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Exploration of the interplay between spatially distinct microbial habitats through comparative analysis

OBJECTIVES: The oral microbiome is closely associated with systemic diseases, indicating the presence of bacteremia and inflammatory mediators in the systemic circulation. Our research aims to investigate the relationship between the oral microbiome and other microbial habitats. METHODS: We analyzed...

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Autores principales: Kim, Hyunji, Hong, Jin-Sil, Yun, Pil-Young, Hwang, Kyung-Gyun, Kim, Keun-Suh, Lee, Hyo-Jung, Park, Kyoung Un
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10308874/
https://www.ncbi.nlm.nih.gov/pubmed/37396300
http://dx.doi.org/10.1080/20002297.2023.2229693
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author Kim, Hyunji
Hong, Jin-Sil
Yun, Pil-Young
Hwang, Kyung-Gyun
Kim, Keun-Suh
Lee, Hyo-Jung
Park, Kyoung Un
author_facet Kim, Hyunji
Hong, Jin-Sil
Yun, Pil-Young
Hwang, Kyung-Gyun
Kim, Keun-Suh
Lee, Hyo-Jung
Park, Kyoung Un
author_sort Kim, Hyunji
collection PubMed
description OBJECTIVES: The oral microbiome is closely associated with systemic diseases, indicating the presence of bacteremia and inflammatory mediators in the systemic circulation. Our research aims to investigate the relationship between the oral microbiome and other microbial habitats. METHODS: We analyzed 180 specimens from 36 patients, including saliva, buccal swab, plaque, stool, and blood samples from a healthy group (Non_PD, n = 18) and a periodontitis group (PD, n = 18). The final analysis included 147 specimens, with varying sample sizes for each group. Metagenomic analysis was performed using prokaryotic 16S rRNA on the MiSeq platform (Illumina). RESULTS: PD saliva showed significant richness differences (P's < 0.05), similar to plaque. Buccal swabs had slight variations. Microbial network analysis revealed altered microbial interactions in the PD group, with decreased interactions in saliva and buccal swabs, and increased interactions in plaque. In our analysis of nine specimens where all paired habitat samples could be analyzed, microorganisms linked to oral periodontitis were found in sterile blood samples, resembling the oral cavity's composition. CONCLUSIONS: Microbiome differences should consider overall microbial-environment interactions, alongside diversity and richness. Our data cautiously suggest that disease-related changes in the salivary microbiome may be reflected in blood specimens through the oral-blood axis.
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spelling pubmed-103088742023-06-30 Exploration of the interplay between spatially distinct microbial habitats through comparative analysis Kim, Hyunji Hong, Jin-Sil Yun, Pil-Young Hwang, Kyung-Gyun Kim, Keun-Suh Lee, Hyo-Jung Park, Kyoung Un J Oral Microbiol AC-Microbiome Modulators and Oral Health OBJECTIVES: The oral microbiome is closely associated with systemic diseases, indicating the presence of bacteremia and inflammatory mediators in the systemic circulation. Our research aims to investigate the relationship between the oral microbiome and other microbial habitats. METHODS: We analyzed 180 specimens from 36 patients, including saliva, buccal swab, plaque, stool, and blood samples from a healthy group (Non_PD, n = 18) and a periodontitis group (PD, n = 18). The final analysis included 147 specimens, with varying sample sizes for each group. Metagenomic analysis was performed using prokaryotic 16S rRNA on the MiSeq platform (Illumina). RESULTS: PD saliva showed significant richness differences (P's < 0.05), similar to plaque. Buccal swabs had slight variations. Microbial network analysis revealed altered microbial interactions in the PD group, with decreased interactions in saliva and buccal swabs, and increased interactions in plaque. In our analysis of nine specimens where all paired habitat samples could be analyzed, microorganisms linked to oral periodontitis were found in sterile blood samples, resembling the oral cavity's composition. CONCLUSIONS: Microbiome differences should consider overall microbial-environment interactions, alongside diversity and richness. Our data cautiously suggest that disease-related changes in the salivary microbiome may be reflected in blood specimens through the oral-blood axis. Taylor & Francis 2023-06-27 /pmc/articles/PMC10308874/ /pubmed/37396300 http://dx.doi.org/10.1080/20002297.2023.2229693 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle AC-Microbiome Modulators and Oral Health
Kim, Hyunji
Hong, Jin-Sil
Yun, Pil-Young
Hwang, Kyung-Gyun
Kim, Keun-Suh
Lee, Hyo-Jung
Park, Kyoung Un
Exploration of the interplay between spatially distinct microbial habitats through comparative analysis
title Exploration of the interplay between spatially distinct microbial habitats through comparative analysis
title_full Exploration of the interplay between spatially distinct microbial habitats through comparative analysis
title_fullStr Exploration of the interplay between spatially distinct microbial habitats through comparative analysis
title_full_unstemmed Exploration of the interplay between spatially distinct microbial habitats through comparative analysis
title_short Exploration of the interplay between spatially distinct microbial habitats through comparative analysis
title_sort exploration of the interplay between spatially distinct microbial habitats through comparative analysis
topic AC-Microbiome Modulators and Oral Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10308874/
https://www.ncbi.nlm.nih.gov/pubmed/37396300
http://dx.doi.org/10.1080/20002297.2023.2229693
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