Molecular analyses of two bacterial sampling methods in ligature-induced periodontitis in rats

The prevalence profile of periodontal pathogens in dental plaque can vary as a function of the detection method; however, the sampling technique may also play a role in determining dental plaque microbial profiles. We sought to determine the bacterial composition comparing two sampling methods, one...

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Bibliographic Details
Authors: Fontana, Carla Raquel [UNESP], Grecco, Clovis, Bagnato, Vanderlei Salvador, de Freitas, Laura Marise [UNESP], Boussios, Constantinos I., Soukos, Nikolaos S.
Format: article
Status:Published version
Publication Date:2018
Country:Brasil
Institution:Universidade Estadual Paulista (UNESP)
Repository:Repositório Institucional da UNESP
Language:English
OAI Identifier:oai:repositorio.unesp.br:11449/170677
Online Access:http://dx.doi.org/10.1002/cre2.98
http://hdl.handle.net/11449/170677
Access Level:Open access
Keyword:biofilm, periodontal pathogens
molecular diagnostics
sampling technique
Description
Summary:The prevalence profile of periodontal pathogens in dental plaque can vary as a function of the detection method; however, the sampling technique may also play a role in determining dental plaque microbial profiles. We sought to determine the bacterial composition comparing two sampling methods, one well stablished and a new one proposed here. In this study, a ligature-induced periodontitis model was used in 30 rats. Twenty-seven days later, ligatures were removed and microbiological samples were obtained directly from the ligatures as well as from the periodontal pockets using absorbent paper points. Microbial analysis was performed using DNA probes to a panel of 40 periodontal species in the checkerboard assay. The bacterial composition patterns were similar for both sampling methods. However, detection levels for all species were markedly higher for ligatures compared with paper points. Ligature samples provided more bacterial counts than paper points, suggesting that the technique for induction of periodontitis could also be applied for sampling in rats. Our findings may be helpful in designing studies of induced periodontal disease-associated microbiota.