Quantifying the Antifungal Activity of Peptides Against <em>Candida albicans</em>

白色念珠菌 生长抑制 琼脂 孵化 琼脂平板 抗真菌 白色体 细胞计数 电镀效率 生物 光密度 微生物学 真菌 生长培养基 化学 生物化学 细胞生长 体外 细胞 细菌 医学 植物 遗传学 细胞周期 眼科
作者
Wright K. Makambi,Svetlana P. Ikonomova,Amy J. Karlsson
出处
期刊:Journal of Visualized Experiments [MyJoVE Corporation]
卷期号: (191) 被引量:1
标识
DOI:10.3791/64416
摘要

Traditional methods for performing antifungal susceptibility testing for Candida albicans are time-consuming and lack quantitative results. For example, a common approach relies on plating cells treated with different concentrations of antifungal molecules on agar plates and then counting the colonies to determine the relationship between molecule concentration and growth inhibition. This method requires many plates and substantial time to count the colonies. Another common approach eliminates the plates and counting of colonies by visually inspecting cultures treated with antifungal agents to identify the minimum concentration required to inhibit growth; however, visual inspection produces only qualitative results, and information on growth at subinhibitory concentrations is lost. This protocol describes a method for measuring the susceptibility of C. albicans to antifungal peptides. By relying on optical density measurements of cultures, the method reduces the time and materials needed to obtain quantitative results on culture growth at different peptide concentrations. The incubation of the fungus with peptides is performed in a 96-well plate using an appropriate buffer, with controls representing no growth inhibition and complete growth inhibition. Following the incubation with the peptide, the resulting cell suspensions are diluted to reduce peptide activity and then grown overnight. After overnight growth, the optical density of each well is measured and compared to the positive and negative controls to calculate the resulting growth inhibition at each peptide concentration. The results using this assay are comparable to the results using the traditional method of plating the cultures on agar plates, but this protocol reduces plastic waste and the time spent on counting colonies. Although the applications of this protocol have focused on antifungal peptides, the method will also be applicable to testing other molecules with known or suspected antifungal activity.

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