Oral microbiota in autoimmune polyendocrine syndrome type 1

J Oral Microbiol. 2018 Feb 26;10(1):1442986. doi: 10.1080/20002297.2018.1442986. eCollection 2018.

Abstract

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.

Keywords: APS-1; bacteria; high throughput sequencing; microbiota; pyrosequencing; whole saliva.

Grants and funding

This study was supported by grants from the University of Bergen, the Bergen Research Foundation, Stiftelsen KG Jebsen, the Regional Health Authorities of Western Norway (grant no 977878), The Norwegian Research Council (grant no 213704) and the Novo Nordisk Foundation (grant no NNF14OC0011005). IO was funded by the European Commission (FP7-HEALTH-306029 ‘TRIGGER’). RJ was funded by EU H2020 contract HarmonicSS (contract nr: H2020-SC1-2016-RTD/731944) and the Broegelmann Foundation. Grant from Research Council of Norway (250030) to BEO