Abstract

Dental implants are commonly used to replace missing teeth. However, the dysbiotic polymicrobial communities of peri-implant sites are responsible for peri-implant diseases, such as peri-implant mucositis and peri-implantitis. In this study, we analyzed the microbial characteristics of oral plaque from peri-implant pockets or sulci of healthy implants (n = 10), peri-implant mucositis (n = 8) and peri-implantitis (n = 6) sites using pyrosequencing of the 16S rRNA gene. An increase in microbial diversity was observed in subgingival sites of ailing implants, compared with healthy implants. Microbial co-occurrence analysis revealed that periodontal pathogens, such as Porphyromonas gingivalis, Tannerella forsythia, and Prevotella intermedia, were clustered into modules in the peri-implant mucositis network. Putative pathogens associated with peri-implantitis were present at a moderate relative abundance in peri-implant mucositis, suggesting that peri-implant mucositis an important early transitional phase during the development of peri-implantitis. Furthermore, the relative abundance of Eubacterium was increased at peri-implantitis locations, and co-occurrence analysis revealed that Eubacterium minutum was correlated with Prevotella intermedia in peri-implantitis sites, which suggests the association of Eubacterium with peri-implantitis. This study indicates that periodontal pathogens may play important roles in the shifting of healthy implant status to peri-implant disease.

Highlights

  • After implant placement to establish polymicrobial communities[9,10], and the failure of dental implants is commonly ascribed to inflammation of the supporting bone and related soft tissues caused by microbiota in peri-implant biofilms[11,12]

  • We measured the complexity of microbial communities in PI sites, which contained larger numbers of operational taxonomic units (OTUs) and had higher Shannon index values than did healthy implant sites

  • In recent work using the 16S rRNA gene pyrosequencing method[31], no significant difference in the microbial diversity of healthy and ailing implants was found, which is in part explained by the fact that peri-implant mucositis (PM) and PI patients were both assigned to the diseased group

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Summary

Introduction

After implant placement to establish polymicrobial communities[9,10], and the failure of dental implants is commonly ascribed to inflammation of the supporting bone and related soft tissues caused by microbiota in peri-implant biofilms[11,12]. Studies on the pathogenesis of peri-implant microbiota have analyzed individual bacterial species in complex microbial communities. Previous studies, using culture-based methods, 16S rRNA gene PCR, or DNA-DNA hybridization techniques, commonly addressed roles played by individual bacterial species and afforded limited information on the overall diversity of the peri-implant environment. Pyrosequencing of PCR-amplified 16S rRNA is a next-generation sequencing method that simultaneously generates thousands of sequences from individual samples Such an unprecedented amount of information allows comprehensive examination of a taxonomically heterogeneous community and has revealed ever-greater levels of microbial diversity[20,21]. This study was performed to compare the differences of the microbial communities of healthy implants, PM and PI, aiming to reveal the potential pathogens associated with peri-implant diseases

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