Department of Chemical and Biomolecular Engineering, University of Maryland.
Department of Chemical and Biomolecular Engineering, University of Maryland;
J Vis Exp. 2023 Jan 13(191). doi: 10.3791/64416.
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.
传统的白色念珠菌抗真菌药敏试验方法耗时且缺乏定量结果。例如,一种常见的方法是将用不同浓度抗真菌分子处理的细胞接种在琼脂平板上,然后计算菌落数,以确定分子浓度与生长抑制之间的关系。这种方法需要许多平板和大量时间来计数菌落。另一种常见的方法通过观察用抗真菌剂处理的培养物来消除平板和菌落的计数,以确定抑制生长所需的最小浓度;然而,肉眼观察只能产生定性结果,并且失去了亚抑制浓度下生长的信息。本方案描述了一种测量白色念珠菌对抗真菌肽敏感性的方法。通过依赖于培养物的光密度测量,该方法减少了获得不同肽浓度下培养物生长的定量结果所需的时间和材料。用适当的缓冲液在 96 孔板中孵育真菌与肽,对照代表无生长抑制和完全生长抑制。用肽孵育后,将所得细胞悬浮液稀释以降低肽活性,然后过夜生长。过夜生长后,测量每个孔的光密度,并与阳性和阴性对照进行比较,以计算每个肽浓度下的生长抑制率。该测定法的结果与在琼脂平板上培养物的传统平板法相当,但该方案减少了塑料废物和计数菌落的时间。虽然该方案的应用主要集中在抗真菌肽上,但该方法也将适用于测试具有已知或疑似抗真菌活性的其他分子。