Antifungal effects of synthetic human β-defensin 3-C15 peptide

• Published in: Restorative dentistry & endodontics Vol. 41; no. 2; pp. 91 - 97
• Main Authors: Lim, Sang-Min, Ahn, Ki-Bum, Kim, Christine, Kum, Jong-Won, Perinpanayagam, Hiran, Gu, Yu, Yoo, Yeon-Jee, Chang, Seok Woo, Han, Seung Hyun, Shon, Won-Jun, Lee, Woocheol, Baek, Seung-Ho, Zhu, Qiang, Kum, Kee-Yeon
• Format: Journal Article
• Language: Korean
• Published: 2016
• Subjects: Antifungal activity; albicans; C; LIVE/DEAD Biofilm viability assay; Human ${\beta}$-defensin-3 peptide; Confocal laser scanning microscopy; Dentin disk
• ISSN: 2234-7658; 2234-7666

Objectives: The purpose of this ex vivo study was to compare the antifungal activity of a synthetic peptide consisting of 15 amino acids at the C-terminus of human ${\beta}$-defensin 3 (HBD3-C15) with calcium hydroxide (CH) and Nystatin (Nys) against Candida albicans (C. albicans) biofilm. Materials and Methods: C. albicans were grown on cover glass bottom dishes or human dentin disks for 48 hr, and then treated with HBD3-C15 (0, 12.5, 25, 50, 100, 150, 200, and $300{\mu}g/mL$), CH ($100{\mu}g/mL$), and Nys ($20{\mu}g/mL$) for 7 days at $37^{\circ}C$. On cover glass, live and dead cells in the biomass were measured by the FilmTracer Biofilm viability assay, and observed by confocal laser scanning microscopy (CLSM). On dentin, normal, diminished and ruptured cells were observed by field-emission scanning electron microscopy (FE-SEM). The results were subjected to a two-tailed t-test, a one way analysis variance and a post hoc test at a significance level of p = 0.05. Results: C. albicans survival on dentin was inhibited by HBD3-C15 in a dose-dependent manner. There were fewer aggregations of C. albicans in the groups of Nys and HBD3-C15 (${\geq}100{\mu}g/mL$). CLSM showed C. albicans survival was reduced by HBD3-C15 in a dose dependent manner. Nys and HBD3-C15 (${\geq}100{\mu}g/mL$) showed significant fungicidal activity compared to CH group (p < 0.05). Conclusions: Synthetic HBD3-C15 peptide (${\geq}100{\mu}g/mL$) and Nys exhibited significantly higher antifungal activity than CH against C. albicans by inhibiting cell survival and biofilm.