Enumeration of Porphyromonas gingivalis, Prevotella intermedia and Actinobacillus actinomycetemcomitans in subgingival plaque samples by a quantitative-competitive PCR method

被引:47
作者
Doungudomdacha, S
Rawlinson, A
Douglas, CWI [1 ]
机构
[1] Univ Sheffield, Sch Clin Dent, Dept Oral Pathol, Sheffield S10 2TA, S Yorkshire, England
[2] Univ Sheffield, Sch Clin Dent, Dept Restorat Dent, Sheffield S10 2TA, S Yorkshire, England
关键词
D O I
10.1099/0022-1317-49-10-861
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Porphyromonas gingivalis, Prevotella intermedia and Actinobacillus actinomycetemcomitans are believed to play an important role in adult periodontitis, but the significance of their relative numbers and progress of the disease is still unclear. Traditional quantitative methods are generally time-consuming and inaccurate, The aim of this study was to develop a sensitive, quantitative PCR technique that would be useful for enumerating P. gingivalis, Pr. intermedia and A, actinomycetemcomitans in subgingival plaque samples from subjects with adult periodontitis. Primers to the following genes were employed: the fimbrial gene (fimA) of P. gingivalis, the 16S rRNA gene of Pr. intermedia and the leukotoxin-A (lktA) gene of A. actinomycetemcomitans. Competitive templates were constructed either by sequence deletion between primer binding sites or by annealing of the primer binding sites to an appropriate DNA core so as to yield products of a different size from that obtained with the target template. Coamplification of target and competitive templates yielded products of expected size and non-specific recognition by the primers was not found. The sensitivity of the designed primers was 100 cells of P. gingivalis, 100 cells of Pr. intermedia and 10 cells of A. actinomycetemcomitans. The three species were found in subgingival plaque samples collected from both healthy and diseased sites by the quantitative-competitive (QC)-PCR method and the technique was more sensitive than cultural methods. For determining the proportions of each of the three periodontopathogens, the total number of bacteria in the samples was enumerated by quantitative-PCR with 16S rRNA universal primers (27f and 342r). The findings indicate that QC-PCR is a useful method for enumerating bacteria in clinical oral specimens and the technique could play a role in the investigation of disease progression.
引用
收藏
页码:861 / 874
页数:14
相关论文
共 44 条
[1]   PCR AMPLIFICATION OF HIGHLY GC-RICH DNA-TEMPLATE AFTER DENATURATION BY NAOH [J].
AGARWAL, RK ;
PERL, A .
NUCLEIC ACIDS RESEARCH, 1993, 21 (22) :5283-5284
[2]   Structural domains of Porphyromonas gingivalis recombinant fimbrillin that mediate binding to salivary proline-rich protein and statherin [J].
Amano, A ;
Sharma, A ;
Lee, JY ;
Sojar, HT ;
Raj, PA ;
Genco, RJ .
INFECTION AND IMMUNITY, 1996, 64 (05) :1631-1637
[3]   Polymerase chain reaction detection of 8 putative periodontal pathogens in subgingival plaque of gingivitis and advanced periodontitis lesions [J].
Ashimoto, A ;
Chen, C ;
Bakker, I ;
Slots, J .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 1996, 11 (04) :266-273
[4]   Uniform amplification of a mixture of deoxyribonucleic acids with varying GC content [J].
Baskaran, N ;
Kandpal, RP ;
Bhargava, AK ;
Glynn, MW ;
Bale, A ;
Weissman, SM .
GENOME RESEARCH, 1996, 6 (07) :633-638
[5]  
CHRISTERSSON LA, 1989, J DENT RES, V68, P1633
[6]   QUANTITATIVE PCR - VALIDATION OF THE USE OF A MULTISPECIFIC INTERNAL CONTROL [J].
COTTREZ, F ;
AURIAULT, C ;
CAPRON, A ;
GROUX, H .
NUCLEIC ACIDS RESEARCH, 1994, 22 (13) :2712-2713
[7]  
Dahlen G, 1993, Adv Dent Res, V7, P163
[8]   Comparison of the ABI 7700 system (TaqMan) and competitive PCR for quantification of IS6110 DNA in sputum during treatment of tuberculosis [J].
Desjardin, LE ;
Chen, Y ;
Perkins, MD ;
Teixeira, L ;
Cave, MD ;
Eisenach, KD .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (07) :1964-1968
[9]   GENERAL-METHOD FOR AMPLIFYING REGIONS OF VERY HIGH G-PLUS-C CONTENT [J].
DUTTON, CM ;
PAYNTON, C ;
SOMMER, SS .
NUCLEIC ACIDS RESEARCH, 1993, 21 (12) :2953-2954
[10]   COLORIMETRIC MICROTITER PLATE BASED ASSAY FOR DETECTION AND QUANTIFICATION OF AMPLIFIED ACTINOBACILLUS-ACTINOMYCETEMCOMITANS DNA [J].
FUJISE, O ;
HAMACHI, T ;
HIROFUJI, T ;
MAEDA, K .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 1995, 10 (06) :372-377