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Oral microbiota in autoimmune polyendocrine syndrome type 1

Background: Autoimmune polyendocrine syndrome type-1 (APS-1) is a rare, childhood onset disease caused by mutations in the Autoimmune Regulator gene. The phenotypic expression is highly variable and includes disease manifestations in the oral cavity, including mucocutaneous candidiasis. Increasing e...

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Autores principales: Bruserud, Øyvind, Siddiqui, Huma, Marthinussen, Mihaela Cuida, Chen, Tsute, Jonsson, Roland, Oftedal, Bergithe Eikeland, Olsen, Ingar, Husebye, Eystein Sverre, Wolff, Anette Bøe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5827717/
https://www.ncbi.nlm.nih.gov/pubmed/29503707
http://dx.doi.org/10.1080/20002297.2018.1442986
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author Bruserud, Øyvind
Siddiqui, Huma
Marthinussen, Mihaela Cuida
Chen, Tsute
Jonsson, Roland
Oftedal, Bergithe Eikeland
Olsen, Ingar
Husebye, Eystein Sverre
Wolff, Anette Bøe
author_facet Bruserud, Øyvind
Siddiqui, Huma
Marthinussen, Mihaela Cuida
Chen, Tsute
Jonsson, Roland
Oftedal, Bergithe Eikeland
Olsen, Ingar
Husebye, Eystein Sverre
Wolff, Anette Bøe
author_sort Bruserud, Øyvind
collection PubMed
description Background: Autoimmune polyendocrine syndrome type-1 (APS-1) is a rare, childhood onset disease caused by mutations in the Autoimmune Regulator gene. The phenotypic expression is highly variable and includes disease manifestations in the oral cavity, including mucocutaneous candidiasis. Increasing evidence suggests a potential role of the skin, oral and gut microbiotas in the pathogenesis of autoimmunity. To date, no information exists regarding the oral microbiota in APS-1. Objective: To assess the bacterial microbiota of whole saliva in APS-1 patients by using high throughput sequencing. Design: Whole unstimulated saliva was collected from 10 APS-1 patients and 17 healthy controls and examined by high throughput sequencing of the hypervariable region V1-V2 of 16S rRNA using the 454 GS Junior system. Metastats (http://cbcb.umd.edu/software/metastats) was used to analyse the pyrosequencing reads. Results: A reduction in the total number of bacterial genera and species was detected in APS-1 compared to healthy controls. The proportion of the major phyla Firmicutes was higher (60% vs 41%, p = 0.002) and Bacteroidetes lower (15% vs 28%, p = 0.007) in APS-1 compared to healthy controls. On the genus level, Streptococcus and Gemella were prevalent in APS-1. Conclusion: Our findings indicate a significantly altered oral microbiota in APS-1.
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spelling pubmed-58277172018-03-02 Oral microbiota in autoimmune polyendocrine syndrome type 1 Bruserud, Øyvind Siddiqui, Huma Marthinussen, Mihaela Cuida Chen, Tsute Jonsson, Roland Oftedal, Bergithe Eikeland Olsen, Ingar Husebye, Eystein Sverre Wolff, Anette Bøe J Oral Microbiol Original Article Background: Autoimmune polyendocrine syndrome type-1 (APS-1) is a rare, childhood onset disease caused by mutations in the Autoimmune Regulator gene. The phenotypic expression is highly variable and includes disease manifestations in the oral cavity, including mucocutaneous candidiasis. Increasing evidence suggests a potential role of the skin, oral and gut microbiotas in the pathogenesis of autoimmunity. To date, no information exists regarding the oral microbiota in APS-1. Objective: To assess the bacterial microbiota of whole saliva in APS-1 patients by using high throughput sequencing. Design: Whole unstimulated saliva was collected from 10 APS-1 patients and 17 healthy controls and examined by high throughput sequencing of the hypervariable region V1-V2 of 16S rRNA using the 454 GS Junior system. Metastats (http://cbcb.umd.edu/software/metastats) was used to analyse the pyrosequencing reads. Results: A reduction in the total number of bacterial genera and species was detected in APS-1 compared to healthy controls. The proportion of the major phyla Firmicutes was higher (60% vs 41%, p = 0.002) and Bacteroidetes lower (15% vs 28%, p = 0.007) in APS-1 compared to healthy controls. On the genus level, Streptococcus and Gemella were prevalent in APS-1. Conclusion: Our findings indicate a significantly altered oral microbiota in APS-1. Taylor & Francis 2018-02-26 /pmc/articles/PMC5827717/ /pubmed/29503707 http://dx.doi.org/10.1080/20002297.2018.1442986 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Bruserud, Øyvind
Siddiqui, Huma
Marthinussen, Mihaela Cuida
Chen, Tsute
Jonsson, Roland
Oftedal, Bergithe Eikeland
Olsen, Ingar
Husebye, Eystein Sverre
Wolff, Anette Bøe
Oral microbiota in autoimmune polyendocrine syndrome type 1
title Oral microbiota in autoimmune polyendocrine syndrome type 1
title_full Oral microbiota in autoimmune polyendocrine syndrome type 1
title_fullStr Oral microbiota in autoimmune polyendocrine syndrome type 1
title_full_unstemmed Oral microbiota in autoimmune polyendocrine syndrome type 1
title_short Oral microbiota in autoimmune polyendocrine syndrome type 1
title_sort oral microbiota in autoimmune polyendocrine syndrome type 1
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5827717/
https://www.ncbi.nlm.nih.gov/pubmed/29503707
http://dx.doi.org/10.1080/20002297.2018.1442986
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