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Multiplex Antimicrobial Activities of the Self-assembled Amphiphilic Polypeptide β Nanofiber KF-5 Against Vaginal Pathogens

Overview
Journal Biol Direct
Publisher Biomed Central
Specialty Biology
Date 2024 Oct 23
PMID 39438996
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Abstract

Background: Vaginal infections caused by multidrug-resistant pathogens such as Candida albicans and Gardnerella spp. represent a significant health challenge. Current treatments often fail because of resistance and toxicity. This study aimed to synthesize and characterize a novel amphiphilic polypeptide, KF-5, and evaluate its antibacterial and antifungal activities, biocompatibility, and potential mechanisms of action.

Results: The KF-5 peptide was synthesized via solid-phase peptide synthesis and self-assembled into nanostructures with filamentous and hydrogel-like configurations. Characterization by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and atomic force microscopy (AFM) confirmed the unique nanostructural properties of KF-5. KF-5 (125, 250, or 500 µg/ml) demonstrated potent antibacterial and antifungal activities, with significant inhibitory effects on drug-resistant Candida albicans and Gardnerella spp. (P < 0.05). In vitro assays revealed that 500 µg/ml KF-5 disrupted microbial cell membranes, increased membrane permeability, and induced lipid oxidation, leading to cell death (P < 0.05). Cytotoxicity tests revealed minimal toxicity in human vaginal epithelial cells, keratinocytes, and macrophages, with over 95% viability at high concentrations. Molecular dynamics simulations indicated that KF-5 interacts with phospholipid bilayers through electrostatic interactions, causing membrane disruption. In vivo studies using a mouse model of vaginal infection revealed that 0.5, 1, and 2 mg/ml KF-5 significantly reduced fungal burden and inflammation, and histological analysis confirmed the restoration of vaginal mucosal integrity (P < 0.01). Compared with conventional antifungal treatments such as miconazole, KF-5 exhibited superior efficacy (P < 0.01).

Conclusions: KF-5 demonstrates significant potential as a safe and effective antimicrobial agent for treating vaginal infections. Its ability to disrupt microbial membranes while maintaining biocompatibility with human cells highlights its potential for clinical application. These findings provide a foundation for further development of KF-5 as a therapeutic option for combating drug-resistant infections.

References
1.
Xie Y, Qin X, Zhang J, Sun M, Wang F, Huang M . Self-assembly of peptide nanofibers with chirality-encoded antimicrobial activity. J Colloid Interface Sci. 2022; 622:135-146. DOI: 10.1016/j.jcis.2022.04.058. View

2.
Zhang H, Wei W, Zhao M, Ma L, Jiang X, Pei H . Interaction between Aβ and Tau in the Pathogenesis of Alzheimer's Disease. Int J Biol Sci. 2021; 17(9):2181-2192. PMC: 8241728. DOI: 10.7150/ijbs.57078. View

3.
Tomas M, Palmeira-de-Oliveira A, Simoes S, Martinez-de-Oliveira J, Palmeira-de-Oliveira R . Bacterial vaginosis: Standard treatments and alternative strategies. Int J Pharm. 2020; 587:119659. DOI: 10.1016/j.ijpharm.2020.119659. View

4.
Diez-Pascual A, Rahdar A . Functional Nanomaterials in Biomedicine: Current Uses and Potential Applications. ChemMedChem. 2022; 17(16):e202200142. PMC: 9544115. DOI: 10.1002/cmdc.202200142. View

5.
Chen D, Liu X, Chen Y, Lin H . Amyloid peptides with antimicrobial and/or microbial agglutination activity. Appl Microbiol Biotechnol. 2022; 106(23):7711-7720. PMC: 9628408. DOI: 10.1007/s00253-022-12246-w. View