Abstract

Periodontopathogenic subgingival biofilm is the main etiological agent of periodontitis. Thus, a search for antimicrobials as adjuvant for periodontal treatment in the literature is intense. Cetylpyridinium chloride (CPC) is a well-known antimicrobial agent commonly used in mouthrinses. However, CPC effects on a complex biofilm model were not found over the literature. Therefore, the aim of this manuscript is to evaluate 0.075% CPC antimicrobial properties in a multispecies subgingival biofilm model in vitro. The subgingival biofilm composed by 31 species related to periodontitis was formed for 7 days, using the calgary device. The treatments with CPC and chlorhexidine (CHX) 0.12% (as positive control) were performed 2x/day, for 1 min, from day 3 until the end of experimental period, totaling 8 treatments. After 7 days of biofilm formation, biofilm metabolic activity was evaluated by a colorimetric reaction and biofilms microbial composition by DNA-DNA hybridization. Statistical analysis was performed using ANOVA with data transformed via BOX-COX followed by Dunnett post-hoc. Both CPC and CHX reduced biofilm metabolic activity in 60% and presented antimicrobial activity against 13 different species. Specifically, only CHX reduced levels of F.n. vicentii and P. gingivalis while only CPC reduced A. odontolyticus and A. israelli. CPC was as effective as CHX as antimicrobial through in vitro complex multispecies subgingival biofilm. However, future studies using in vivo models of experimental periodontal disease should be performed to prove such effect.

Highlights

  • Periodontal diseases are mixed infections caused by bacterial species organized into a dysbiotic biofilm that colonize dental surfaces and induces a host inflammatory response, leading to destruction of tooth supporting tissues and tooth loss

  • After DNA attachment to the membrane, it was placed in Chlorhexidine is commonly used as adjuvant to a Miniblotter 45 (Immunetics)

  • Digoxigenin labeled with DNA probes of the entire genome for the subgingival species used were hybridized to individual lanes of Miniblotter 45

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Summary

Introduction

Periodontal diseases are mixed infections caused by bacterial species organized into a dysbiotic biofilm that colonize dental surfaces and induces a host inflammatory response, leading to destruction of tooth supporting tissues and tooth loss. The main etiological factor of periodontitis is the subgingival biofilm [1]. A classical manuscript of Socransky [2] identified the microbiota found over thousands of periodontal patients and organized the microorganisms into five complexes, according to health or disease. In this way, several antimicrobials have been tested to control subgingival biofilm and chlorhexidine (CHX) is considered the gold agent to control biofilms in oral cavity. Taste loss and oral mucosa burning sensation are the most common chlorhexidine undesirable effects [3]

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