生物源银纳米颗粒通过细胞内ROS的产生对白色念珠菌具有抗真菌和抗生物膜活性

IF 2.6 4区 医学 Q4 IMMUNOLOGY
Apmis Pub Date : 2025-08-17 DOI:10.1111/apm.70061
Nidhi Chandrakar, Sudhir K. Shukla, Dugeshwar Karley, Namrata Upadhyay, Y. V. Nancharaiah
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引用次数: 0

摘要

白色念珠菌抗真菌耐药性的出现要求开发新的治疗策略。本研究评价了腐生葡萄球菌细菌上清液合成的生物源银纳米颗粒(bAgNPs)的抗真菌和抗生物膜活性。紫外可见光谱证实了bAgNPs的形成,在418 nm处有明显的吸光度峰。最低抑菌浓度(MIC)测定表明,50 μg/mL能有效抑制真菌生长。结晶紫染色和荧光显微镜显示,bAgNPs显著降低了生物膜生物量,80 μg/mL浓度的bAgNPs减少了70%以上。机制研究表明,bAgNPs诱导活性氧(ROS)产生,荧光强度在80 μg/mL时达到峰值,导致氧化应激介导的细胞死亡。酵母到菌丝的转化是一个关键的毒力机制,被抑制,阻碍了真菌的入侵。此外,SYTO 9/碘化丙啶染色证实了细胞膜完整性的破坏,其中超过60%的细胞在MIC上显示出受损的膜。MTT分析结果表明,在MIC下,bAgNPs通过降低75%的代谢活性来损害线粒体功能。这些发现表明bAgNPs靶向多种关键途径,包括ros介导的氧化损伤、膜破坏和代谢损伤,从而发挥强大的抗真菌作用;因此,他们提出了一种治疗生物膜相关白色念珠菌感染的有希望的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Biogenic Silver Nanoparticles Exhibit Antifungal and Antibiofilm Activity Against Candida albicans via Intracellular ROS Production

Biogenic Silver Nanoparticles Exhibit Antifungal and Antibiofilm Activity Against Candida albicans via Intracellular ROS Production

The emergence of antifungal resistance in Candida albicans necessitates the development of novel therapeutic strategies. This study evaluates the antifungal and antibiofilm activity of biogenic silver nanoparticles (bAgNPs) synthesized using Staphylococcus saprophyticus bacterial supernatant. UV–Visible spectroscopy confirmed the formation of bAgNPs, with a distinct absorbance peak at 418 nm. Minimum inhibitory concentration (MIC) testing determined that 50 μg/mL effectively inhibited fungal growth. bAgNPs significantly reduced biofilm biomass, with an 80 μg/mL concentration resulting in over a 70% reduction, as demonstrated by crystal violet staining and fluorescence microscopy. Mechanistic studies revealed that bAgNPs induced reactive oxygen species (ROS) production, with fluorescence intensity peaking at 80 μg/mL, leading to oxidative stress-mediated cell death. The yeast-to-hyphal transition, a key virulence mechanism, was inhibited, impeding the fungal invasiveness. Furthermore, the disruption of cell membrane integrity was confirmed by SYTO 9/propidium iodide staining, where over 60% of cells displayed compromised membranes at MIC. MTT assay results demonstrated that bAgNPs impaired mitochondrial function by reducing metabolic activity by 75% at MIC. These findings suggest that bAgNPs target multiple critical pathways, including ROS-mediated oxidative damage, membrane disruption, and metabolic impairment, thereby exerting a potent antifungal effect; thus, they present a promising approach for treating biofilm-associated C. albicans infections.

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来源期刊
Apmis
Apmis 医学-病理学
CiteScore
5.20
自引率
0.00%
发文量
91
审稿时长
2 months
期刊介绍: APMIS, formerly Acta Pathologica, Microbiologica et Immunologica Scandinavica, has been published since 1924 by the Scandinavian Societies for Medical Microbiology and Pathology as a non-profit-making scientific journal.
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