Štefánik Michal, Bhosale Dattatry Shivajirao, Haviernik Jan, Straková Petra, Fojtíková Martina, Dufková Lucie, Huvarová Ivana, Salát Jiří, Bartáček Jan, Svoboda Jan, Sedlák Miloš, Růžek Daniel, Miller Andrew D, Eyer Luděk
Laboratory of Emerging Viral Diseases, Veterinary Research Institute, Hudcova 296/70, CZ-621 00 Brno, Czech Republic.
Department of Chemistry and Biochemistry, Mendel University in Brno, Zemědělská 1665/1, CZ-613 00 Brno, Czech Republic.
Viruses. 2022 Feb 9;14(2):354. doi: 10.3390/v14020354.
Diphyllin is a natural arylnaphtalide lignan extracted from tropical plants of particular importance in traditional Chinese medicine. This compound has been described as a potent inhibitor of vacuolar (H)ATPases and hence of the endosomal acidification process that is required by numerous enveloped viruses to trigger their respective viral infection cascades after entering host cells by receptor-mediated endocytosis. Accordingly, we report here a revised, updated, and improved synthesis of diphyllin, and demonstrate its antiviral activities against a panel of enveloped viruses from and families. Diphyllin is not cytotoxic for Vero and BHK-21 cells up to 100 µM and exerts a sub-micromolar or low-micromolar antiviral activity against tick-borne encephalitis virus, West Nile virus, Zika virus, Rift Valley fever virus, rabies virus, and herpes-simplex virus type 1. Our study shows that diphyllin is a broad-spectrum host cell-targeting antiviral agent that blocks the replication of multiple phylogenetically unrelated enveloped RNA and DNA viruses. In support of this, we also demonstrate that diphyllin is more than just a vacuolar (H)ATPase inhibitor but may employ other antiviral mechanisms of action to inhibit the replication cycles of those viruses that do not enter host cells by endocytosis followed by low pH-dependent membrane fusion.
双氢槲皮素是一种从热带植物中提取的天然芳基萘内酯木脂素,在传统中药中具有特殊重要性。该化合物已被描述为液泡(H)ATP酶的有效抑制剂,因此也是内体酸化过程的抑制剂,许多包膜病毒通过受体介导的内吞作用进入宿主细胞后,需要内体酸化过程来触发各自的病毒感染级联反应。因此,我们在此报告双氢槲皮素的一种修订、更新和改进的合成方法,并证明其对一组来自不同科的包膜病毒具有抗病毒活性。双氢槲皮素在浓度高达100μM时对Vero细胞和BHK - 21细胞无细胞毒性,对蜱传脑炎病毒、西尼罗河病毒、寨卡病毒、裂谷热病毒、狂犬病病毒和1型单纯疱疹病毒具有亚微摩尔或低微摩尔的抗病毒活性。我们的研究表明,双氢槲皮素是一种广谱的靶向宿主细胞的抗病毒剂,可阻断多种系统发育无关的包膜RNA和DNA病毒的复制。为此,我们还证明双氢槲皮素不仅仅是一种液泡(H)ATP酶抑制剂,还可能采用其他抗病毒作用机制来抑制那些不通过内吞作用进入宿主细胞随后进行低pH依赖性膜融合的病毒的复制周期。