Quantitative real-time PCR using TaqMan and SYBR Green for Actinobacillus actinomycetemcomitans, Porphyromonas gingivalis, Prevotella intermedia, tetQ gene and total bacteria

Hiroshi Maeda, Chiyo Fujimoto, Yasuhiro Haruki, Takemasa Maeda, Susumu Kokeguchi, Millan Petelin, Hideo Arai, Ichiro Tanimoto, Fusanori Nishimura, Shogo Takashiba

Research output: Contribution to journalArticle

298 Citations (Scopus)

Abstract

Accurate quantification of bacterial species in dental plaque is needed for microbiological diagnosis of periodontal diseases. The present study was designed to assess the sensitivity, specificity and quantitativity of the real-time PCR using the GeneAmpR Sequence Detection System with two fluorescence chemistries. TaqMan probe with reporter and quencher dye, and SYBR Green dye were used for sources of the fluorescence. Primers and probes were designed for Actinobacillus actinomycetemcomitans, Porphyromonas gingivalis, Prevotella intermedia and total bacteria based on the nucleotide sequences of the respective 16S ribosomal RNA genes. Since spread of antibiotic resistance genes is one of the crucial problems in periodontal therapy, quantitative detection of tetQ gene, which confers resistance to tetracycline, was included in the examination. The detection of P. gingivalis, P. intermedia and A. actinomycetemcomitans was linear over a range of 10-107 cells (10-107 copies for tetQ gene), while the quantitative range for total bacteria was 102-107 cells. Species-specific amplifications were observed for the three periodontal bacteria, and there was no significant difference between the TaqMan and SYBR Green chemistry in their specificity, quantitativity and sensitivity. The SYBR Green assay, which was simpler than TaqMan assay in its manipulations, was applied to the clinical plaque samples. The plaque samples were obtained from eight patients (eight periodontal pockets) before and 1 week after the local drug delivery of minocycline. Although the number of P. gingivalis, P. intermedia and A. actinomycetemcomitans markedly decreased after the antibiotic therapy in most cases, higher copy numbers of the tetQ gene were detectable. The real-time PCR demonstrated sufficient sensitivity, specificity and quantitativity to be a powerful tool for microbiological examination in periodontal disease, and the quantitative monitoring of antibiotic resistance gene accompanied with the antibiotic therapy should be included in the examination.

Original languageEnglish
Pages (from-to)81-86
Number of pages6
JournalFEMS Immunology and Medical Microbiology
Volume39
Issue number1
DOIs
Publication statusPublished - Oct 24 2003

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Prevotella intermedia
Aggregatibacter actinomycetemcomitans
Porphyromonas gingivalis
Real-Time Polymerase Chain Reaction
Bacteria
Periodontal Diseases
Microbial Drug Resistance
Sensitivity and Specificity
Genes
Coloring Agents
Fluorescence
16S Ribosomal RNA
Anti-Bacterial Agents
Periodontal Pocket
Tetracycline Resistance
Dental Plaque
Minocycline
Gene Dosage
rRNA Genes
Therapeutics

Keywords

  • 16S rRNA gene
  • Periodontal bacterium
  • Real-time PCR
  • SYBR Green
  • TaqMan
  • TetQ gene

ASJC Scopus subject areas

  • Immunology
  • Microbiology
  • Infectious Diseases

Cite this

Quantitative real-time PCR using TaqMan and SYBR Green for Actinobacillus actinomycetemcomitans, Porphyromonas gingivalis, Prevotella intermedia, tetQ gene and total bacteria. / Maeda, Hiroshi; Fujimoto, Chiyo; Haruki, Yasuhiro; Maeda, Takemasa; Kokeguchi, Susumu; Petelin, Millan; Arai, Hideo; Tanimoto, Ichiro; Nishimura, Fusanori; Takashiba, Shogo.

In: FEMS Immunology and Medical Microbiology, Vol. 39, No. 1, 24.10.2003, p. 81-86.

Research output: Contribution to journalArticle

Maeda, Hiroshi ; Fujimoto, Chiyo ; Haruki, Yasuhiro ; Maeda, Takemasa ; Kokeguchi, Susumu ; Petelin, Millan ; Arai, Hideo ; Tanimoto, Ichiro ; Nishimura, Fusanori ; Takashiba, Shogo. / Quantitative real-time PCR using TaqMan and SYBR Green for Actinobacillus actinomycetemcomitans, Porphyromonas gingivalis, Prevotella intermedia, tetQ gene and total bacteria. In: FEMS Immunology and Medical Microbiology. 2003 ; Vol. 39, No. 1. pp. 81-86.
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