The Graduate School, University of Santo Tomas, España Blvd., Manila 1015, Philippines.
UST Laboratories for Vaccine Science, Molecular Biology and Biotechnology, Research Center for the Natural and Applied Sciences, University of Santo Tomas, España Blvd., Manila 1015, Philippines.
Biomolecules. 2024 May 22;14(6):610. doi: 10.3390/biom14060610.
Candidiasis is considered an emerging public health concern because of the occurrence of drug-resistant strains and the lack of an available structurally diverse antifungal drug armamentarium. The indole alkaloid globospiramine from the anticandidal Philippine medicinal plant exhibits a variety of biological activities; however, its antifungal properties remain to be explored. In this study, we report the in vitro anticandidal activities of globospiramine against two clinically relevant species ( and ) and the exploration of its possible target proteins using in silico methods. Thus, the colony-forming unit (CFU) viability assay revealed time- and concentration-dependent anticandidal effects of the alkaloid along with a decrease in the number of viable CFUs by almost 50% at 60 min after treatment. The results of the MIC and MFC assays indicated inhibitory and fungicidal effects of globospiramine against (MIC = 8 µg/mL; MFC = 8 µg/mL) and potential fungistatic effects against at lower concentrations (MIC = 4 µg/mL; MFC > 64 µg/mL). The FAM-FLICA poly-caspase assay showed metacaspase activation in cells at concentrations of 16 and 8 µg/mL, which agreed well with the MIC and MFC values. Molecular docking and molecular dynamics simulation experiments suggested globospiramine to bind strongly with 1,3-β-glucan synthase and Als3 adhesin-enzymes indirectly involved in apoptosis-driven candidal inhibition.
念珠菌病被认为是一个新出现的公共卫生问题,原因是耐药菌株的出现和缺乏结构多样的可用抗真菌药物武器库。具有抗真菌活性的菲律宾药用植物中分离得到的吲哚生物碱 globospiramine 具有多种生物活性,但它的抗真菌特性仍有待探索。在这项研究中,我们报告了 globospiramine 对两种临床相关物种( 和 )的体外抗真菌活性,并通过计算方法探索了其可能的靶蛋白。因此,集落形成单位(CFU)活力测定显示该生物碱具有时间和浓度依赖性的抗真菌作用,并且在处理后 60 分钟内,活 CFU 的数量减少了近 50%。MIC 和 MFC 测定结果表明 globospiramine 对 (MIC = 8 µg/mL;MFC = 8 µg/mL)具有抑制和杀菌作用,对 较低浓度(MIC = 4 µg/mL;MFC > 64 µg/mL)具有潜在的抑菌作用。FAM-FLICA 多半胱氨酸酶检测试剂盒显示 16 和 8 µg/mL 浓度下 细胞中的半胱天冬酶被激活,这与 MIC 和 MFC 值吻合较好。分子对接和分子动力学模拟实验表明,globospiramine 与 1,3-β-葡聚糖合酶和 Als3 黏附酶强烈结合,后者间接参与了凋亡驱动的念珠菌抑制。