Cargando…

Fecal Bacteria Implicated in Biofilm Production Are Enriched and Associate to Gastrointestinal Symptoms in Patients With APECED – A Pilot Study

BACKGROUNDS AND AIMS: APECED is a rare autoimmune disease caused by mutations in the Autoimmune Regulator gene. A significant proportion of patients also have gastrointestinal symptoms, including malabsorption, chronic diarrhea, and obstipation. The pathological background of the gastrointestinal sy...

Descripción completa

Detalles Bibliográficos
Autores principales: Hetemäki, Iivo, Jian, Ching, Laakso, Saila, Mäkitie, Outi, Pajari, Anne-Maria, de Vos, Willem M., Arstila, T. Petteri, Salonen, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8339580/
https://www.ncbi.nlm.nih.gov/pubmed/34367134
http://dx.doi.org/10.3389/fimmu.2021.668219
_version_ 1783733631588499456
author Hetemäki, Iivo
Jian, Ching
Laakso, Saila
Mäkitie, Outi
Pajari, Anne-Maria
de Vos, Willem M.
Arstila, T. Petteri
Salonen, Anne
author_facet Hetemäki, Iivo
Jian, Ching
Laakso, Saila
Mäkitie, Outi
Pajari, Anne-Maria
de Vos, Willem M.
Arstila, T. Petteri
Salonen, Anne
author_sort Hetemäki, Iivo
collection PubMed
description BACKGROUNDS AND AIMS: APECED is a rare autoimmune disease caused by mutations in the Autoimmune Regulator gene. A significant proportion of patients also have gastrointestinal symptoms, including malabsorption, chronic diarrhea, and obstipation. The pathological background of the gastrointestinal symptoms remains incompletely understood and involves multiple factors, with autoimmunity being the most common underlying cause. Patients with APECED have increased immune responses against gut commensals. Our objective was to evaluate whether the intestinal microbiota composition, predicted functions or fungal abundance differ between Finnish patients with APECED and healthy controls, and whether these associate to the patients’ clinical phenotype and gastrointestinal symptoms. METHODS: DNA was isolated from fecal samples from 15 patients with APECED (median age 46.4 years) together with 15 samples from body mass index matched healthy controls. DNA samples were subjected to analysis of the gut microbiota using 16S rRNA gene amplicon sequencing, imputed metagenomics using the PICRUSt2 algorithm, and quantitative PCR for fungi. Extensive correlations of the microbiota with patient characteristics were determined. RESULTS: Analysis of gut microbiota indicated that both alpha- and beta-diversity were altered in patients with APECED compared to healthy controls. The fraction of Faecalibacterium was reduced in patients with APECED while that of Atopobium spp. and several gram-negative genera previously implicated in biofilm formation, e.g. Veillonella, Prevotella, Megasphaera and Heamophilus, were increased in parallel to lipopolysaccharide (LPS) synthesis in imputed metagenomics. The differences in gut microbiota were linked to patient characteristics, especially the presence of anti-Saccharomyces cerevisiae antibodies (ASCA) and severity of gastrointestinal symptoms. CONCLUSIONS: Gut microbiota of patients with APECED is altered and enriched with predominantly gram-negative bacterial taxa that may promote biofilm formation and lead to increased exposure to LPS in the patients. The most pronounced alterations in the microbiota were associated with more severe gastrointestinal symptoms.
format Online
Article
Text
id pubmed-8339580
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-83395802021-08-06 Fecal Bacteria Implicated in Biofilm Production Are Enriched and Associate to Gastrointestinal Symptoms in Patients With APECED – A Pilot Study Hetemäki, Iivo Jian, Ching Laakso, Saila Mäkitie, Outi Pajari, Anne-Maria de Vos, Willem M. Arstila, T. Petteri Salonen, Anne Front Immunol Immunology BACKGROUNDS AND AIMS: APECED is a rare autoimmune disease caused by mutations in the Autoimmune Regulator gene. A significant proportion of patients also have gastrointestinal symptoms, including malabsorption, chronic diarrhea, and obstipation. The pathological background of the gastrointestinal symptoms remains incompletely understood and involves multiple factors, with autoimmunity being the most common underlying cause. Patients with APECED have increased immune responses against gut commensals. Our objective was to evaluate whether the intestinal microbiota composition, predicted