Microbial Communities and Functional Genes in Periodontitis and Healthy Controls.

16S rRNA Case-control study PICRUSt Periodontitis Saliva microbiome

Journal

International dental journal
ISSN: 1875-595X
Titre abrégé: Int Dent J
Pays: England
ID NLM: 0374714

Informations de publication

Date de publication:
05 Mar 2024
Historique:
received: 29 08 2023
revised: 05 01 2024
accepted: 17 01 2024
medline: 7 3 2024
pubmed: 7 3 2024
entrez: 6 3 2024
Statut: aheadofprint

Résumé

Periodontitis is a chronic progressive disease and the leading cause of tooth loss in adults. Recent studies have shown the impact of oral microbial communities on systemic health and diseases such as cancer, atherosclerosis, rheumatoid arthritis, inflammatory bowel disease, diabetes, hypertension, and Alzheimer's disease. In previous case control studies investigatin the relationship between periodontal disease and the oral microbiota, little attention has been paid to the intersections of these domains. Here, we used high-throughput 16S rRNA sequencing to analyse the differences in the microbial composition in saliva between a group of patients with chronic periodontitis (C; n = 51) and a healthy control group (H; n = 61) and predicted the functional gene composition by Phylogenetic Investigation of Communities by Reconstruction of Unobserved States. We found significant alterations in oral microbial diversity between C and H (P = 0.002). Sixteen genera were significantly different between C and H, and 15 of them were enriched in C linear discriminant analysis (LDA > 2). Fifty functional genes were significantly different between C and H, and 34 of them were enriched in C (P < .025). Periodontitis is associated with significant changes in the oral microbial community.

Sections du résumé

BACKGROUND BACKGROUND
Periodontitis is a chronic progressive disease and the leading cause of tooth loss in adults. Recent studies have shown the impact of oral microbial communities on systemic health and diseases such as cancer, atherosclerosis, rheumatoid arthritis, inflammatory bowel disease, diabetes, hypertension, and Alzheimer's disease. In previous case control studies investigatin the relationship between periodontal disease and the oral microbiota, little attention has been paid to the intersections of these domains.
METHODS METHODS
Here, we used high-throughput 16S rRNA sequencing to analyse the differences in the microbial composition in saliva between a group of patients with chronic periodontitis (C; n = 51) and a healthy control group (H; n = 61) and predicted the functional gene composition by Phylogenetic Investigation of Communities by Reconstruction of Unobserved States.
RESULTS RESULTS
We found significant alterations in oral microbial diversity between C and H (P = 0.002). Sixteen genera were significantly different between C and H, and 15 of them were enriched in C linear discriminant analysis (LDA > 2). Fifty functional genes were significantly different between C and H, and 34 of them were enriched in C (P < .025).
CONCLUSIONS CONCLUSIONS
Periodontitis is associated with significant changes in the oral microbial community.

Identifiants

pubmed: 38448300
pii: S0020-6539(24)00037-6
doi: 10.1016/j.identj.2024.01.012
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest None disclosed.

Auteurs

Zhonghui Ma (Z)

Department of Stomatology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China; Gene Hospital of Henan Province, Precision Medicine Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

Ze Jiang (Z)

Department of Stomatology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

Haoxin Dong (H)

Department of Stomatology, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou, China.

Wenhua Xu (W)

Department of Stomatology, Zhengzhou People's Hospital, Zhengzhou, China.

Su Yan (S)

Health Management Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

Jingfeng Chen (J)

Health Management Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

Ang Li (A)

Gene Hospital of Henan Province, Precision Medicine Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China. Electronic address: lia@zju.edu.cn.

Xi Wang (X)

Department of Stomatology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China. Electronic address: fccwangx1@zzu.edu.cn.

Classifications MeSH