Institute of Microbiology, University Hospital Center and University of Lausanne, Lausanne, Switzerland.
Virology. 2012 Feb 5;423(1):14-22. doi: 10.1016/j.virol.2011.11.008. Epub 2011 Dec 10.
The cellular protease subtilisin kexin isozyme-1 (SKI-1)/site-1 protease (S1P) is implicated in the proteolytic processing of the viral envelope glycoprotein precursor (GPC) of arenaviruses, a step strictly required for production of infectious progeny. The small molecule SKI-1/S1P inhibitor PF-429242 was shown to have anti-viral activity against Old World arenaviruses. Here we extended these studies and show that PF-429242 also inhibits GPC processing and productive infection of New World arenaviruses, making PF-429242 a broadly active anti-arenaviral drug. In combination therapy, PF-429242 potentiated the anti-viral activity of ribavirin, indicating a synergism between the two drugs. A hallmark of arenaviruses is their ability to establish persistent infection in vitro and in vivo. Notably, PF-429242 was able to efficiently and rapidly clear persistent infection by arenaviruses. Interruption of drug treatment did not result in re-emergence of infection, indicating that PF-429242 treatment leads to virus extinction.
细胞蛋白酶枯草杆菌蛋白酶/kexin 同种型-1(SKI-1)/位点-1 蛋白酶(S1P)参与沙粒病毒包膜糖蛋白前体(GPC)的蛋白水解加工,这是产生感染性后代的严格要求步骤。小分子 SKI-1/S1P 抑制剂 PF-429242 已被证明对旧世界沙粒病毒具有抗病毒活性。在这里,我们扩展了这些研究,并表明 PF-429242 还抑制新世界沙粒病毒的 GPC 加工和有效感染,使 PF-429242 成为一种广泛有效的抗沙粒病毒药物。在联合治疗中,PF-429242 增强了利巴韦林的抗病毒活性,表明这两种药物具有协同作用。沙粒病毒的一个标志是它们在体外和体内建立持续性感染的能力。值得注意的是,PF-429242 能够有效地迅速清除沙粒病毒的持续性感染。中断药物治疗不会导致感染再次出现,表明 PF-429242 治疗导致病毒灭绝。