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Patients With Reflux Esophagitis Possess a Possible Different Oral Microbiota Compared With Healthy Controls

BACKGROUND AND AIM: Reflux Esophagitis (RE) is caused by a variety of factors including anatomical and functional alterations involved in the pathogenesis. Oral microbiota is influenced by many factors such as heredity, nutrition, environments and host conditions, but little is known about relations...

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Autores principales: Wang, Baoyong, Zhang, Yu, Zhao, Qiaofei, Yan, Yifan, Yang, Tian, Xia, Yanli, Chen, Hongwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7358540/
https://www.ncbi.nlm.nih.gov/pubmed/32733243
http://dx.doi.org/10.3389/fphar.2020.01000
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author Wang, Baoyong
Zhang, Yu
Zhao, Qiaofei
Yan, Yifan
Yang, Tian
Xia, Yanli
Chen, Hongwei
author_facet Wang, Baoyong
Zhang, Yu
Zhao, Qiaofei
Yan, Yifan
Yang, Tian
Xia, Yanli
Chen, Hongwei
author_sort Wang, Baoyong
collection PubMed
description BACKGROUND AND AIM: Reflux Esophagitis (RE) is caused by a variety of factors including anatomical and functional alterations involved in the pathogenesis. Oral microbiota is influenced by many factors such as heredity, nutrition, environments and host conditions, but little is known about relationship between oral microbiota and RE. The aim of this study was to explore whether the oral microbiota is changed in patients with RE. METHODS: To clarify this correlation, fresh saliva samples from all subjects were collected and then oral microorganism diversity was analysed in 55 patients with RE and 51 controls via hypervariable tag sequencing and analyzing the V3–V4 region of the 16S rDNA gene. RESULTS: There was no difference found in oral microbial diversity between RE patients and healthy controls by Shannon diversity index (p=0.60) and Simpson diversity index (p= 0.38). The abundance of Proteobacteria was lower, but Bacteroidetes was higher in patients with RE at the phylum level. At the genus level the abundances of Prevotella, Veillonella, Megasphaera, Peptostreptococcus, Atopobium, Oribacterium, Eubacterium, and Lachnoanaerobaculum were increased, while Neisseria, Streptococcus, Rothia, Granulicatella, Gemella, Aggregatibacter, Treponema, Campylobacter, Filifactor, Corynebacterium, and Lactivibrio were decreased in RE patients than the controls. CONCLUSIONS: Our study suggested oral microbial dysbiosis in patients with RE, and identified bacterial species with potential biomarker significance. Further studies are required to understand role of oral microbial dysbiosis in the pathogenesis of RE.
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spelling pubmed-73585402020-07-29 Patients With Reflux Esophagitis Possess a Possible Different Oral Microbiota Compared With Healthy Controls Wang, Baoyong Zhang, Yu Zhao, Qiaofei Yan, Yifan Yang, Tian Xia, Yanli Chen, Hongwei Front Pharmacol Pharmacology BACKGROUND AND AIM: Reflux Esophagitis (RE) is caused by a variety of factors including anatomical and functional alterations involved in the pathogenesis. Oral microbiota is influenced by many factors such as heredity, nutrition, environments and host conditions, but little is known about relationship between oral microbiota and RE. The aim of this study was to explore whether the oral microbiota is changed in patients with RE. METHODS: To clarify this correlation, fresh saliva samples from all subjects were collected and then oral microorganism diversity was analysed in 55 patients with RE and 51 controls via hypervariable tag sequencing and analyzing the V3–V4 region of the 16S rDNA gene. RESULTS: There was no difference found in oral microbial diversity between RE patients and healthy controls by Shannon diversity index (p=0.60) and Simpson diversity index (p= 0.38). The abundance of Proteobacteria was lower, but Bacteroidetes was higher in patients with RE at the phylum level. At the genus level the abundances of Prevotella, Veillonella, Megasphaera, Peptostreptococcus, Atopobium, Oribacterium, Eubacterium, and Lachnoanaerobaculum were increased, while Neisseria, Streptococcus, Rothia, Granulicatella, Gemella, Aggregatibacter, Treponema, Campylobacter, Filifactor, Corynebacterium, and Lactivibrio were decreased in RE patients than the controls. CONCLUSIONS: Our study suggested oral microbial dysbiosis in patients with RE, and identified bacterial species with potential biomarker significance. Further studies are required to understand role of oral microbial dysbiosis in the pathogenesis of RE. Frontiers Media S.A. 2020-07-07 /pmc/articles/PMC7358540/ /pubmed/32733243 http://dx.doi.org/10.3389/fphar.2020.01000 Text en Copyright © 2020 Wang, Zhang, Zhao, Yan, Yang, Xia and Chen http://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 Pharmacology
Wang, Baoyong
Zhang, Yu
Zhao, Qiaofei
Yan, Yifan
Yang, Tian
Xia, Yanli
Chen, Hongwei
Patients With Reflux Esophagitis Possess a Possible Different Oral Microbiota Compared With Healthy Controls
title Patients With Reflux Esophagitis Possess a Possible Different Oral Microbiota Compared With Healthy Controls
title_full Patients With Reflux Esophagitis Possess a Possible Different Oral Microbiota Compared With Healthy Controls
title_fullStr Patients With Reflux Esophagitis Possess a Possible Different Oral Microbiota Compared With Healthy Controls
title_full_unstemmed Patients With Reflux Esophagitis Possess a Possible Different Oral Microbiota Compared With Healthy Controls
title_short Patients With Reflux Esophagitis Possess a Possible Different Oral Microbiota Compared With Healthy Controls
title_sort patients with reflux esophagitis possess a possible different oral microbiota compared with healthy controls
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7358540/
https://www.ncbi.nlm.nih.gov/pubmed/32733243
http://dx.doi.org/10.3389/fphar.2020.01000
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