Abstract

This study investigated the effects of Brazilian Red Propolis (BRP) extract on seven-day-old multispecies subgingival biofilms. Mixed biofilm cultures containing 31 species associated with periodontal health or disease were grown for six days on a Calgary device. Then, mature biofilms were treated for 24 h with BRP extract at different concentrations (200–1600 µg/mL), amoxicillin (AMOXI) at 54 µg/mL (positive control) or vehicle (negative control). Biofilm metabolic activity was determined by colorimetry, and bacterial counts/proportions were determined by DNA–DNA hybridization. Data were analyzed by Kruskal–Wallis and Dunn’s tests. Treatment with BRP at 1600, 800 and 400 μg/mL reduced biofilm metabolic activity by 56%, 56% and 57%, respectively, as compared to 65% reduction obtained with AMOXI. Mean total cell counts were significantly reduced in all test groups (~50–55%). Lower proportions of red, green and yellow complex species were observed upon treatment with BRP (400 µg/mL) and AMOXI, but only AMOXI reduced the proportions of Actinomyces species. In conclusion, BRP extract was as effective as AMOXI in killing seven-day-old multispecies biofilm pathogens and did not affect the levels of the host-compatible Actinomyces species. These data suggest that BRP may be an alternative to AMOXI as an adjunct in periodontal therapy. In vivo studies are needed to validate these results.

Highlights

  • The main etiological factor of periodontal disease is a dysbiosis of the oral subgingival biofilm associated with the presence of periodontopathogens, mainly Porphyromonas gingivalis, Tannerella forsythia, Treponema denticola and Aggregatibacter actinomycetemcomitans

  • Our study showed that Brazilian Red Propolis (BRP) extract was effective in reducing the metabolic activity and total cell counts of red-complex in mature to AMOXI

  • The red complex is composed by microorganisms associated with disease; the orange complex is associated with the health–disease transition, while the yellow, purple and green complexes as well as Actinomyces species are associated with a healthy periodontal condition [23]

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Summary

Introduction

The main etiological factor of periodontal disease is a dysbiosis of the oral subgingival biofilm associated with the presence of periodontopathogens, mainly Porphyromonas gingivalis, Tannerella forsythia, Treponema denticola and Aggregatibacter actinomycetemcomitans. These microorganisms release metabolic byproducts or components (e.g., lipopolysaccharides and fimbriae) into periodontal tissues, causing an exacerbated inflammatory response which leads to tissue destruction [1]. The treatment of periodontal diseases consists of controlling the occurrence of periodontopathogenic microorganisms to reduce or eliminate tissue inflammation. Mechanical removal of subgingival biofilms by means of scaling and root planning (SRP) significantly improves all periodontal clinical parameters. The mechanical therapy alone may not be fully effective to reverse the major

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