Wu Lei, Yuan Ye, Zhao Zhenchao, Yan Ya, Wang Haiwei, Li Xin
National Key Laboratory of Veterinary Public Health and Safety, College of Veterinary Medicine, China Agricultural University, Beijing 100193, China; Key Laboratory of Animal Epidemiology of the Ministry of Agriculture and Rural Affairs, College of Veterinary Medicine, China Agricultural University, Beijing 100193, China.
State Key Laboratory of Animal Disease Control, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin 150069, China.
Int J Biol Macromol. 2025 May;306(Pt 3):141587. doi: 10.1016/j.ijbiomac.2025.141587. Epub 2025 Mar 1.
Seneca Valley Virus (SVV) is a picornavirus that causes vesicular lesions in pigs, significantly affecting global swine farming. The SVV 3C protease is essential for processing the viral polyprotein and facilitates immune evasion by cleaving or degrading multiple innate immune proteins. In this study, we identified three caspase inhibitors, including Z-VAD(OMe)-FMK (Z-VAD), Z-FA-FMK (Z-FA), and Z-VDVAD-FMK (Z-VDVAD), which significantly inhibit the cleavage activity of SVV 3C protease using a recombinant protein system. Comparative analysis revealed that Z-VAD exhibited the most potent inhibitory effect in a cell transfection system. Further investigations confirmed that Z-VAD, Z-FA, and Z-VDVAD bound directly to the 3C protein. Molecular docking analysis showed that Z-VAD interacted with key enzymatic site residues His48 and Cys160 of the 3C protease, while Z-VDVAD and Z-FA interacted only with residue Cys160. Infection experiments demonstrated that Z-VAD significantly suppressed the replication by targeting 3C protease. Furthermore, Z-VAD significantly suppressed the replication of Enterovirus A71 (EV-A71) and encephalomyocarditis virus (EMCV). Our findings provide a comprehensive understanding of SVV 3C protease inhibitors and their mechanisms of action, offering valuable insights for the development of strategies to control SVV and other picornaviruses.
塞内卡山谷病毒(SVV)是一种小核糖核酸病毒,可在猪身上引起水疱性病变,对全球养猪业产生重大影响。SVV 3C蛋白酶对于加工病毒多聚蛋白至关重要,并通过切割或降解多种先天免疫蛋白促进免疫逃逸。在本研究中,我们鉴定出三种半胱天冬酶抑制剂,包括Z-VAD(OMe)-FMK(Z-VAD)、Z-FA-FMK(Z-FA)和Z-VDVAD-FMK(Z-VDVAD),它们使用重组蛋白系统可显著抑制SVV 3C蛋白酶的切割活性。比较分析表明,Z-VAD在细胞转染系统中表现出最有效的抑制作用。进一步研究证实,Z-VAD、Z-FA和Z-VDVAD直接与3C蛋白结合。分子对接分析表明,Z-VAD与3C蛋白酶的关键酶位点残基His48和Cys160相互作用,而Z-VDVAD和Z-FA仅与残基Cys160相互作用。感染实验表明,Z-VAD通过靶向3C蛋白酶显著抑制病毒复制。此外,Z-VAD显著抑制肠道病毒A71(EV-A71)和脑心肌炎病毒(EMCV)的复制。我们的研究结果全面了解了SVV 3C蛋白酶抑制剂及其作用机制,为制定控制SVV和其他小核糖核酸病毒的策略提供了有价值的见解。