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Oral microbial dysbiosis in patients with periodontitis and chronic obstructive pulmonary disease

BACKGROUND: Oral microbiota is closely related to the homeostasis of the oral cavity and lungs. To provide potential information for the prediction, screening, and treatment strategies of individuals, this study compared and investigated the bacterial signatures in periodontitis and chronic obstruct...

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Autores principales: Liu, Siqin, Xie, Guofang, Chen, Meifeng, He, Yukun, Yu, Wenyi, Chen, Xiaobo, Mao, Weigang, Liu, Nanxia, Zhang, Yuanjie, Chang, Qin, Qiao, Yingying, Ma, Xinqian, Xue, Jianbo, Jin, Mengtong, Guo, Shuming, Hou, Yudong, Gao, Zhancheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9948037/
https://www.ncbi.nlm.nih.gov/pubmed/36844402
http://dx.doi.org/10.3389/fcimb.2023.1121399
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author Liu, Siqin
Xie, Guofang
Chen, Meifeng
He, Yukun
Yu, Wenyi
Chen, Xiaobo
Mao, Weigang
Liu, Nanxia
Zhang, Yuanjie
Chang, Qin
Qiao, Yingying
Ma, Xinqian
Xue, Jianbo
Jin, Mengtong
Guo, Shuming
Hou, Yudong
Gao, Zhancheng
author_facet Liu, Siqin
Xie, Guofang
Chen, Meifeng
He, Yukun
Yu, Wenyi
Chen, Xiaobo
Mao, Weigang
Liu, Nanxia
Zhang, Yuanjie
Chang, Qin
Qiao, Yingying
Ma, Xinqian
Xue, Jianbo
Jin, Mengtong
Guo, Shuming
Hou, Yudong
Gao, Zhancheng
author_sort Liu, Siqin
collection PubMed
description BACKGROUND: Oral microbiota is closely related to the homeostasis of the oral cavity and lungs. To provide potential information for the prediction, screening, and treatment strategies of individuals, this study compared and investigated the bacterial signatures in periodontitis and chronic obstructive pulmonary disease (COPD). MATERIALS AND METHODS: We collected subgingival plaque and gingival crevicular fluid samples from 112 individuals (31 healthy controls, 24 patients with periodontitis, 28 patients with COPD, and 29 patients with both periodontitis and COPD). The oral microbiota was analyzed using 16S rRNA gene sequencing and diversity and functional prediction analysis were performed. RESULTS: We observed higher bacterial richness in individuals with periodontitis in both types of oral samples. Using LEfSe and DESeq2 analyses, we found differentially abundant genera that may be potential biomarkers for each group. Mogibacterium is the predominant genus in COPD. Ten genera, including Desulfovibrio, Filifactor, Fretibacterium, Moraxella, Odoribacter, Pseudoramibacter Pyramidobacter, Scardovia, Shuttleworthia and Treponema were predominant in periodontitis. Bergeyella, Lautropia, Rothia, Propionibacterium and Cardiobacterium were the signature of the healthy controls. The significantly different pathways in the Kyoto Encyclopedia of Genes and Genomes (KEGG) between healthy controls and other groups were concentrated in genetic information processing, translation, replication and repair, and metabolism of cofactors and vitamins. CONCLUSIONS: We found the significant differences in the bacterial community and functional characterization of oral microbiota in periodontitis, COPD and comorbid diseases. Compared to gingival crevicular fluid, subgingival plaque may be more appropriate for reflecting the difference of subgingival microbiota in periodontitis patients with COPD. These results may provide potentials for predicting, screening, and treatment strategies for individuals with periodontitis and COPD.
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spelling pubmed-99480372023-02-24 Oral microbial dysbiosis in patients with periodontitis and chronic obstructive pulmonary disease Liu, Siqin Xie, Guofang Chen, Meifeng He, Yukun Yu, Wenyi Chen, Xiaobo Mao, Weigang Liu, Nanxia Zhang, Yuanjie Chang, Qin Qiao, Yingying Ma, Xinqian Xue, Jianbo Jin, Mengtong Guo, Shuming Hou, Yudong Gao, Zhancheng Front Cell Infect Microbiol Cellular and Infection Microbiology BACKGROUND: Oral microbiota is closely related to the homeostasis of the oral cavity and lungs. To provide potential information for the prediction, screening, and treatment strategies of individuals, this study compared and investigated the bacterial signatures in periodontitis and chronic obstructive pulmonary disease (COPD). MATERIALS AND METHODS: We collected subgingival plaque and gingival crevicular fluid samples from 112 individuals (31 healthy controls, 24 patients with periodontitis, 28 patients with COPD, and 29 patients with both periodontitis and COPD). The oral microbiota was analyzed using 16S rRNA gene sequencing and diversity and functional prediction analysis were performed. RESULTS: We observed higher bacterial richness in individuals with periodontitis in both types of oral samples. Using LEfSe and DESeq2 analyses, we found differentially abundant genera that may be potential biomarkers for each group. Mogibacterium is the predominant genus in COPD. Ten genera, including Desulfovibrio, Filifactor, Fretibacterium, Moraxella, Odoribacter, Pseudoramibacter Pyramidobacter, Scardovia, Shuttleworthia and Treponema were predominant in periodontitis. Bergeyella, Lautropia, Rothia, Propionibacterium and Cardiobacterium were the signature of the healthy controls. The significantly different pathways in the Kyoto Encyclopedia of Genes and Genomes (KEGG) between healthy controls and other groups were concentrated in genetic information processing, translation, replication and repair, and metabolism of cofactors and vitamins. CONCLUSIONS: We found the significant differences in the bacterial community and functional characterization of oral microbiota in periodontitis, COPD and comorbid diseases. Compared to gingival crevicular fluid, subgingival plaque may be more appropriate for reflecting the difference of subgingival microbiota in periodontitis patients with COPD. These results may provide potentials for predicting, screening, and treatment strategies for individuals with periodontitis and COPD. Frontiers Media S.A. 2023-02-09 /pmc/articles/PMC9948037/ /pubmed/36844402 http://dx.doi.org/10.3389/fcimb.2023.1121399 Text en Copyright © 2023 Liu, Xie, Chen, He, Yu, Chen, Mao, Liu, Zhang, Chang, Qiao, Ma, Xue, Jin, Guo, Hou and Gao 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 Cellular and Infection Microbiology
Liu, Siqin
Xie, Guofang
Chen, Meifeng
He, Yukun
Yu, Wenyi
Chen, Xiaobo
Mao, Weigang
Liu, Nanxia
Zhang, Yuanjie
Chang, Qin
Qiao, Yingying
Ma, Xinqian
Xue, Jianbo
Jin, Mengtong
Guo, Shuming
Hou, Yudong
Gao, Zhancheng
Oral microbial dysbiosis in patients with periodontitis and chronic obstructive pulmonary disease
title Oral microbial dysbiosis in patients with periodontitis and chronic obstructive pulmonary disease
title_full Oral microbial dysbiosis in patients with periodontitis and chronic obstructive pulmonary disease
title_fullStr Oral microbial dysbiosis in patients with periodontitis and chronic obstructive pulmonary disease
title_full_unstemmed Oral microbial dysbiosis in patients with periodontitis and chronic obstructive pulmonary disease
title_short Oral microbial dysbiosis in patients with periodontitis and chronic obstructive pulmonary disease
title_sort oral microbial dysbiosis in patients with periodontitis and chronic obstructive pulmonary disease
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9948037/
https://www.ncbi.nlm.nih.gov/pubmed/36844402
http://dx.doi.org/10.3389/fcimb.2023.1121399
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