Profiling of subgingival plaque biofilm microflora from periodontally healthy subjects and from subjects with periodontitis using quantitative real-time PCR

被引:96
作者
Abiko, Y. [1 ]
Sato, T. [1 ]
Mayanagi, G. [2 ]
Takahashi, N. [1 ]
机构
[1] Tohoku Univ, Grad Sch Dent, Div Oral Ecol & Biochem, Sendai, Miyagi 980, Japan
[2] Tohoku Univ, Grad Sch Dent, Div Periodontol & Endodontol, Sendai, Miyagi 980, Japan
关键词
16S ribosomal RNA; microflora; periodontitis; quantitative PCR; POLYMERASE-CHAIN-REACTION; ACID-NEUTRALIZING ACTIVITY; PORPHYROMONAS-GINGIVALIS; FUSOBACTERIUM-NUCLEATUM; PREVOTELLA-INTERMEDIA; PATHOGENS; BACTERIA; POCKETS; IDENTIFICATION; DISEASE;
D O I
10.1111/j.1600-0765.2009.01250.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background and Objective: Qualitative and quantitative changes of the subgingival plaque biofilm microflora in periodontal pockets are thought to be associated with the development and progression of periodontitis. The aims of the present study were to quantify the proportions of nine periodontitis-associated bacterial species and four Streptococcus species in subgingival plaque, and to evaluate their relationship with periodontitis quantitatively. Material and Methods: Subgingival plaque samples were obtained from 12 periodontally healthy subjects and from 28 patients with periodontitis. The amounts of total and target bacteria were measured by quantitative real-time PCR using universal and species-specific primers, respectively. Results: The proportion of total obligate anaerobes was found to be higher in subjects with periodontitis than in periodontally healthy subjects (p < 0.05). Among obligate anaerobes, Tannerella forsythia (2.04 +/- 5.27%, p < 0.05), Porphyromonas gingivalis (0.54 +/- 1.41%) and Eubacterium saphenum (0.30 +/- 0.96%) were detected at high proportions in subjects with periodontitis, but not in periodontally healthy subjects. By contrast, the proportion of total streptococci was lower in subjects with periodontitis (p < 0.05). Specifically, the proportion of T. forsythia, P. gingivalis or E. saphenum increased (>= 2.78%) and the proportion of Streptococcus species decreased to virtually undetectable levels, in subjects with periodontitis. Conclusion: Obligate anaerobes, including T. forthysia, P. gingivalis and E. saphenum, were identified predominantly in microflora from subjects with periodontitis, whereas Streptococcus species were identified predominantly in microflora from periodontally healthy subjects, suggesting a change in the subgingival environment that resulted in conditions more suitable for the survival of obligate anaerobes. The proportion of these obligate anaerobes in the subgingival plaque of subjects with periodontitis appears to be associated with the status of human periodontitis.
引用
收藏
页码:389 / 395
页数:7
相关论文
共 29 条
[1]   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
[2]   Gram-positive anaerobic bacilli in human periodontal disease [J].
Booth, V ;
Downes, J ;
Van den Berg, J ;
Wade, WG .
JOURNAL OF PERIODONTAL RESEARCH, 2004, 39 (04) :213-220
[3]   The additional value of real-time PCR in the quantitative detection of periodontal pathogens [J].
Boutaga, K ;
Van Winkelhoff, AJ ;
Vandenbroucke-Grauls, CMJE ;
Savelkoul, PHM .
JOURNAL OF CLINICAL PERIODONTOLOGY, 2006, 33 (06) :427-433
[4]   Subgingival microbiota in healthy, well-maintained elder and periodontitis subjects [J].
Haffajee, AD ;
Cugini, MA ;
Tanner, A ;
Pollack, RP ;
Smith, C ;
Kent, RL ;
Socransky, SS .
JOURNAL OF CLINICAL PERIODONTOLOGY, 1998, 25 (05) :346-353
[5]   Sampling of periodontal pathogens by paper points: evaluation of basic parameters [J].
Hartroth, B ;
Seyfahrt, I ;
Conrads, G .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 1999, 14 (05) :326-330
[6]   Detection of Slackia exigua, Mogibacterium timidum and Eubacterium saphenum from pulpal and periradicular samples using the Polymerase Chain Reaction (PCR) method [J].
Hashimura, T ;
Sato, M ;
Hoshino, E .
INTERNATIONAL ENDODONTIC JOURNAL, 2001, 34 (06) :463-470
[7]   PCR detection and identification of oral streptococci in saliva samples using gtf genes [J].
Hoshino, T ;
Kawaguchi, M ;
Shimizu, N ;
Hoshino, N ;
Ooshima, T ;
Fujiwara, T .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2004, 48 (03) :195-199
[8]   Quantitative detection of periodontal pathogens using real-time polymerase chain reaction with TaqMan probes [J].
Kuboniwa, M ;
Amano, A ;
Kimura, KR ;
Sekine, S ;
Kato, S ;
Yamamoto, Y ;
Okahashi, N ;
Iida, T ;
Shizukuishi, S .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 2004, 19 (03) :168-176
[9]  
Lane D J., 1991, Nucleic acid techniques in bacterial systematic, P115
[10]  
Lyons SR, 2000, J CLIN MICROBIOL, V38, P2362