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2005 Fiscal Year Final Research Report Summary

Resolution of quorum-sensing systems in dental plaque biofilm and development of the method that prevents the plaque formation by the control of them

Research Project

Project/Area Number 16592050
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Orthodontic/Pediatric dentistry
Research InstitutionNagasaki University

Principal Investigator

HOSHINO Tomonori  Nagasaki University, Graduate School of Biomedical Sciences, Research assistant, 大学院・医歯薬学総合研究科, 助手 (00359960)

Co-Investigator(Kenkyū-buntansha) FUJIWARA Taku  Nagasaki University, Graduate School of Biomedical Sciences, Professor, 大学院・医歯薬学総合研究科, 教授 (00228975)
KUBOTA Kazumi  Nagasaki University, Hospital of Medicine and Dentistry, Instructor, 医学部・歯学部附属病院, 講師 (30240914)
SHINKAWA Hiroe  Nagasaki University, Graduate School of Biomedical Sciences, Research assistant, 大学院・医歯薬学総合研究科, 助手 (60346921)
Project Period (FY) 2004 – 2005
Keywordsmutans group streptococci / biofilm / quorum-sensing / mitis group streptococci / alpha-hemolytic bacteria
Research Abstract

Dental plaque is the biofilm which is formed on the tooth surface, and is a protective barrier for the bacteria against the change of the environment, the antibiotic, and the host immune response. First this biofilm is formed by the extracellular polysaccharide (glucan), which the mitis group streptococci produce from sugar, and then is reinforced by the adhesive and water-insoluble glucan, which the mutans group streptococci produce. Dental plaque biofilm plays an important role in the caries formation. In this biofilm, the plaque bacteria communicate with other bacteria by the auto-inducer like hormone. By this communication system that is commonly known as quorum-sensing, the bacterial population density in the dental plaque is thought to be kept constant, and the bacterial mass against the host immune system is constructed.
In the present study, to solve the quorum-sensing system in the dental plaque, we developed the method to identify the oral streptococci, which were the members of this biofilm. This method could rapidly identify the streptococci which were dominant and occupied 60% in the oral flora. We published the paper about it entitled "Method for rapid identification of oral streptococci by PCR using 16S-23S ribosomal RNA intergenic spacer". On the other hand, we investigated the longitudinal study of oral flora against the 2 predentate infants and the cross-sectional study of oral flora against the 40 nursery school students (aged 1 to 4 years old). As a result, we demonstrated that the rate of alpha-hemolytic bacteria in oral flora decreased by the inhabitation of the mutans streptococci, suggested that the quorum-sensing system between mutans streptococci and alpha-hemolytic bacteria existed. We had submitted the paper about this entitled "Establishment of S.mutans Change Salivary Bacterial ratio".
Our future study is to identify auto-inducer produced between mutans streptococci and alpha-hemolytic bacteria.

  • Research Products

    (1 results)

All 2005

All Journal Article (1 results)

  • [Journal Article] Method for rapid identification of oral streptococci by PCR using 16S-23S ribosomal RNA intergenic spacer2005

    • Author(s)
      Tomonori Hoshino
    • Journal Title

      Pediatric Dental Journal 15(2)

      Pages: 185-190

    • Description
      「研究成果報告書概要(和文)」より

URL: 

Published: 2007-12-13  

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