functions or fungal abundance differ between Finnish patients with APECED and healthy controls, and whether these associate to the patients’ clinical phenotype and gastrointestinal symptoms. METHODS: DNA was isolated from fecal samples from 15 patients with APECED (median age 46.4 years) together with 15 samples from body mass index matched healthy controls. DNA samples were subjected to analysis of the gut microbiota using 16S rRNA gene amplicon sequencing, imputed metagenomics using the PICRUSt2 algorithm, and quantitative PCR for fungi. Extensive correlations of the microbiota with patient characteristics were determined. RESULTS: Analysis of gut microbiota indicated that both alpha- and beta-diversity were altered in patients with APECED compared to healthy controls. The fraction of Faecalibacterium was reduced in patients with APECED while that of Atopobium spp. and several gram-negative genera previously implicated in biofilm formation, e.g. Veillonella, Prevotella, Megasphaera and Heamophilus, were increased in parallel to lipopolysaccharide (LPS) synthesis in imputed metagenomics. The differences in gut microbiota were linked to patient characteristics, especially the presence of anti-Saccharomyces cerevisiae antibodies (ASCA) and severity of gastrointestinal symptoms. CONCLUSIONS: Gut microbiota of patients with APECED is altered and enriched with predominantly gram-negative bacterial taxa that may promote biofilm formation and lead to increased exposure to LPS in the patients. The most pronounced alterations in the microbiota were associated with more severe gastrointestinal symptoms. Frontiers Media S.A. 2021-07-22 /pmc/articles/PMC8339580/ /pubmed/34367134 http://dx.doi.org/10.3389/fimmu.2021.668219 Text en Copyright © 2021 Hetemäki, Jian, Laakso, Mäkitie, Pajari, de Vos, Arstila and Salonen https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Hetemäki, Iivo
Jian, Ching
Laakso, Saila
Mäkitie, Outi
Pajari, Anne-Maria
de Vos, Willem M.
Arstila, T. Petteri
Salonen, Anne
Fecal Bacteria Implicated in Biofilm Production Are Enriched and Associate to Gastrointestinal Symptoms in Patients With APECED – A Pilot Study
title Fecal Bacteria Implicated in Biofilm Production Are Enriched and Associate to Gastrointestinal Symptoms in Patients With APECED – A Pilot Study
title_full Fecal Bacteria Implicated in Biofilm Production Are Enriched and Associate to Gastrointestinal Symptoms in Patients With APECED – A Pilot Study
title_fullStr Fecal Bacteria Implicated in Biofilm Production Are Enriched and Associate to Gastrointestinal Symptoms in Patients With APECED – A Pilot Study
title_full_unstemmed Fecal Bacteria Implicated in Biofilm Production Are Enriched and Associate to Gastrointestinal Symptoms in Patients With APECED – A Pilot Study
title_short Fecal Bacteria Implicated in Biofilm Production Are Enriched and Associate to Gastrointestinal Symptoms in Patients With APECED – A Pilot Study
title_sort fecal bacteria implicated in biofilm production are enriched and associate to gastrointestinal symptoms in patients with apeced – a pilot study
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8339580/
https://www.ncbi.nlm.nih.gov/pubmed/34367134
http://dx.doi.org/10.3389/fimmu.2021.668219
work_keys_str_mv AT hetemakiiivo fecalbacteriaimplicatedinbiofilmproductionareenrichedandassociatetogastrointestinalsymptomsinpatientswithapecedapilotstudy
AT jianching fecalbacteriaimplicatedinbiofilmproductionareenrichedandassociatetogastrointestinalsymptomsinpatientswithapecedapilotstudy
AT laaksosaila fecalbacteriaimplicatedinbiofilmproductionareenrichedandassociatetogastrointestinalsymptomsinpatientswithapecedapilotstudy
AT makitieouti fecalbacteriaimplicatedinbiofilmproductionareenrichedandassociatetogastrointestinalsymptomsinpatientswithapecedapilotstudy
AT pajariannemaria fecalbacteriaimplicatedinbiofilmproductionareenrichedandassociatetogastrointestinalsymptomsinpatientswithapecedapilotstudy
AT devoswillemm fecalbacteriaimplicatedinbiofilmproductionareenrichedandassociatetogastrointestinalsymptomsinpatientswithapecedapilotstudy
AT arstilatpetteri fecalbacteriaimplicatedinbiofilmproductionareenrichedandassociatetogastrointestinalsymptomsinpatientswithapecedapilotstudy
AT salonenanne fecalbacteriaimplicatedinbiofilmproductionareenrichedandassociatetogastrointestinalsymptomsinpatientswithapecedapilotstudy