National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Inada-cho, Obihiro, Hokkaido 080-8555, Japan; Department of Pre-clinical and Applied Animal Science, Faculty of Veterinary Science, Mahidol University, 999 Phutthamonthon Sai 4 Road Salaya, Phutthamonthon Nakhonpathom 73170, Thailand.
Institute of Microbial Chemistry (BIKAKEN), Shizuoka 410-0301, Japan.
Parasitol Int. 2021 Apr;81:102267. doi: 10.1016/j.parint.2020.102267. Epub 2020 Dec 8.
Metacytofilin (MCF) was isolated from the fungus Metarhizium sp. TA2759. Although MCF possesses anti-Toxoplasma activity, the effects of this compound against other parasites are unknown. Here, we evaluated the in vitro anti-malarial activity of MCF against the 3D7 strain and the chloroquine-resistant K1 strain of Plasmodium falciparum. The half maximal inhibitory concentrations (IC) of MCF against the 3D7 and K-1 strains following culture for 48 h were 666 nM and 605 nM, respectively. Artemisinin was more potent than MCF against both strains (3D7 IC: 17.4 nM; K-1 IC: 18.3 nM), while chloroquine was ineffective against the chloroquine-resistant strain (3D7 IC: 39.1 nM; K-1 IC: 1.62 μM). MCF affected the ring stage of the parasites, resulting in their death as shown by spots within red blood cells. MCF also inhibited parasite growth following culture for 72 h (3D7 IC, 285 nM). Four optical isomers of cyclo[Leu-Phe]-diketopiperazine derivatives with modified methoxy and/or hydroxyl groups lost anti-malarial activity, suggesting that the spatial positions of the methoxy and hydroxyl groups in MCF play an important role in its anti-malarial effects. Together, these data suggest that MCF may represent a promising lead compound for treatment of drug-resistant malarial parasites.
微管相关蛋白(MCF)是从真菌玫烟色棒束孢 TA2759 中分离得到的。虽然 MCF 具有抗弓形虫活性,但该化合物对其他寄生虫的作用尚不清楚。在此,我们评估了 MCF 对 3D7 株和耐氯喹的恶性疟原虫 K1 株的体外抗疟活性。MCF 对 3D7 和 K-1 株培养 48 小时后的半抑制浓度(IC)分别为 666 nM 和 605 nM。青蒿素对两种株系的活性均强于 MCF(3D7 IC:17.4 nM;K-1 IC:18.3 nM),而氯喹对耐氯喹株系无效(3D7 IC:39.1 nM;K-1 IC:1.62 μM)。MCF 影响寄生虫的环早期阶段,导致其死亡,红细胞内出现斑点。MCF 还抑制培养 72 小时后的寄生虫生长(3D7 IC:285 nM)。四种光学异构体的环[Leu-Phe]-二酮哌嗪衍生物,其甲氧基和/或羟基被修饰,失去了抗疟活性,这表明 MCF 中甲氧基和羟基的空间位置对其抗疟作用很重要。综上所述,这些数据表明 MCF 可能代表一种有前途的抗耐药疟原虫药物的先导化合物。