Candidacidal and Antibiofilm Activity of PS1-3 Peptide against Drug-Resistant <i>Candida albicans</i> on Contact Lenses

The recent emergence of antibiotic-resistant fungi has accelerated research on novel antifungal agents. In particular, <i>Candida albicans</i> infections are related to biofilm formation on medical devices, such as catheters, stents, and contact lenses, resulting in high morbidity and mo...

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Main Authors: Jong-Kook Lee, Soyoung Park, Young-Min Kim, Taeuk Guk, Min-Young Lee, Seong-Cheol Park, Jung Ro Lee, Mi-Kyeong Jang
Format: Article
Language:English
Published: MDPI AG 2022-07-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/14/8/1602
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author Jong-Kook Lee
Soyoung Park
Young-Min Kim
Taeuk Guk
Min-Young Lee
Seong-Cheol Park
Jung Ro Lee
Mi-Kyeong Jang
author_facet Jong-Kook Lee
Soyoung Park
Young-Min Kim
Taeuk Guk
Min-Young Lee
Seong-Cheol Park
Jung Ro Lee
Mi-Kyeong Jang
author_sort Jong-Kook Lee
collection DOAJ
description The recent emergence of antibiotic-resistant fungi has accelerated research on novel antifungal agents. In particular, <i>Candida albicans</i> infections are related to biofilm formation on medical devices, such as catheters, stents, and contact lenses, resulting in high morbidity and mortality. In this study, we aimed to elucidate the antifungal and antibiofilm effects of a peptide against drug-resistant <i>C. albicans</i>. α-Helical peptides in which the sequence of KWYK was repeated twice and four times, designated peptide series 1 (PS1)-1 and PS1-3, respectively, were generated, and the candidacidal activities of PS1-1, PS1-3, and fluconazole against drug-resistant <i>C. albicans</i> cells were assessed. The PS1-3 peptide showed higher killing activity than PS1-1 or fluconazole and acted via a membranolytic mechanism. In addition, the PS1-3 peptide exhibited more potent activity than PS1-1 and fluconazole in terms of fungal biofilm inhibition and reduction at the minimum fungicidal concentration on the contact lens surface. Overall, these findings established PS1-3 as a potential candidacidal agent for applications on contact lenses.
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spelling doaj.art-828b74fb5811438db0150f051a25cc382023-12-03T14:17:12ZengMDPI AGPharmaceutics1999-49232022-07-01148160210.3390/pharmaceutics14081602Candidacidal and Antibiofilm Activity of PS1-3 Peptide against Drug-Resistant <i>Candida albicans</i> on Contact LensesJong-Kook Lee0Soyoung Park1Young-Min Kim2Taeuk Guk3Min-Young Lee4Seong-Cheol Park5Jung Ro Lee6Mi-Kyeong Jang7Department of Chemical Engineering, Sunchon National University, Suncheon 57922, KoreaDepartment of Chemical Engineering, Sunchon National University, Suncheon 57922, KoreaDepartment of Chemical Engineering, Sunchon National University, Suncheon 57922, KoreaDepartment of Chemical Engineering, Sunchon National University, Suncheon 57922, KoreaDepartment of Clinical Laboratory Science, Daejeon Health Institute of Technology, Daejeon 34504, KoreaDepartment of Chemical Engineering, Sunchon National University, Suncheon 57922, KoreaLMO Team, National Institute of Ecology (NIE), Seocheon 33657, KoreaDepartment of Chemical Engineering, Sunchon National University, Suncheon 57922, KoreaThe recent emergence of antibiotic-resistant fungi has accelerated research on novel antifungal agents. In particular, <i>Candida albicans</i> infections are related to biofilm formation on medical devices, such as catheters, stents, and contact lenses, resulting in high morbidity and mortality. In this study, we aimed to elucidate the antifungal and antibiofilm effects of a peptide against drug-resistant <i>C. albicans</i>. α-Helical peptides in which the sequence of KWYK was repeated twice and four times, designated peptide series 1 (PS1)-1 and PS1-3, respectively, were generated, and the candidacidal activities of PS1-1, PS1-3, and fluconazole against drug-resistant <i>C. albicans</i> cells were assessed. The PS1-3 peptide showed higher killing activity than PS1-1 or fluconazole and acted via a membranolytic mechanism. In addition, the PS1-3 peptide exhibited more potent activity than PS1-1 and fluconazole in terms of fungal biofilm inhibition and reduction at the minimum fungicidal concentration on the contact lens surface. Overall, these findings established PS1-3 as a potential candidacidal agent for applications on contact lenses.https://www.mdpi.com/1999-4923/14/8/1602antifungal activityantimicrobial peptidecandidacidal activitybiofilm
spellingShingle Jong-Kook Lee
Soyoung Park
Young-Min Kim
Taeuk Guk
Min-Young Lee
Seong-Cheol Park
Jung Ro Lee
Mi-Kyeong Jang
Candidacidal and Antibiofilm Activity of PS1-3 Peptide against Drug-Resistant <i>Candida albicans</i> on Contact Lenses
Pharmaceutics
antifungal activity
antimicrobial peptide
candidacidal activity
biofilm
title Candidacidal and Antibiofilm Activity of PS1-3 Peptide against Drug-Resistant <i>Candida albicans</i> on Contact Lenses
title_full Candidacidal and Antibiofilm Activity of PS1-3 Peptide against Drug-Resistant <i>Candida albicans</i> on Contact Lenses
title_fullStr Candidacidal and Antibiofilm Activity of PS1-3 Peptide against Drug-Resistant <i>Candida albicans</i> on Contact Lenses
title_full_unstemmed Candidacidal and Antibiofilm Activity of PS1-3 Peptide against Drug-Resistant <i>Candida albicans</i> on Contact Lenses
title_short Candidacidal and Antibiofilm Activity of PS1-3 Peptide against Drug-Resistant <i>Candida albicans</i> on Contact Lenses
title_sort candidacidal and antibiofilm activity of ps1 3 peptide against drug resistant i candida albicans i on contact lenses
topic antifungal activity
antimicrobial peptide
candidacidal activity
biofilm
url https://www.mdpi.com/1999-4923/14/8/1602
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