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Antifungal effects of synthetic human β-defensin 3-C15 peptide
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 β-defensin 3 (HBD3-C15) with calcium hydroxide (CH) and Nystatin (Nys) against Candida albicans (C. albicans) biofilm. MATERIALS AND MET...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Academy of Conservative Dentistry
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4868883/ https://www.ncbi.nlm.nih.gov/pubmed/27200276 http://dx.doi.org/10.5395/rde.2016.41.2.91 |
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author | 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 |
author_facet | 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 |
author_sort | Lim, Sang-Min |
collection | PubMed |
description | 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 β-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 µg/mL), CH (100 µg/mL), and Nys (20 µg/mL) for 7 days at 37℃. 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 (≥ 100 µg/mL). CLSM showed C. albicans survival was reduced by HBD3-C15 in a dose dependent manner. Nys and HBD3-C15 (≥ 100 µg/mL) showed significant fungicidal activity compared to CH group (p < 0.05). CONCLUSIONS: Synthetic HBD3-C15 peptide (≥ 100 µg/mL) and Nys exhibited significantly higher antifungal activity than CH against C. albicans by inhibiting cell survival and biofilm. |
format | Online Article Text |
id | pubmed-4868883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Korean Academy of Conservative Dentistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-48688832016-05-19 Antifungal effects of synthetic human β-defensin 3-C15 peptide 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 Restor Dent Endod Research Article 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 β-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 µg/mL), CH (100 µg/mL), and Nys (20 µg/mL) for 7 days at 37℃. 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 (≥ 100 µg/mL). CLSM showed C. albicans survival was reduced by HBD3-C15 in a dose dependent manner. Nys and HBD3-C15 (≥ 100 µg/mL) showed significant fungicidal activity compared to CH group (p < 0.05). CONCLUSIONS: Synthetic HBD3-C15 peptide (≥ 100 µg/mL) and Nys exhibited significantly higher antifungal activity than CH against C. albicans by inhibiting cell survival and biofilm. The Korean Academy of Conservative Dentistry 2016-05 2016-03-17 /pmc/articles/PMC4868883/ /pubmed/27200276 http://dx.doi.org/10.5395/rde.2016.41.2.91 Text en ©Copyrights 2016. The Korean Academy of Conservative Dentistry. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article 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 Antifungal effects of synthetic human β-defensin 3-C15 peptide |
title | Antifungal effects of synthetic human β-defensin 3-C15 peptide |
title_full | Antifungal effects of synthetic human β-defensin 3-C15 peptide |
title_fullStr | Antifungal effects of synthetic human β-defensin 3-C15 peptide |
title_full_unstemmed | Antifungal effects of synthetic human β-defensin 3-C15 peptide |
title_short | Antifungal effects of synthetic human β-defensin 3-C15 peptide |
title_sort | antifungal effects of synthetic human β-defensin 3-c15 peptide |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4868883/ https://www.ncbi.nlm.nih.gov/pubmed/27200276 http://dx.doi.org/10.5395/rde.2016.41.2.91 |
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