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Oral‐gut bacterial profiles discriminate between periodontal health and diseases

失调 肠道菌群 牙周炎 核梭杆菌 牙龈炎 粪便 聚集放线菌 唾液 微生物群 生物 微生物学 梭杆菌 口腔微生物群 拟杆菌 医学 免疫学 内科学 细菌 牙科 牙龈卟啉单胞菌 生物信息学 遗传学
作者
Talita Gomes Baêta Lourenço,Adriana Miranda de Oliveira,Tsute Chen,Ana Paula Vieira Colombo
出处
期刊:Journal of Periodontal Research [Wiley]
卷期号:57 (6): 1227-1237 被引量:4
标识
DOI:10.1111/jre.13059
摘要

Abstract Objective This investigation explored oral‐gut microbial signatures with potential to distinguish among periodontal conditions. Background Data The interplay between the oral and gut microbiomes may be a critical pathway linking periodontal diseases and systemic inflammatory disorders. The mechanisms by which oral microorganisms translocate to the gut and cause microbial dysbiosis, favoring an inflammatory state, are still unknown. As a first approach, characterization of oral‐gut microbial profiles associated with periodontal health and diseases can provide insights on such mechanisms of etiology and pathogenesis. Methods Fecal and saliva samples from individuals with periodontal health (PH, 8), gingivitis (GG, 17), and periodontitis (PD, 24) were analyzed for their microbial composition by 16S rRNA gene sequencing. Microbial taxa were compared and correlated to periodontal parameters. Multivariate discriminant analysis (MDA) was carried out to identify profiles related to health and disease. Results Few significant differences in oral‐gut taxa were detected among clinical groups, although increase in fecal Fusobacterium nucleatum ss vincentii and salivary Aggregatibacter actinomycetemcomitans , Parvimonas micra , and Fretibacterium sp. HMT358 were strongly correlated with deep pockets and inflammation ( p < .01). Over 50% of the fecal microbiota comprised microorganisms shared between oral and gut sites, whereas oral taxa were detected in approximately 9%, particularly enriched in GG fecal samples ( p = .04). Trends for lower fecal richness and higher salivary diversity in PD compared to PH were observed. MDA was able to classify correctly 82% of the patients into the clinical groups. Main classifiers of periodontitis were high BMI, older age, and enrichment of oral‐fecal Leptotrichia sp. HMT4, Peptostreptococcus stomatis , Dialister invisus , and a novel Lautropia sp. HMTC89‐like organism. Conclusion Within the limitations of an exploratory investigation, specific profiles of oral‐gut taxa, including known and potential novel organisms, combined with social‐demographic features were able to discriminate individuals with periodontal diseases in this study population.
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