School of Biosciences, Institute of Microbiology and Infection, University of Birmingham, Birmingham, United Kingdom.
Department of Biochemistry and Molecular Biology, Monash University, Clayton, VIC, Australia.
Front Cell Infect Microbiol. 2019 May 29;9:181. doi: 10.3389/fcimb.2019.00181. eCollection 2019.
The incidence of fungal diseases is on the rise and the number of fatalities is still unacceptably high. While advances into antifungal drug development have been made there remains an urgent need to develop novel antifungal agents targeting as-yet unexploited pathways, such as metal ion homeostasis. Here we report such an approach by developing a metal sensor screen in the opportunistic human fungal pathogen . Using this reporter strain, we screened a library of 1,200 compounds and discovered several active compounds not previously described as chemical entities with antifungal properties. Two of these, artemisinin and pyrvinium pamoate, have been further characterized and their interference with metal homeostasis and potential as novel antifungal compounds validated. Lastly, we demonstrate that the same strain can be used to report on intracellular conditions within host phagocytes, paving the way toward the development of novel screening platforms that could identify compounds with the potential to perturb ion homeostasis of the pathogen specifically within host cells.
真菌感染的发病率正在上升,死亡率仍然高得令人无法接受。虽然在抗真菌药物开发方面已经取得了进展,但仍迫切需要开发针对尚未开发的途径的新型抗真菌药物,例如金属离子稳态。在这里,我们通过开发机会性人类真菌病原体中的金属传感器筛选报告了这样一种方法。 使用该报告菌株,我们筛选了 1200 种化合物的文库,并发现了几种以前未被描述为具有抗真菌特性的化学实体的活性化合物。其中两种,青蒿素和吡喹酮,已进一步进行了表征,并验证了它们对金属稳态的干扰及其作为新型抗真菌化合物的潜力。最后,我们证明相同的菌株可用于报告宿主吞噬细胞内的细胞内情况,为开发新型筛选平台铺平了道路,这些平台可以鉴定具有潜在破坏病原体离子稳态的化合物,特别是在宿主细胞内。