The Porphyromonas gingivalis O antigen is required for inhibition of apoptosis in gingival epithelial cells following bacterial infection. (4th November 2015)

• Record Type: Journal Article
• Authors: Soto, C.; Bugueño, I.; Hoare, A.; Gonzalez, S.; Venegas, D.; Salinas, D.; Melgar‐Rodríguez, S.; Vernal, R.; Gamonal, J.; Quest, A. F. G.; Pérez‐Donoso, J. M.; Bravo, D.
• Is Part Of: Journal of periodontal research. Volume 51:Number 4(2016)
• Page Start: 518
• Page End: 528
• Publication Date: 2015-11-04
• Subjects: apoptosis -- gingival epithelial cells -- lipopolysaccharide -- O‐antigen -- Porphyromonas gingivalis; Periodontics -- Periodicals; 617.632
• DOI: 10.1111/jre.12331
• Languages: English
• ISSNs: 0022-3484

Abstract

Abstract : Background and Objective: Porphyromonas gingivalis infection induces apoptosis inhibition in gingival epithelial cells; however, it is not fully understood which bacterial effectors are involved in this process. The aim of this study is to evaluate whether the P. gingivalis lipopolysaccharide (LPS), specifically the O‐antigen region, affects adherence, invasion, viability and apoptosis of gingival epithelial cells. Material and Methods: Gingival epithelial cells (OKF6/TERT2 line) were infected by different freshly prepared P. gingivalis clinical isolates, obtained from subjects with chronic periodontitis (CP3 and CP4) and healthy individuals (H1 and H3). Periodontitis and healthy isolates show differences in O‐antigen production, as healthy isolates lack the O‐antigen region. In addition, cells were infected by a site‐specific mutant lacking the O‐antigen portion. After 24 h postinfection, cell proliferation, viability and apoptosis were evaluated by Trypan blue, MTS and annexin V assays, respectively. Bacterial invasion, adhesion and proliferation were measured by gentamicin/metronidazole protection assays. Finally, toll‐like receptor (TLR)2 and TLR4 mRNA expression was evaluated by quantitative reverse transcription–polymerase chain reaction. Statistical analysis was performed using ANOVA, Tukey's or Dunnett's tests ( p < 0.05). Results: At 24 h postinfection, strains lacking the O‐antigen region (healthy isolates and O‐antigen ligase‐deficient strain) were unable to increase proliferation and viability, or decrease apoptosis as compared with strains producing intact LPS (periodontitis isolates and reference strain). However, the presence of the O‐antigen neither contributed to changes in the ability of the bacteria to adhere to or invade cells, nor to intracellular survival. The presence of O‐antigen also increased the expression of TLR4 (nearly sixfold), which correlated with inhibition of apoptosis. Conclusion: The O‐antigen region of P. gingivalis LPS is required to increase gingival epithelial cell viability upon infection by bacteria and this increase is attributable to a reduction in apoptosis. Moreover, although bacterial internalization is required, the effects observed are not due to alterations in P. gingivalis adherence, invasion or intracellular survival. Interestingly, inhibition of apoptosis correlates with increased TLR4 expression, suggesting a role for TLR4 in this process.