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Oral Microbiota Profile in Patients with Anti-Neutrophil Cytoplasmic Antibody–Associated Vasculitis

Microbiota has been associated with autoimmune diseases, with nasal Staphylococcus aureus being implicated in the pathogenesis of anti-neutrophil cytoplasmic antibody–associated vasculitis (AAV). Little is known about the role of oral microbiota in AAV. In this study, levels of IgG antibodies to 53...

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Autores principales: Esberg, Anders, Johansson, Linda, Berglin, Ewa, Mohammad, Aladdin J., Jonsson, Andreas P., Dahlqvist, Johanna, Stegmayr, Bernd, Johansson, Ingegerd, Rantapää-Dahlqvist, Solbritt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9412476/
https://www.ncbi.nlm.nih.gov/pubmed/36013990
http://dx.doi.org/10.3390/microorganisms10081572
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author Esberg, Anders
Johansson, Linda
Berglin, Ewa
Mohammad, Aladdin J.
Jonsson, Andreas P.
Dahlqvist, Johanna
Stegmayr, Bernd
Johansson, Ingegerd
Rantapää-Dahlqvist, Solbritt
author_facet Esberg, Anders
Johansson, Linda
Berglin, Ewa
Mohammad, Aladdin J.
Jonsson, Andreas P.
Dahlqvist, Johanna
Stegmayr, Bernd
Johansson, Ingegerd
Rantapää-Dahlqvist, Solbritt
author_sort Esberg, Anders
collection PubMed
description Microbiota has been associated with autoimmune diseases, with nasal Staphylococcus aureus being implicated in the pathogenesis of anti-neutrophil cytoplasmic antibody–associated vasculitis (AAV). Little is known about the role of oral microbiota in AAV. In this study, levels of IgG antibodies to 53 oral bacterial species/subspecies were screened using immunoblotting in plasma/serum in pre-symptomatic AAV-individuals (n = 85), matched controls, and established AAV-patients (n = 78). Saliva microbiota from acute-AAV and controls was sequenced from 16s rDNA amplicons. Information on dental status was extracted from a national register. IgG levels against oral bacteria were lower in established AAV versus pre-AAV and controls. Specifically, pre-AAV samples had, compared to controls, a higher abundance of periodontitis-associated species paralleling more signs of periodontitis in established AAV-patients than controls. Saliva microbiota in acute-AAV showed higher within-sample diversity but fewer detectable amplicon-sequence variants and taxa in their core microbiota than controls. Acute-AAV was not associated with increased abundance of periodontal bacteria but species in, e.g., Arthrospira, Staphylococcus, Lactobacillus, and Scardovia. In conclusion, the IgG profiles against oral bacteria differed between pre-AAV, established AAV, and controls, and microbiota profiles between acute AAV and controls. The IgG shift from a pre-symptomatic stage to established disease cooccurred with treatment of immunosuppression and/or antibiotics.
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spelling pubmed-94124762022-08-27 Oral Microbiota Profile in Patients with Anti-Neutrophil Cytoplasmic Antibody–Associated Vasculitis Esberg, Anders Johansson, Linda Berglin, Ewa Mohammad, Aladdin J. Jonsson, Andreas P. Dahlqvist, Johanna Stegmayr, Bernd Johansson, Ingegerd Rantapää-Dahlqvist, Solbritt Microorganisms Article Microbiota has been associated with autoimmune diseases, with nasal Staphylococcus aureus being implicated in the pathogenesis of anti-neutrophil cytoplasmic antibody–associated vasculitis (AAV). Little is known about the role of oral microbiota in AAV. In this study, levels of IgG antibodies to 53 oral bacterial species/subspecies were screened using immunoblotting in plasma/serum in pre-symptomatic AAV-individuals (n = 85), matched controls, and established AAV-patients (n = 78). Saliva microbiota from acute-AAV and controls was sequenced from 16s rDNA amplicons. Information on dental status was extracted from a national register. IgG levels against oral bacteria were lower in established AAV versus pre-AAV and controls. Specifically, pre-AAV samples had, compared to controls, a higher abundance of periodontitis-associated species paralleling more signs of periodontitis in established AAV-patients than controls. Saliva microbiota in acute-AAV showed higher within-sample diversity but fewer detectable amplicon-sequence variants and taxa in their core microbiota than controls. Acute-AAV was not associated with increased abundance of periodontal bacteria but species in, e.g., Arthrospira, Staphylococcus, Lactobacillus, and Scardovia. In conclusion, the IgG profiles against oral bacteria differed between pre-AAV, established AAV, and controls, and microbiota profiles between acute AAV and controls. The IgG shift from a pre-symptomatic stage to established disease cooccurred with treatment of immunosuppression and/or antibiotics. MDPI 2022-08-04 /pmc/articles/PMC9412476/ /pubmed/36013990 http://dx.doi.org/10.3390/microorganisms10081572 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Esberg, Anders
Johansson, Linda
Berglin, Ewa
Mohammad, Aladdin J.
Jonsson, Andreas P.
Dahlqvist, Johanna
Stegmayr, Bernd
Johansson, Ingegerd
Rantapää-Dahlqvist, Solbritt
Oral Microbiota Profile in Patients with Anti-Neutrophil Cytoplasmic Antibody–Associated Vasculitis
title Oral Microbiota Profile in Patients with Anti-Neutrophil Cytoplasmic Antibody–Associated Vasculitis
title_full Oral Microbiota Profile in Patients with Anti-Neutrophil Cytoplasmic Antibody–Associated Vasculitis
title_fullStr Oral Microbiota Profile in Patients with Anti-Neutrophil Cytoplasmic Antibody–Associated Vasculitis
title_full_unstemmed Oral Microbiota Profile in Patients with Anti-Neutrophil Cytoplasmic Antibody–Associated Vasculitis
title_short Oral Microbiota Profile in Patients with Anti-Neutrophil Cytoplasmic Antibody–Associated Vasculitis
title_sort oral microbiota profile in patients with anti-neutrophil cytoplasmic antibody–associated vasculitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9412476/
https://www.ncbi.nlm.nih.gov/pubmed/36013990
http://dx.doi.org/10.3390/microorganisms10081572
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