Departamento de Microbiologia Geral, Instituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Programa de Biologia Celular e Parasitologia, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Front Cell Infect Microbiol. 2021 Jul 23;11:698662. doi: 10.3389/fcimb.2021.698662. eCollection 2021.
and species are filamentous fungi responsible for a wide range of infections in humans and are frequently associated with cystic fibrosis and immunocompromising conditions. Because they are usually resistant to many antifungal drugs available in clinical settings, studies of alternative targets in fungal cells and therapeutic approaches are necessary. In the present work, we evaluated the antifungal activity of miltefosine against and species and how this phospholipid analogue affects the fungal cell. Miltefosine inhibited different and species at 2-4 µg/ml and reduced biofilm formation. The loss of membrane integrity in caused by miltefosine was demonstrated by leakage of intracellular components and lipid raft disorganisation. The exogenous addition of glucosylceramide decreased the inhibitory activity of miltefosine. Reactive oxygen species production and mitochondrial activity were also affected by miltefosine, as well as the susceptibility to fluconazole, caspofungin and myoricin. The data obtained in the present study contribute to clarify the dynamics of the interaction between miltefosine and and cells, highlighting its potential use as new antifungal drug in the future.
和 物种是丝状真菌,可导致人类发生广泛的感染,且常与囊性纤维化和免疫功能低下有关。由于这些真菌通常对临床环境中可用的许多抗真菌药物具有耐药性,因此有必要研究真菌细胞中的替代靶标和治疗方法。在本工作中,我们评估了米替福新对 和 物种的抗真菌活性,以及这种磷脂类似物如何影响真菌细胞。米替福新以 2-4μg/ml 的浓度抑制不同的 和 物种,并减少生物膜形成。米替福新导致 的细胞膜完整性丧失,这通过细胞内成分的渗漏和脂筏结构紊乱得到证明。葡糖脑苷脂的外源添加降低了米替福新的抑制活性。米替福新还影响活性氧物质的产生和线粒体活性,以及对氟康唑、卡泊芬净和米卡芬净的敏感性。本研究获得的数据有助于阐明米替福新与 和 细胞相互作用的动态,突出了其在未来作为新型抗真菌药物的潜在用途。