从人类乳铁蛋白中提取的合成肽 hLF(1-11) 与氟康唑/两性霉素 B 联合用于抗糠秕马拉色菌可产生协同/增效抗真菌效果。

IF 4.3 2区 医学 Q1 INFECTIOUS DISEASES Antibiotics-Basel Pub Date : 2024-08-22 DOI:10.3390/antibiotics13080790
Carlo P J M Brouwer, Bart Theelen, Youp van der Linden, Nick Sarink, Mahfuzur Rahman, Saleh Alwasel, Claudia Cafarchia, Mick M Welling, Teun Boekhout
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引用次数: 0

摘要

目的:马拉色菌酵母菌对常用抗真菌药物的耐药性不断增加,这就需要新型抗真菌化合物。以人类乳铁蛋白为基础的肽具有广谱的抗菌活性。为了找到酵母菌的最佳生长条件并评估细胞活力,我们采用了各种检测方法,并使用了低脂质含量的培养基,以避免肽与培养基成分结合:结果:hLF(1-11)抑制了所有受试菌株的生长,最低抑菌浓度(MIC)值从12.5到100 μg/mL不等。在联合试验中,大多数受试糠秕孢子菌菌株的分数抑制浓度指数(FIC)高达 1.0,这表明与 hLF(1-11) 联合使用时,抗真菌药物的药效具有协同或叠加效应:结果表明,hLF(1-11)可与氟康唑或两性霉素联合用于耐药菌株的抗菌治疗,增强这些抗真菌药物的效力,从而改善患者的治疗效果。
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Combinatory Use of hLF(1-11), a Synthetic Peptide Derived from Human Lactoferrin, and Fluconazole/Amphotericin B against Malassezia furfur Reveals a Synergistic/Additive Antifungal Effect.

Objective: The increasing resistance of Malassezia yeasts against commonly used antifungal drugs dictates the need for novel antifungal compounds. Human lactoferrin-based peptides show a broad spectrum of antimicrobial activities. Various assays were performed to find the optimal growth conditions of the yeasts and to assess cell viability, using media with low lipid content to avoid peptide binding to medium components.

Methods: In the current study, we tested the antimicrobial susceptibility of 30 strains of M. furfur that cover the known IGS1 genotypic variation.

Results: hLF(1-11) inhibited the growth of all species tested, resulting in minimum inhibitory concentrations (MIC) values ranging from 12.5 to 100 μg/mL. In the combinatory tests, the majority of fractional inhibitory concentration indexes (FIC) for the tested strains of M. furfur were up to 1.0, showing that there is a synergistic or additive effect on the efficacy of the antifungal drugs when used in combination with hLF(1-11).

Conclusion: Results showed that hLF(1-11) could be combined with fluconazole or amphotericin for the antimicrobial treatment of resistant strains, enhancing the potency of these antifungal drugs, resulting in an improved outcome for the patient.

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来源期刊
Antibiotics-Basel
Antibiotics-Basel Pharmacology, Toxicology and Pharmaceutics-General Pharmacology, Toxicology and Pharmaceutics
CiteScore
7.30
自引率
14.60%
发文量
1547
审稿时长
11 weeks
期刊介绍: Antibiotics (ISSN 2079-6382) is an open access, peer reviewed journal on all aspects of antibiotics. Antibiotics is a multi-disciplinary journal encompassing the general fields of biochemistry, chemistry, genetics, microbiology and pharmacology. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of papers.
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