Antifungal Activity and Action Mechanism of Histatin 5-Halocidin Hybrid Peptides against Candida ssp
- Authors
- Han, Juhye; Jyoti, Md. Anirban; Song, Ho-Yeon; Jang, Woong Sik
- Issue Date
- 26-Feb-2016
- Publisher
- Public Library of Science
- Keywords
- Antifungal Activity; Histatin 5-Halocidin Hybrid peptides; Candida ssp
- Citation
- PLoS ONE, v.11, no.2
- Journal Title
- PLoS ONE
- Volume
- 11
- Number
- 2
- URI
- https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/9346
- DOI
- 10.1371/journal.pone.0150196
- ISSN
- 1932-6203
- Abstract
- The candidacidal activity of histatin 5 is initiated through cell wall binding, followed by translocation and intracellular targeting, while the halocidin peptide exerts its activity by attacking the Candida cell membrane. To improve antimicrobial activities and to understand the killing mechanism of two peptides, six hybrid peptides were designed by conjugating histatin 5 and halocidin. A comparative approach was established to study the activity, salt tolerance, cell wall glucan binding assay, cytotoxicity, generation of ROS and killing kinetics. CD spectrometry was conducted to evaluate secondary structures of these hybrid peptides. Furthermore the cellular localization of hybrid peptides was investigated by confocal fluorescence microscopy. Of the six hybrid congeners, di-PH2, di-WP2 and HHP1 had stronger activities than other hybrid peptides against all tested Candida strains. The MIC values of these peptides were 1-2, 2-4 and 2-4 mu g/ml, respectively. Moreover, none of the hybrid peptides was cytotoxic in the hemolytic assay and cell-based cytotoxicity assay. Confocal laser microscopy showed that di-PH2 and HHP1 were translocated into cytoplasm whereas di-WP2 was accumulated on surface of C. albicans to exert their candidacidal activity. All translocated peptides (Hst 5, P113, di-PH2) were capable of generating intracellular ROS except HHP1. Additionally, the KFH residues at C-terminal end of these peptides were assumed for core sequence for active translocation.
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