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Inflammation-associated microbiota in pediatric eosinophilic esophagitis

BACKGROUND: Eosinophilic esophagitis (EoE) is an allergic disorder characterized by eosinophil-predominant esophageal inflammation, which can be ameliorated by food antigen restriction. Though recent studies suggest that changes in dietary composition may alter the distal gut microbiome, little is c...

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Autores principales: Benitez, Alain J, Hoffmann, Christian, Muir, Amanda B., Dods, Kara K., Spergel, Jonathan M., Bushman, Frederic D., Wang, Mei-Lun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4450515/
https://www.ncbi.nlm.nih.gov/pubmed/26034601
http://dx.doi.org/10.1186/s40168-015-0085-6
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author Benitez, Alain J
Hoffmann, Christian
Muir, Amanda B.
Dods, Kara K.
Spergel, Jonathan M.
Bushman, Frederic D.
Wang, Mei-Lun
author_facet Benitez, Alain J
Hoffmann, Christian
Muir, Amanda B.
Dods, Kara K.
Spergel, Jonathan M.
Bushman, Frederic D.
Wang, Mei-Lun
author_sort Benitez, Alain J
collection PubMed
description BACKGROUND: Eosinophilic esophagitis (EoE) is an allergic disorder characterized by eosinophil-predominant esophageal inflammation, which can be ameliorated by food antigen restriction. Though recent studies suggest that changes in dietary composition may alter the distal gut microbiome, little is currently known about the impact of a restricted diet upon microbial communities of the oral and esophageal microenvironments in the context of EoE. We hypothesize that the oral and esophageal microbiomes of EoE patients are distinct from non-EoE controls, that these differences correspond to changes in esophageal inflammation, and that targeted therapeutic dietary intervention may influence community structure. Using 16S rRNA gene sequencing, we characterized the bacterial composition of the oral and esophageal microenvironments using oral swabs and esophageal biopsies from 35 non-EoE pediatric controls and compared this cohort to samples from 33 pediatric EoE subjects studied in a longitudinal fashion before and after defined dietary changes. RESULTS: Firmicutes were more abundant in esophageal samples compared to oral. Proportions of bacterial communities were significantly different comparing all EoE esophageal microbiota to non-EoE controls, with enrichment of Proteobacteria, including Neisseria and Corynebacterium in the EoE cohort, and predominance of the Firmicutes in non-EoE control subjects. We detected a statistically significant difference between actively inflamed EoE biopsies and non-EoE controls. Overall, though targeted dietary intervention did not lead to significant differences in either oral or esophageal microbiota, reintroduction of highly allergenic foods led to enrichment in Ganulicatella and Campylobacter genera in the esophagus. CONCLUSIONS: In conclusion, the esophageal microbiome in EoE is distinct from that of non-EoE controls, with maximal differences observed during active allergic inflammation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40168-015-0085-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-44505152015-06-02 Inflammation-associated microbiota in pediatric eosinophilic esophagitis Benitez, Alain J Hoffmann, Christian Muir, Amanda B. Dods, Kara K. Spergel, Jonathan M. Bushman, Frederic D. Wang, Mei-Lun Microbiome Research BACKGROUND: Eosinophilic esophagitis (EoE) is an allergic disorder characterized by eosinophil-predominant esophageal inflammation, which can be ameliorated by food antigen restriction. Though recent studies suggest that changes in dietary composition may alter the distal gut microbiome, little is currently known about the impact of a restricted diet upon microbial communities of the oral and esophageal microenvironments in the context of EoE. We hypothesize that the oral and esophageal microbiomes of EoE patients are distinct from non-EoE controls, that these differences correspond to changes in esophageal inflammation, and that targeted therapeutic dietary intervention may influence community structure. Using 16S rRNA gene sequencing, we characterized the bacterial composition of the oral and esophageal microenvironments using oral swabs and esophageal biopsies from 35 non-EoE pediatric controls and compared this cohort to samples from 33 pediatric EoE subjects studied in a longitudinal fashion before and after defined dietary changes. RESULTS: Firmicutes were more abundant in esophageal samples compared to oral. Proportions of bacterial communities were significantly different comparing all EoE esophageal microbiota to non-EoE controls, with enrichment of Proteobacteria, including Neisseria and Corynebacterium in the EoE cohort, and predominance of the Firmicutes in non-EoE control subjects. We detected a statistically significant difference between actively inflamed EoE biopsies and non-EoE controls. Overall, though targeted dietary intervention did not lead to significant differences in either oral or esophageal microbiota, reintroduction of highly allergenic foods led to enrichment in Ganulicatella and Campylobacter genera in the esophagus. CONCLUSIONS: In conclusion, the esophageal microbiome in EoE is distinct from that of non-EoE controls, with maximal differences observed during active allergic inflammation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40168-015-0085-6) contains supplementary material, which is available to authorized users. BioMed Central 2015-06-01 /pmc/articles/PMC4450515/ /pubmed/26034601 http://dx.doi.org/10.1186/s40168-015-0085-6 Text en © Benitez et al.; licensee BioMed Central. 2015 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 credited. 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
Benitez, Alain J
Hoffmann, Christian
Muir, Amanda B.
Dods, Kara K.
Spergel, Jonathan M.
Bushman, Frederic D.
Wang, Mei-Lun
Inflammation-associated microbiota in pediatric eosinophilic esophagitis
title Inflammation-associated microbiota in pediatric eosinophilic esophagitis
title_full Inflammation-associated microbiota in pediatric eosinophilic esophagitis
title_fullStr Inflammation-associated microbiota in pediatric eosinophilic esophagitis
title_full_unstemmed Inflammation-associated microbiota in pediatric eosinophilic esophagitis
title_short Inflammation-associated microbiota in pediatric eosinophilic esophagitis
title_sort inflammation-associated microbiota in pediatric eosinophilic esophagitis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4450515/
https://www.ncbi.nlm.nih.gov/pubmed/26034601
http://dx.doi.org/10.1186/s40168-015-0085-6
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