Highbush blueberry proanthocyanidins alleviate Porphyromonas gingivalis-induced deleterious effects on oral mucosal cells

Anaerobe. 2020 Oct:65:102266. doi: 10.1016/j.anaerobe.2020.102266. Epub 2020 Aug 29.

Abstract

Strong evidence points to Porphyromonas gingivalis, a Gram-negative anaerobic bacterium, as a keystone species in the development of the chronic form of periodontitis. The aim of the present study was to investigate the ability of highbush blueberry proanthocyanidins (PACs) to alleviate the P. gingivalis-induced deleterious effects on oral mucosal cells. We first showed that highbush blueberry PACs protect the integrity of the gingival keratinocyte barrier against P. gingivalis-mediated damage, as determined by measuring the transepithelial electrical resistance and paracellular flux of FITC-conjugated dextran. Moreover, the PACs prevented the translocation of P. gingivalis across the gingival keratinocyte barrier model. The proteinase activity of P. gingivalis was inhibited by the PACs suggesting that they may exert beneficial effects by reducing proteolytic degradation of the epithelial tight junctions. Regulation of gingival fibroblast inflammatory reactions may be one of the ways to prevent and control periodontal disease progression and severity. We showed that PACs significantly reduce IL-6 and IL-8 secretion by P. gingivalis-stimulated gingival fibroblasts. The present study showed the capacity of highbush blueberry PACs to protect the integrity of an in vitro model of gingival keratinocyte barrier against P. gingivalis, and to attenuate the secretion of pro-inflammatory cytokines by gingival fibroblasts infected with P. gingivalis. These results suggest beneficial effects of blueberry PACs thus supporting the need for future clinical trials on the potential of these bioactive molecules for periodontal disease prevention and/or treatment.

MeSH terms

  • Bacteroidaceae Infections / drug therapy
  • Bacteroidaceae Infections / microbiology*
  • Blueberry Plants / chemistry*
  • Cells, Cultured
  • Cytokines / biosynthesis
  • Humans
  • Inflammation Mediators / metabolism
  • Keratinocytes / drug effects
  • Keratinocytes / metabolism
  • Keratinocytes / microbiology
  • Mouth Mucosa / microbiology
  • Mouth Mucosa / pathology
  • Periodontitis / drug therapy
  • Periodontitis / microbiology*
  • Periodontitis / pathology
  • Porphyromonas gingivalis / drug effects*
  • Proanthocyanidins / pharmacology*

Substances

  • Cytokines
  • Inflammation Mediators
  • Proanthocyanidins