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16S rDNA analysis of periodontal plaque in chronic obstructive pulmonary disease and periodontitis patients

This study investigated if chronic obstructive pulmonary disease (COPD) is correlated with periodontitis via periodontal microbiota and if certain bacteria affect periodontitis as well as COPD. Moreover, the study investigated whether suffering from COPD is associated with a decrease in the richness...

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Autores principales: Wu, Xingwen, Chen, Jiazhen, Xu, Meng, Zhu, Danting, Wang, Xuyang, Chen, Yulin, Wu, Jing, Cui, Chenghao, Zhang, Wenhong, Yu, Liying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508401/
https://www.ncbi.nlm.nih.gov/pubmed/28748030
http://dx.doi.org/10.1080/20002297.2017.1324725
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author Wu, Xingwen
Chen, Jiazhen
Xu, Meng
Zhu, Danting
Wang, Xuyang
Chen, Yulin
Wu, Jing
Cui, Chenghao
Zhang, Wenhong
Yu, Liying
author_facet Wu, Xingwen
Chen, Jiazhen
Xu, Meng
Zhu, Danting
Wang, Xuyang
Chen, Yulin
Wu, Jing
Cui, Chenghao
Zhang, Wenhong
Yu, Liying
author_sort Wu, Xingwen
collection PubMed
description This study investigated if chronic obstructive pulmonary disease (COPD) is correlated with periodontitis via periodontal microbiota and if certain bacteria affect periodontitis as well as COPD. Moreover, the study investigated whether suffering from COPD is associated with a decrease in the richness and diversity of periodontal microbiota. Subgingival plaque was obtained from 105 patients. Bacterial DNA was isolated from 55 COPD and 50 non-COPD participants (either with or without periodontitis). 16S rRNA gene metagenomic sequencing was used to characterize the microbiota and to determine taxonomic classification. In the non-periodontitis patients, suffering from COPD resulted in a decrease in bacteria richness and diversity in the periodontal microenvironment. An increase in the genera Dysgonomonas, Desulfobulbus, and Catonella and in four species (Porphyromonas endodontalis, Dysgonomonas wimpennyi, Catonella morbi, and Prevotella intermedia) in both COPD and periodontitis patients suggests that an increase in these periodontitis-associated microbiota may be related to COPD. Three genera (Johnsonella, Campylobacter, and Oribacterium) were associated with COPD but not with periodontitis. The decrease in the genera Arcanobacterium, Oribacterium, and Streptomyces in COPD patients implies that these genera may be health-associated genera, and the decrease in these genera may be related to disease. These data support the hypothesis that COPD is correlated with periodontitis via these significantly changed specific bacteria.
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spelling pubmed-55084012017-07-26 16S rDNA analysis of periodontal plaque in chronic obstructive pulmonary disease and periodontitis patients Wu, Xingwen Chen, Jiazhen Xu, Meng Zhu, Danting Wang, Xuyang Chen, Yulin Wu, Jing Cui, Chenghao Zhang, Wenhong Yu, Liying J Oral Microbiol Perspective This study investigated if chronic obstructive pulmonary disease (COPD) is correlated with periodontitis via periodontal microbiota and if certain bacteria affect periodontitis as well as COPD. Moreover, the study investigated whether suffering from COPD is associated with a decrease in the richness and diversity of periodontal microbiota. Subgingival plaque was obtained from 105 patients. Bacterial DNA was isolated from 55 COPD and 50 non-COPD participants (either with or without periodontitis). 16S rRNA gene metagenomic sequencing was used to characterize the microbiota and to determine taxonomic classification. In the non-periodontitis patients, suffering from COPD resulted in a decrease in bacteria richness and diversity in the periodontal microenvironment. An increase in the genera Dysgonomonas, Desulfobulbus, and Catonella and in four species (Porphyromonas endodontalis, Dysgonomonas wimpennyi, Catonella morbi, and Prevotella intermedia) in both COPD and periodontitis patients suggests that an increase in these periodontitis-associated microbiota may be related to COPD. Three genera (Johnsonella, Campylobacter, and Oribacterium) were associated with COPD but not with periodontitis. The decrease in the genera Arcanobacterium, Oribacterium, and Streptomyces in COPD patients implies that these genera may be health-associated genera, and the decrease in these genera may be related to disease. These data support the hypothesis that COPD is correlated with periodontitis via these significantly changed specific bacteria. Taylor & Francis 2017-06-12 /pmc/articles/PMC5508401/ /pubmed/28748030 http://dx.doi.org/10.1080/20002297.2017.1324725 Text en © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ 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 cited.
spellingShingle Perspective
Wu, Xingwen
Chen, Jiazhen
Xu, Meng
Zhu, Danting
Wang, Xuyang
Chen, Yulin
Wu, Jing
Cui, Chenghao
Zhang, Wenhong
Yu, Liying
16S rDNA analysis of periodontal plaque in chronic obstructive pulmonary disease and periodontitis patients
title 16S rDNA analysis of periodontal plaque in chronic obstructive pulmonary disease and periodontitis patients
title_full 16S rDNA analysis of periodontal plaque in chronic obstructive pulmonary disease and periodontitis patients
title_fullStr 16S rDNA analysis of periodontal plaque in chronic obstructive pulmonary disease and periodontitis patients
title_full_unstemmed 16S rDNA analysis of periodontal plaque in chronic obstructive pulmonary disease and periodontitis patients
title_short 16S rDNA analysis of periodontal plaque in chronic obstructive pulmonary disease and periodontitis patients
title_sort 16s rdna analysis of periodontal plaque in chronic obstructive pulmonary disease and periodontitis patients
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508401/
https://www.ncbi.nlm.nih.gov/pubmed/28748030
http://dx.doi.org/10.1080/20002297.2017.1324725
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