Literature DB >> 33425781

Discriminating Microbial Community Structure Between Peri-Implantitis and Periodontitis With Integrated Metagenomic, Metatranscriptomic, and Network Analysis.

Keiji Komatsu1, Takahiko Shiba1, Yasuo Takeuchi1, Takayasu Watanabe2, Tatsuro Koyanagi1, Takashi Nemoto1, Masahiro Shimogishi3, Masaki Shibasaki3, Sayaka Katagiri1, Shohei Kasugai3, Takanori Iwata1.   

Abstract

Peri-implantitis and periodontitis are both polymicrobial diseases induced by subgingival plaque accumulation, with some differing clinical features. Studies on the microbial and gene transcription activity of peri-implantitis microbiota are limited. This study aimed to verify the hypothesis that disease-specific microbial and gene transcription activity lead to disease-specific clinical features, using an integrated metagenomic, metatranscriptomic, and network analysis. Metagenomic data in peri-implantitis and periodontitis were obtained from the same 21 subjects and metatranscriptomic data from 12 subjects were obtained from a database. The microbial co-occurrence network based on metagenomic analysis had more diverse species taxa and correlations than the network based on the metatranscriptomic analysis. Solobacterium moorei and Prevotella denticola had high activity and were core species taxa specific to peri-implantitis in the co-occurrence network. Moreover, the activity of plasmin receptor/glyceraldehyde-3-phosphate dehydrogenase genes was higher in peri-implantitis. These activity differences may increase complexity in the peri-implantitis microbiome and distinguish clinical symptoms of the two diseases. These findings should help in exploring a novel biomarker that assist in the diagnosis and preventive treatment design of peri-implantitis.
Copyright © 2020 Komatsu, Shiba, Takeuchi, Watanabe, Koyanagi, Nemoto, Shimogishi, Shibasaki, Katagiri, Kasugai and Iwata.

Entities:  

Keywords:  dysbiosis; metagenome; metatranscriptome; oral microbiome; peri-implantitis; periodontitis

Year:  2020        PMID: 33425781      PMCID: PMC7793907          DOI: 10.3389/fcimb.2020.596490

Source DB:  PubMed          Journal:  Front Cell Infect Microbiol        ISSN: 2235-2988            Impact factor:   5.293


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