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Antiviral effects of a thiol protease inhibitor on foot-and-mouth disease virus.

机译:硫醇蛋白酶抑制剂对口蹄疫病毒的抗病毒作用。

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摘要

The thiol protease inhibitor E-64 specifically blocks autocatalytic activity of the leader protease of foot-and-mouth disease virus (FMDV) and interferes with cleavage of the structural protein precursor in an in vitro translation assay programmed with virion RNA. Experiments with FMDV-infected cells and E-64 or a membrane-permeable analog, E-64d, have confirmed these results and demonstrated interference in virus assembly, causing a reduction in virus yield. In addition, there is a lag in the appearance of virus-induced cellular morphologic alterations, a delay in cleavage of host cell protein p220 and in shutoff of host protein synthesis, and a decrease in viral protein and RNA synthesis. The implications of using E-64-based compounds as potential antiviral agents for FMDV are discussed.
机译:硫醇蛋白酶抑制剂E-64特异性阻断口蹄疫病毒(FMDV)的前导蛋白酶的自催化活性,并在通过病毒体RNA编程的体外翻译测定中干扰结构蛋白前体的裂解。用FMDV感染的细胞和E-64或可透过膜的类似物E-64d进行的实验已证实了这些结果,并证明了对病毒装配的干扰,导致病毒产量降低。另外,在病毒诱导的细胞形态学改变的出现,宿主细胞蛋白p220的切割的延迟和宿主蛋白合成的延迟以及病毒蛋白和RNA合成的减少方面存在滞后。讨论了使用基于E-64的化合物作为FMDV的潜在抗病毒药的意义。

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