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Identification of intracellular oral species within human crevicular epithelial cells from subjects with chronic periodontitis by fluorescence in situ hybridization
Author(s) -
Colombo A. V.,
Da Silva C. M.,
Haffajee A.,
Colombo A. P. V.
Publication year - 2007
Publication title -
journal of periodontal research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.31
H-Index - 83
eISSN - 1600-0765
pISSN - 0022-3484
DOI - 10.1111/j.1600-0765.2006.00938.x
Subject(s) - treponema denticola , tannerella forsythia , porphyromonas gingivalis , periodontitis , chronic periodontitis , buccal swab , microbiology and biotechnology , in situ hybridization , biology , buccal administration , bacteria , gingivitis , actinobacillus , pathology , medicine , dentistry , gene expression , gene , biochemistry , honeysuckle , genetics , alternative medicine , traditional chinese medicine
Background and Objective: Interactions between oral bacteria and gingival epithelial cells play an important role in the pathogenesis of periodontal diseases. This study used in situ hybridization with 16 rRNA probes and confocal microscopy to detect the periodontal pathogens Porphyromonas gingivalis , Actinobacillus actinomycetemcomitans , Tannerella forsythia , and Treponema denticola within epithelial cells from periodontal pockets, gingival crevice, and buccal mucosa collected from subjects with chronic periodontitis ( n = 14) and good periodontal health ( n = 8). Material and Methods: Each green fluorescent species‐specific and universal probe was hybridized with all 58 epithelial samples from the 22 patients. The samples were observed by confocal microscopy to confirm the intracellular localization of oral species of bacteria. The mean frequency of detection and number of intracellular bacteria per epithelial cell were computed for each sample. Results: The frequency of cells with internalized bacteria was higher in samples from the gingival crevice than in samples from the oral mucosa. Epithelial cells from all subjects harbored intracellular bacteria; however, patients with periodontitis presented significantly higher counts of bacteria per cell than periodontally healthy individuals ( p < 0.05). Periodontal pathogens showed a trend to be detected in higher numbers in epithelial cells from periodontitis patients. In particular, T. forsythia and T. denticola were significantly more prevalent in periodontal pocket cells than healthy sulci and buccal cell samples in the periodontitis group ( p < 0.05). Conclusion: Those findings indicate that crevicular and buccal cells present internalized bacteria, regardless of periodontal status. However, higher bacterial loads are detected in cells from subjects with periodontitis.