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Molecular biological analysis of oral bacterial population dynamics

Research Project

Project/Area Number 10671699
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Morphological basic dentistry
Research InstitutionOkayama University

Principal Investigator

FUKUI Kazuhiro  Okayama University Dental School, Professor, 歯学部, 教授 (70034171)

Co-Investigator(Kenkyū-buntansha) SHINGAKI Ryuuji  Okayama University Dental School, Assistant, 歯学部, 助手 (40294417)
TANIMOTO Ichiro  Okayama University Dental School, Assistant, 歯学部, 助手 (00280686)
INOUE Tetsuyoshi  Okayama University Dental School, Assistant, 歯学部, 助手 (20223258)
井上 美穂  岡山大学, 歯学部, 教務員 (20271059)
Project Period (FY) 1998 – 2000
Project Status Completed (Fiscal Year 2000)
Budget Amount *help
¥3,300,000 (Direct Cost: ¥3,300,000)
Fiscal Year 2000: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 1999: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 1998: ¥1,400,000 (Direct Cost: ¥1,400,000)
Keywordsbacterial community / 16SrDNA / PCR / dental caries / periodontal bacteria / 齲蝕 / genotype / 口腔細菌 / 16S rRNA
Research Abstract

1 Carious dentine and dental plaque bacterial communities were analyzed by the culture-independent molecular biological method. PCR amplification and DNA sequencing of 16SrDNA showed variety of bacterial existence, including organisms less isolated from oral cavity or ones with no sequence homology to the databank registered bacteria. Additionally, bacterial population difference between initial and progressed stage of caries was shown. In the shallow carious dentine bacteria represented Streptococcus, Actinomyces, similar to the plaque sample were detected, but in the deeply progressed carious dentine Lactobacillus was dominant, suggesting that there is a significant change of bacterial population accompanied with the dental caries progression. In this study, we analyzed carious dentine samples from 3 different patients. Of all samples, detection rates of strong carious causative agents such as S.mutant or S.sobrinus are extremely low or zero, which may suggest that various oral bacteria are related to the progression of dental caries.
2 In order to detect the specific bacteria from contaminated specimens, we attempted the PCR detection of periodontal pathogens, Actinobacillus actionomycetemcomitans and Porphromonas gingivalis from dental plaque sample of 60 young healthy volunteers. Through 3 years of investigation, against the distinct groups of volunteers, Actinobacillus actionomycetemcomitans, which was not able to be isolated on the selectively media culture, was detected in ratio 20 to 30%.
As the above mentioned, analysis using molecular biological culture-independent method brought a new kind of knowledge about the oral bacterial communities.

Report

(4 results)
  • 2000 Annual Research Report   Final Research Report Summary
  • 1999 Annual Research Report
  • 1998 Annual Research Report
  • Research Products

    (5 results)

All Other

All Publications (5 results)

  • [Publications] 橋本武: "齲蝕細菌叢の分析への分子系統学的手法の応用"岡山歯学会雑誌. 18巻・1号. 203-218 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] 新垣隆資: "PCR法による歯周病原生細菌の検出"医学と生物学. 141巻・2号. 51-54 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] HASHIMOTI, T.: "Phylogenetic analysis of the carious dentine bacterial community."The journal of Okayama dental society. 18, 1. 203-218 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] SHINGAKI, R.: "PCR detection of periodontal pathogens from dental plaque."Medicine and Biology. 141, 2. 51-54 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] 新垣隆資: "PCR法による歯周病原生細菌の検出"医学と生物学. 14巻・2号. 51-54 (2000)

    • Related Report
      2000 Annual Research Report

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Published: 1998-04-01   Modified: 2016-04-21  

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