Exploration of the interplay between spatially distinct microbial habitats through comparative analysisopen access
- Authors
- Kim, Hyunji; Hong, Jin-Sil; Yun, Pil-Young; Hwang, Kyung-Gyun; Kim, Keun-Suh; Lee, Hyo-Jung; Park, Kyoung Un
- Issue Date
- Dec-2023
- Publisher
- Co-Action Publishing
- Keywords
- Microbiome; habitat; saliva; blood; plaque; genomics; periodontitis
- Citation
- Journal of Oral Microbiology, v.15, no.1, pp 1 - 13
- Pages
- 13
- Indexed
- SCIE
SCOPUS
- Journal Title
- Journal of Oral Microbiology
- Volume
- 15
- Number
- 1
- Start Page
- 1
- End Page
- 13
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/188419
- DOI
- 10.1080/20002297.2023.2229693
- ISSN
- 2000-2297
2000-2297
- Abstract
- 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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