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Subgingival microbiota from Cebus apella (capuchin monkey) with different periodontal conditions
Authors:Gaetti-Jardim Elerson  Monti Lira Marcela  Nicolas Ciesielski Francisco Isaak  Gaetti-Jardim Ellen Cristina  Okamoto Ana Cláudia  Schweitzer Christiane Marie  Avila-Campos Mario Julio
Affiliation:1. Department of Pathology and Oral Diagnostics, School of Dentistry, UNESP Univ Estadual Paulista, Rua José Bonifácio 1193, 16015-050 Araçatuba, SP, Brazil;2. Department of Mathematic, Engineering Faculty of Ilha Solteira, UNESP Univ Estadual Paulista, Alameda Rio de Janeiro 266, 15385-000 Ilha Solteira, SP, Brazil;3. Anaerobe Laboratory, Department of Microbiology, Institute of Biomedical Sciences, University of São Paulo-USP, Av. Lineu Prestes, 2415-242 São Paulo, SP, Brazil;1. Oral Health Science Center, Tokyo Dental College, 2-1-14 Kanda-Misakicho, Chiyoda-ku, Tokyo, 101-0061, Japan;2. Department of Microbiology, Tokyo Dental College, 2-1-14 Kanda-Misakicho, Chiyoda-ku, Tokyo, 101-0061, Japan;1. Clinic of Digestive and Endocrine Surgery, Hôtel-Dieu, University Hospital of Nantes, Nantes, France;2. Department of Anesthesiology and Surgical Intensive Care, Hôtel-Dieu, University Hospital of Nantes, Nantes, France
Abstract:This present study evaluated the subgingival microbiota of the Cebus apella with different periodontal conditions kept by the Tufted Capuchin Monkey Procreation Center (São PauloState University – UNESP) or free-ranging monkeys. For this purpose, clinical specimens of subgingival biofilm were collected from 52 monkeys, of both genders, 40 kept in captivity and 12 free-ranging monkeys. The primates were submitted to periodontal evaluation and biofilm samples were transferred to VMGA III transport medium and ultrapure water. The microbiota was cultivated in selective and non-selective culture media and microbial DNA was extracted and the presence of periodontal pathogens was evaluated using PCR and real-time PCR. The actinomycetes, fusobacteria, Campylobacter rectus, Eikenella corrodens, black-pigmented Gram-negative anaerobic rods, Tannerella forsythia, staphylococci and streptococci represent the predominantly detected microorganisms. Aggregatibacter actinomycetemcomitans, Dialister pneumosintes and Prevotella nigrescens were rarely observed, whereas Treponema denticola was not found. Populations of C. rectus, E. corrodens, Fusobacterium nucleatum, Porphyromonas gingivalis, Prevotella intermedia, T. forsythia and the total microbial load were significantly higher in animals with bone loss and, in smaller extension, in animals with gingival bleeding.
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