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Mucosal and salivary microbiota associated with recurrent aphthous stomatitis
BACKGROUND: Recurrent aphthous stomatitis (RAS) is a common oral mucosal disorder of unclear etiopathogenesis. Although recent studies of the oral microbiota by high-throughput sequencing of 16S rRNA genes have suggested that imbalances in the oral microbiota may contribute to the etiopathogenesis o...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818471/ https://www.ncbi.nlm.nih.gov/pubmed/27036492 http://dx.doi.org/10.1186/s12866-016-0673-z |
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author | Kim, Yun-ji Choi, Yun Sik Baek, Keum Jin Yoon, Seok-Hwan Park, Hee Kyung Choi, Youngnim |
author_facet | Kim, Yun-ji Choi, Yun Sik Baek, Keum Jin Yoon, Seok-Hwan Park, Hee Kyung Choi, Youngnim |
author_sort | Kim, Yun-ji |
collection | PubMed |
description | BACKGROUND: Recurrent aphthous stomatitis (RAS) is a common oral mucosal disorder of unclear etiopathogenesis. Although recent studies of the oral microbiota by high-throughput sequencing of 16S rRNA genes have suggested that imbalances in the oral microbiota may contribute to the etiopathogenesis of RAS, no specific bacterial species associated with RAS have been identified. The present study aimed to characterize the microbiota in the oral mucosa and saliva of RAS patients in comparison with control subjects at the species level. RESULTS: The bacterial communities of the oral mucosa and saliva from RAS patients with active lesions (RAS, n = 18 for mucosa and n = 8 for saliva) and control subjects (n = 18 for mucosa and n = 7 for saliva) were analyzed by pyrosequencing of the 16S rRNA genes. There were no significant differences in the alpha diversity between the controls and the RAS, but the mucosal microbiota of the RAS patients showed increased inter-subject variability. A comparison of the relative abundance of each taxon revealed decreases in the members of healthy core microbiota but increases of rare species in the mucosal and salivary microbiota of RAS patients. Particularly, decreased Streptococcus salivarius and increased Acinetobacter johnsonii in the mucosa were associated with RAS risk. A dysbiosis index, which was developed using the relative abundance of A. johnsonii and S. salivarius and the regression coefficients, correctly predicted 83 % of the total cases for the absence or presence of RAS. Interestingly, A. johnsonii substantially inhibited the proliferation of gingival epithelial cells and showed greater cytotoxicity against the gingival epithelial cells than S. salivarius. CONCLUSION: RAS is associated with dysbiosis of the mucosal and salivary microbiota, and two species associated with RAS have been identified. This knowledge may provide a diagnostic tool and new targets for therapeutics for RAS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12866-016-0673-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4818471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48184712016-04-03 Mucosal and salivary microbiota associated with recurrent aphthous stomatitis Kim, Yun-ji Choi, Yun Sik Baek, Keum Jin Yoon, Seok-Hwan Park, Hee Kyung Choi, Youngnim BMC Microbiol Research Article BACKGROUND: Recurrent aphthous stomatitis (RAS) is a common oral mucosal disorder of unclear etiopathogenesis. Although recent studies of the oral microbiota by high-throughput sequencing of 16S rRNA genes have suggested that imbalances in the oral microbiota may contribute to the etiopathogenesis of RAS, no specific bacterial species associated with RAS have been identified. The present study aimed to characterize the microbiota in the oral mucosa and saliva of RAS patients in comparison with control subjects at the species level. RESULTS: The bacterial communities of the oral mucosa and saliva from RAS patients with active lesions (RAS, n = 18 for mucosa and n = 8 for saliva) and control subjects (n = 18 for mucosa and n = 7 for saliva) were analyzed by pyrosequencing of the 16S rRNA genes. There were no significant differences in the alpha diversity between the controls and the RAS, but the mucosal microbiota of the RAS patients showed increased inter-subject variability. A comparison of the relative abundance of each taxon revealed decreases in the members of healthy core microbiota but increases of rare species in the mucosal and salivary microbiota of RAS patients. Particularly, decreased Streptococcus salivarius and increased Acinetobacter johnsonii in the mucosa were associated with RAS risk. A dysbiosis index, which was developed using the relative abundance of A. johnsonii and S. salivarius and the regression coefficients, correctly predicted 83 % of the total cases for the absence or presence of RAS. Interestingly, A. johnsonii substantially inhibited the proliferation of gingival epithelial cells and showed greater cytotoxicity against the gingival epithelial cells than S. salivarius. CONCLUSION: RAS is associated with dysbiosis of the mucosal and salivary microbiota, and two species associated with RAS have been identified. This knowledge may provide a diagnostic tool and new targets for therapeutics for RAS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12866-016-0673-z) contains supplementary material, which is available to authorized users. BioMed Central 2016-04-01 /pmc/articles/PMC4818471/ /pubmed/27036492 http://dx.doi.org/10.1186/s12866-016-0673-z Text en © Kim et al. 2016 Open AccessThis 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. 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. |
spellingShingle | Research Article Kim, Yun-ji Choi, Yun Sik Baek, Keum Jin Yoon, Seok-Hwan Park, Hee Kyung Choi, Youngnim Mucosal and salivary microbiota associated with recurrent aphthous stomatitis |
title | Mucosal and salivary microbiota associated with recurrent aphthous stomatitis |
title_full | Mucosal and salivary microbiota associated with recurrent aphthous stomatitis |
title_fullStr | Mucosal and salivary microbiota associated with recurrent aphthous stomatitis |
title_full_unstemmed | Mucosal and salivary microbiota associated with recurrent aphthous stomatitis |
title_short | Mucosal and salivary microbiota associated with recurrent aphthous stomatitis |
title_sort | mucosal and salivary microbiota associated with recurrent aphthous stomatitis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818471/ https://www.ncbi.nlm.nih.gov/pubmed/27036492 http://dx.doi.org/10.1186/s12866-016-0673-z |
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