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全球卫生重点 Box Ⓡ 筛查显示,针对新兴的多药耐药病原体耳念珠菌,可能有新的消毒剂。

Screening of the global health priority BoxⓇ reveals potential new disinfectants against the emerging multidrug-resistant pathogen Candida auris.

机构信息

Health Sciences Research Laboratory, Federal University of Grande Dourados, Dourados, Mato Grosso do Sul, Brazil.

Instituto Carlos Chagas, Fundação Oswaldo Cruz (Fiocruz), Curitiba, Brazil.

出版信息

Microb Pathog. 2024 Sep;194:106828. doi: 10.1016/j.micpath.2024.106828. Epub 2024 Jul 28.

Abstract

BACKGROUND

Candida auris has been identified by the World Health Organization as a critical pathogen due to its invasive nature, resistance to multiple drugs, and high mortality rates in hospital outbreaks. This fungus can persist on surfaces and human skin for extended periods, complicating infection control efforts. The need for effective disinfection strategies is urgent, as current disinfectants are often ineffective against C. auris biofilms.

OBJECTIVE

The study aimed to identify potential disinfectants from a collection of 240 compounds in the Global Health Priority Box® that are effective against C. auris, particularly strains resistant to existing options.

METHODS

The research employed a screening protocol using a fluconazole-resistant strain of C. auris (149/23). Antifungal activity was assessed using the microdilution method to determine Minimum Inhibitory Concentrations (MICs) and Minimum Fungicidal Concentrations (MFCs). Additional assays were conducted to evaluate biofilm inhibition, biofilm eradication, cell membrane integrity, nucleotide leakage, sorbitol protection assay, efflux pump inhibition, and hemolysis assay.

RESULTS

Two compounds, Hydramethylnon (MMV1577471) and Flufenerim (MMV1794206), demonstrated significant inhibitory effects against C. auris. Hydramethylnon exhibited potent antifungal activity, inhibiting up to 93 % of fungal growth with an MFC of 16 μg/mL. Flufenerim inhibited up to 58 % of fungal growth, showing fungistatic action with an MFC greater than 4 μg/mL. Biofilm inhibition tests showed that both compounds significantly inhibited biofilm formation, with increased efficacy at higher concentrations. Both compounds showed eradication rates in both stages. Furthermore, Hydramethylnon and Flufenerim did not affect cell membrane integrity or nucleotide leakage, suggesting a mode of action not reliant on disrupting these cellular components. The sorbitol protection assay revealed that neither compound caused cell wall damage. In the efflux pump inhibition assay, Hydramethylnon did not activate efflux pumps, while Flufenerim activated efflux pumps, reducing its effectiveness. Hemocompatibility assay showed safety.

CONCLUSION

The study highlights Hydramethylnon and Flufenerim as promising candidates for further development as disinfectants, offering potential solutions to the urgent need for effective disinfection agents against C. auris. The findings underscore the value of screening compound collections to identify novel antifungal agents and understand their mechanisms of action, thereby contributing to the advancement of new disinfection strategies in healthcare settings.

摘要

背景

由于侵袭性、对多种药物的耐药性以及医院爆发时的高死亡率,耳念珠菌已被世界卫生组织确认为一种关键病原体。这种真菌可以在表面和人体皮肤上长时间存活,这使得感染控制工作变得复杂。由于目前的消毒剂通常对耳念珠菌生物膜无效,因此迫切需要有效的消毒策略。

目的

本研究旨在从全球卫生重点药物清单中 240 种化合物中筛选出对耳念珠菌有效的潜在消毒剂,特别是对现有选择具有耐药性的菌株。

方法

本研究采用了一种筛选方案,使用氟康唑耐药的耳念珠菌(149/23)菌株。使用微量稀释法测定最小抑菌浓度(MIC)和最小杀菌浓度(MFC)来评估抗真菌活性。还进行了其他测定,以评估生物膜抑制、生物膜清除、细胞膜完整性、核苷酸渗漏、山梨醇保护试验、外排泵抑制和溶血试验。

结果

两种化合物,Hydramethylnon(MMV1577471)和 Flufenerim(MMV1794206),对耳念珠菌表现出显著的抑制作用。Hydramethylnon 表现出很强的抗真菌活性,其 MFC 为 16μg/ml 时,可抑制高达 93%的真菌生长。Flufenerim 抑制了高达 58%的真菌生长,其 MFC 大于 4μg/ml 时表现出抑菌作用。生物膜抑制试验表明,两种化合物均能显著抑制生物膜形成,且在较高浓度时效果更佳。两种化合物均在两个阶段均有清除作用。此外,Hydramethylnon 和 Flufenerim 均不影响细胞膜完整性或核苷酸渗漏,这表明其作用模式不依赖于破坏这些细胞成分。山梨醇保护试验表明,这两种化合物均不会导致细胞壁损伤。在外排泵抑制试验中,Hydramethylnon 不会激活外排泵,而 Flufenerim 会激活外排泵,从而降低其效果。溶血试验表明其具有安全性。

结论

本研究强调了 Hydramethylnon 和 Flufenerim 作为消毒剂进一步开发的有希望的候选物,为对抗耳念珠菌急需有效的消毒剂提供了潜在的解决方案。这些发现突出了筛选化合物库以鉴定新型抗真菌剂并了解其作用机制的价值,从而为在医疗保健环境中推进新的消毒策略做出贡献。

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