Microbial analysis of canals of root-filled teeth with periapical lesions using polymerase chain reaction

被引:154
作者
Gomes, Brenda P. F. A. [1 ]
Pinheiro, Ericka T. [1 ]
Jacinto, Rogerio C. [1 ]
Zaia, Alexandre A. [1 ]
Ferraz, Caio C. R. [1 ]
Souza-Filbo, Francisco J. [1 ]
机构
[1] Univ Estadual Campinas, UNICAMP, Dept Restorat Dent, Endodont Div,Piracicaba Dent Sch, Piracicaba, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
bacteria; endodontic failure; polymerase chain reaction;
D O I
10.1016/j.joen.2008.01.016
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
The objective of the present study was to investigate the presence of nine bacterial species in root-filled teeth associated with periapical lesions using a polymerase chain reaction analysis and to correlate these species with clinical features of the cases. DNA was extracted from 45 canal samples of root-filled teeth with periapical lesions. A PCR assay using species-specific primers of 16S rDNA and the downstream intergenic spacer region was used for microbial detection. Enterococcus faecalis was the most prevalent species, detected in 77.8% of the study teeth, followed by Peptostreptococcus micros, detected in 51.1%. Porphyromonas gingivalis, Porphyromonas endodontalis, Prevotella intermedia, and Prevotella nigrescens were detected in 35.6%, 22.2%, 11.1%, and 11.1% of the sampled teeth, respectively. Moreover, PCR detected Filifactor alocis in 26.7%, Treponema denticola in 24.4%, and Tannerella forsythia in 4.4% of the samples. T. denticola and P. micros were statistically associated with tenderness to percussion (p < 0.05). P. nigrescens was associated with the presence of spontaneous pain and abscess (p < 0.05). P. endodontalis and P. nigrescens were associated with purulent exudates (p < 0.05). Synergistic relationship was also observed between some species. The results of this study indicated that E. faecalis was the most frequently identified test species by PCR in teeth with failing endodontic treatment.
引用
收藏
页码:537 / 540
页数:4
相关论文
共 28 条
[1]   Geographical differences in bacteria detected in endodontic infections using polymerase chain reaction [J].
Baumgartner, JC ;
Siqueira, JF ;
Xia, T ;
Rôças, IN .
JOURNAL OF ENDODONTICS, 2004, 30 (03) :141-144
[2]   Microbial flora of root canal-treated teeth associated with asymptomatic periapical radiolucent lesions [J].
Cheung, GSP ;
Ho, MWM .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 2001, 16 (06) :332-337
[3]   A COMPARISON OF 2 TRANSPORT MEDIA FOR SALIVA AND SUBGINGIVAL SAMPLES [J].
DAHLEN, G ;
PIPATTANAGOVIT, P ;
ROSLING, B ;
MOLLER, AJR .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 1993, 8 (06) :375-382
[4]   An in vitro comparison of the antimicrobial effects of various endodontic medicaments on Enterococcus faecalis [J].
Davis, Joshua M. ;
Maki, James ;
Bahcall, James K. .
JOURNAL OF ENDODONTICS, 2007, 33 (05) :567-569
[5]   Molecular detection of Enterococcus species in root canals of therapy-resistant endodontic infections [J].
Fouad, AF ;
Zerella, J ;
Barry, J ;
Spångberg, LS .
ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTOLOGY, 2005, 99 (01) :112-118
[6]  
GOMES BPF, 2004, J DENT RES, V83, DOI UNSP 1040SL
[7]   Porphyromonas gingivalis, Porphyromonas endodontalis, Prevotella intermedia and Prevotella nigrescens in endodontic lesions detected by culture and by PCR [J].
Gomes, BPFA ;
Jacinto, RC ;
Pinheiro, ET ;
Sousa, ELR ;
Zaia, AA ;
Ferraz, CCR ;
Souza, FJ .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 2005, 20 (04) :211-215
[8]   Bacteria isolated after unsuccessful endodontic treatment in a North American population [J].
Hancock, HH ;
Sigurdsson, A ;
Trope, M ;
Moiseiwitsch, J .
ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTICS, 2001, 91 (05) :579-586
[9]   Enterococcus spp. in endodontically treated teeth with and without periradicular lesions [J].
Kaufman, B ;
Spångberg, L ;
Barry, J ;
Fouad, AF .
JOURNAL OF ENDODONTICS, 2005, 31 (12) :851-856
[10]   Development of a PCR assay for rapid detection of enterococci [J].
Ke, DB ;
Picard, FJ ;
Martineau, F ;
Ménard, C ;
Roy, PH ;
Ouellette, M ;
Bergeron, MG .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (11) :3497-3503