Abstract

Development of dental plaque begins with the adhesion of salivary bacteria to the acquired pellicle covering the tooth surface. In this study, we collected in vivo dental plaque formed on hydroxyapatite disks for 6 h from 74 young adults and identified initial colonizing taxa based on full-length 16S rRNA gene sequences. A long-read, single-molecule sequencer, PacBio Sequel, provided 100,109 high-quality full-length 16S rRNA gene sequence reads from the early plaque microbiota, which were assigned to 90 oral bacterial taxa. The microbiota obtained from every individual mostly comprised the 21 predominant taxa with the maximum relative abundance of over 10% (95.8 ± 6.2%, mean ± SD), which included Streptococcus species as well as nonstreptococcal species. A hierarchical cluster analysis of their relative abundance distribution suggested three major patterns of microbiota compositions: a Streptococcus mitis/Streptococcus sp. HMT-423-dominant profile, a Neisseria sicca/Neisseria flava/Neisseria mucosa-dominant profile, and a complex profile with high diversity. No notable variations in the community structures were associated with the dental caries status, although the total bacterial amounts were larger in the subjects with a high number of caries-experienced teeth (≥8) than in those with no or a low number of caries-experienced teeth. Our results revealed the bacterial taxa primarily involved in early plaque formation on hydroxyapatite disks in young adults.IMPORTANCE Selective attachment of salivary bacteria to the tooth surface is an initial and repetitive phase in dental plaque development. We employed full-length 16S rRNA gene sequence analysis with a high taxonomic resolution using a third-generation sequencer, PacBio Sequel, to determine the bacterial composition during early plaque formation in 74 young adults accurately and in detail. The results revealed 21 bacterial taxa primarily involved in early plaque formation on hydroxyapatite disks in young adults, which include several streptococcal species as well as nonstreptococcal species, such as Neisseria sicca/N flava/N mucosa and Rothia dentocariosa Given that no notable variations in the microbiota composition were associated with the dental caries status, the maturation process, rather than the specific bacterial species that are the initial colonizers, is likely to play an important role in the development of dysbiotic microbiota associated with dental caries.

Highlights

  • Development of dental plaque begins with the adhesion of salivary bacteria to the acquired pellicle covering the tooth surface

  • This study investigated the bacterial composition of early dental plaque of 74 participants (38 females and 36 males) aged from 20 to 32 years having at least 24 teeth

  • To confirm that the obtained plaque samples were not salivary bacterial populations that were washed onto the disk, the microbiota composition of early plaque samples was compared with that of saliva samples based on the V1-V2 regions of 16S rRNA gene sequence data provided by the second-generation sequencer msystems.asm.org 2

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Summary

Introduction

Development of dental plaque begins with the adhesion of salivary bacteria to the acquired pellicle covering the tooth surface. We collected in vivo dental plaque formed on hydroxyapatite disks for 6 h from 74 young adults and identified initial colonizing taxa based on full-length 16S rRNA gene sequences. Multiple studies have identified earlycolonizing taxa capable of attaching to the acquired pellicle covering the enamel, which has been accomplished using several different approaches, such as cultivation [4], a checkerboard hybridization technique [5], an oral microbe identification microarray [6], a microarray and a culture collection [7], and an 16S rRNA gene clone library [8] These studies consistently demonstrated that the early plaque microbiota is constituted primarily by Streptococcus species, in particular Streptococcus mitis and Streptococcus oralis, with a subset of nonstreptococcal species, such as Neisseria, Rothia, and Gemella. With the latest model of this platform, Sequel achieved approximately a throughput gain of ϳ7ϫ, allowing for a much deeper sequence depth than the previous model (RS II)

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