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Metagenomic characterization of the microbiomes in five different body habitats of otherwise healthy individuals with periodontal disease

INTRODUCTION: Recent studies have proposed several plausible mechanisms supporting the association between periodontal disease and systemic disease. However, characterizing the microbial communities in individuals with periodontal disease before onset of other diseases is an important first step in...

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Autores principales: Oh, Sujin, Lee, Hyo-Jung, Park, Kyoung Un
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10534035/
https://www.ncbi.nlm.nih.gov/pubmed/37780855
http://dx.doi.org/10.3389/fcimb.2023.1257816
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author Oh, Sujin
Lee, Hyo-Jung
Park, Kyoung Un
author_facet Oh, Sujin
Lee, Hyo-Jung
Park, Kyoung Un
author_sort Oh, Sujin
collection PubMed
description INTRODUCTION: Recent studies have proposed several plausible mechanisms supporting the association between periodontal disease and systemic disease. However, characterizing the microbial communities in individuals with periodontal disease before onset of other diseases is an important first step in determining how the altered microbial state contributes to disease progression. This study established microbiome profiles for five body habitats of carefully selected, otherwise healthy individuals with periodontal disease. METHODS: Blood, oral (buccal mucosa, dental plaque, and saliva), and stool samples were collected from ten healthy subjects with periodontal disease. Using 16S rRNA metagenomics, the taxonomic and functional compositions of microbiomes were investigated. RESULTS: The most predominant phylum in blood and stool was Bacillota. Pseudomonadota accounted for the largest proportion of microbes in the buccal mucosa and saliva, whereas Bacteroidota were the most prevalent in dental plaque. Differential abundance analysis revealed that 12 phyla and 139 genera were differentially abundant between body habitats. Comparison of alpha diversity showed that the blood microbiome has the most diverse community close to neither oral nor stool microbiomes. We also predicted the functional configurations of the microbiome in otherwise healthy subjects with periodontal disease. Principal coordinate analysis based on functional abundance revealed distinct clustering of the microbial communities between different body habitats, as also observed for taxonomic abundance. In addition, 13 functional pathways, including lipopolysaccharide biosynthesis, glutathione metabolism, and proteasome, showed differential expression between habitats. DISCUSSION: Our results offer insight into the effects of the microbiome on systemic health and disease in people with periodontal disease.
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spelling pubmed-105340352023-09-29 Metagenomic characterization of the microbiomes in five different body habitats of otherwise healthy individuals with periodontal disease Oh, Sujin Lee, Hyo-Jung Park, Kyoung Un Front Cell Infect Microbiol Cellular and Infection Microbiology INTRODUCTION: Recent studies have proposed several plausible mechanisms supporting the association between periodontal disease and systemic disease. However, characterizing the microbial communities in individuals with periodontal disease before onset of other diseases is an important first step in determining how the altered microbial state contributes to disease progression. This study established microbiome profiles for five body habitats of carefully selected, otherwise healthy individuals with periodontal disease. METHODS: Blood, oral (buccal mucosa, dental plaque, and saliva), and stool samples were collected from ten healthy subjects with periodontal disease. Using 16S rRNA metagenomics, the taxonomic and functional compositions of microbiomes were investigated. RESULTS: The most predominant phylum in blood and stool was Bacillota. Pseudomonadota accounted for the largest proportion of microbes in the buccal mucosa and saliva, whereas Bacteroidota were the most prevalent in dental plaque. Differential abundance analysis revealed that 12 phyla and 139 genera were differentially abundant between body habitats. Comparison of alpha diversity showed that the blood microbiome has the most diverse community close to neither oral nor stool microbiomes. We also predicted the functional configurations of the microbiome in otherwise healthy subjects with periodontal disease. Principal coordinate analysis based on functional abundance revealed distinct clustering of the microbial communities between different body habitats, as also observed for taxonomic abundance. In addition, 13 functional pathways, including lipopolysaccharide biosynthesis, glutathione metabolism, and proteasome, showed differential expression between habitats. DISCUSSION: Our results offer insight into the effects of the microbiome on systemic health and disease in people with periodontal disease. Frontiers Media S.A. 2023-09-13 /pmc/articles/PMC10534035/ /pubmed/37780855 http://dx.doi.org/10.3389/fcimb.2023.1257816 Text en Copyright © 2023 Oh, Lee and Park 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
Oh, Sujin
Lee, Hyo-Jung
Park, Kyoung Un
Metagenomic characterization of the microbiomes in five different body habitats of otherwise healthy individuals with periodontal disease
title Metagenomic characterization of the microbiomes in five different body habitats of otherwise healthy individuals with periodontal disease
title_full Metagenomic characterization of the microbiomes in five different body habitats of otherwise healthy individuals with periodontal disease
title_fullStr Metagenomic characterization of the microbiomes in five different body habitats of otherwise healthy individuals with periodontal disease
title_full_unstemmed Metagenomic characterization of the microbiomes in five different body habitats of otherwise healthy individuals with periodontal disease
title_short Metagenomic characterization of the microbiomes in five different body habitats of otherwise healthy individuals with periodontal disease
title_sort metagenomic characterization of the microbiomes in five different body habitats of otherwise healthy individuals with periodontal disease
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10534035/
https://www.ncbi.nlm.nih.gov/pubmed/37780855
http://dx.doi.org/10.3389/fcimb.2023.1257816
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