.05). In group A, Actinobacteria at the phylum level and Corynebacteria at the genus level exhibited low abundance than group B, but the differences were not statistically significant (p > 0.05). SS apparently decreases the diversity of the OS microbial community. These observations may be related to the pathophysiology of SS and should be investigated in future studies. Nature Publishing Group UK 2022-02-02 /pmc/articles/PMC8810764/ /pubmed/35110614 http://dx.doi.org/10.1038/s41598-022-05625-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kim, Yong Chan
Ham, Baknoon
Kang, Kui Dong
Yun, Jun Myeong
Kwon, Man Jae
Kim, Hyun Seung
Hwang, Hyung Bin
Bacterial distribution on the ocular surface of patients with primary Sjögren’s syndrome
title Bacterial distribution on the ocular surface of patients with primary Sjögren’s syndrome
title_full Bacterial distribution on the ocular surface of patients with primary Sjögren’s syndrome
title_fullStr Bacterial distribution on the ocular surface of patients with primary Sjögren’s syndrome
title_full_unstemmed Bacterial distribution on the ocular surface of patients with primary Sjögren’s syndrome
title_short Bacterial distribution on the ocular surface of patients with primary Sjögren’s syndrome
title_sort bacterial distribution on the ocular surface of patients with primary sjögren’s syndrome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8810764/
https://www.ncbi.nlm.nih.gov/pubmed/35110614
http://dx.doi.org/10.1038/s41598-022-05625-w
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