PF-00835231 broadly inhibits swine Alpha-coronavirus, including emerging SADS-CoV.

IF 4 2区 医学 Q2 VIROLOGY Journal of Virology Pub Date : 2024-11-19 Epub Date: 2024-10-31 DOI:10.1128/jvi.01303-24
Lei Shi, Yueyue Duan, Liyan Cao, Yu Zhang, Cong Yuan, Maowen Sun, Juan Zhang, Xiangyu Kong, Haixue Zheng, Qi Wang
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Abstract

Swine Alpha-coronaviruses are one of the most destructive pathogens affecting the swine industries across the world. Swine Alpha-coronaviruses include transmissible gastroenteritis virus (TGEV), porcine epidemic diarrhea virus, porcine respiratory coronavirus, and swine acute diarrhea syndrome coronavirus (SADS-CoV). Thus far, swine Alpha-coronaviruses treatment options are very limited. Therefore, the identification of safe and effective treatment of swine Alpha-coronaviruses is urgently needed. In the current study, we screened a library of 240 FDA-approved compounds for antiviral activity against TGEV. Among screening, the 3CL protease inhibitor PF-00835231 was shown to dramatically inhibit TGEV replication in vitro systems. Mechanistically, PF-00835231 inhibits nonstructural protein 5 (Nsp5) protease activity targeting the cleavage at Nsp5-Nsp6 of TGEV. Additionally, PF-00835231 exhibited the potent broad-spectrum swine Alpha-coronaviruses antiviral activity. Treatment of PF-00835231 in mice not only blocks SADS-CoV deadly infection but also dramatically reduces viral copies. Taken together, our study provides evidence that PF-00835231 may control of the current swine Alpha-coronaviruses and emerging swine Alpha-coronaviruses in the future.IMPORTANCEThe COVID-19 pandemic has induced tremendous efforts to develop therapeutic strategies that target Beta-coronavirus including SARS-CoV-2. 3CL protease of Beta-coronavirus has been as a drug target for developing antiviral drugs. However, 3CL protease is not conserved in Alpha-coronavirus and Beta-coronavirus with only 44% amino acid similarity. Therefore, an inhibitor that prevents Alpha-coronaviruses infection is urgently needed. Swine Alpha-coronaviruses are one of the most destructive pathogens affecting the swine industries across the world. Swine herds with coronavirus diarrhea showed a high rate of co-infection between different Alpha-coronavirus. Our study, for the first time, showed that PF-00835231 inhibits swine Alpha-coronavirus infection. At the mechanistic level, we experimentally identified that PF-00835231 inhibits nonstructural protein 5 (Nsp5) protease activity targeting the cleavage at Nsp5-Nsp6 of Alpha-coronaviruses.

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PF-00835231 可广泛抑制猪α-冠状病毒,包括新出现的 SADS-CoV。
猪α-冠状病毒是影响全球养猪业最具破坏性的病原体之一。猪α-冠状病毒包括传染性胃肠炎病毒(TGEV)、猪流行性腹泻病毒、猪呼吸道冠状病毒和猪急性腹泻综合征冠状病毒(SADS-CoV)。迄今为止,猪α-冠状病毒的治疗方案非常有限。因此,迫切需要找到安全有效的治疗猪阿尔法冠状病毒的方法。在本研究中,我们筛选了 240 种美国 FDA 批准的化合物库,以检测其对 TGEV 的抗病毒活性。筛选结果表明,3CL蛋白酶抑制剂PF-00835231能显著抑制TGEV在体外系统中的复制。从机理上讲,PF-00835231 可抑制非结构蛋白 5(Nsp5)蛋白酶的活性,从而抑制 TGEV Nsp5-Nsp6 的裂解。此外,PF-00835231 还具有强效的广谱猪α-冠状病毒抗病毒活性。用 PF-00835231 治疗小鼠不仅能阻断 SADS-CoV 的致命感染,还能显著减少病毒拷贝数。总之,我们的研究为 PF-00835231 提供了证据,证明它可以控制目前的猪α-冠状病毒和未来新出现的猪α-冠状病毒。 重要意义COVID-19 大流行促使人们大力开发针对 Beta 冠状病毒(包括 SARS-CoV-2)的治疗策略。Beta 冠状病毒的 3CL 蛋白酶一直是开发抗病毒药物的药物靶点。然而,3CL 蛋白酶在阿尔法-冠状病毒和贝塔-冠状病毒中并不保守,只有 44% 的氨基酸相似。因此,迫切需要一种能预防阿尔法-冠状病毒感染的抑制剂。猪α-冠状病毒是影响全球养猪业的最具破坏性的病原体之一。冠状病毒腹泻的猪群显示出不同阿尔法-冠状病毒之间的高合并感染率。我们的研究首次表明,PF-00835231 可抑制猪阿尔法冠状病毒感染。在机理层面,我们通过实验发现,PF-00835231 可抑制非结构蛋白 5(Nsp5)蛋白酶的活性,从而抑制阿尔法冠状病毒 Nsp5-Nsp6 的裂解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Virology
Journal of Virology 医学-病毒学
CiteScore
10.10
自引率
7.40%
发文量
906
审稿时长
1 months
期刊介绍: Journal of Virology (JVI) explores the nature of the viruses of animals, archaea, bacteria, fungi, plants, and protozoa. We welcome papers on virion structure and assembly, viral genome replication and regulation of gene expression, genetic diversity and evolution, virus-cell interactions, cellular responses to infection, transformation and oncogenesis, gene delivery, viral pathogenesis and immunity, and vaccines and antiviral agents.
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