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广谱抗猫、雪貂和水貂冠状病毒的蛋白酶抑制剂。

Protease inhibitors broadly effective against feline, ferret and mink coronaviruses.

机构信息

Department of Diagnostic Medicine and Pathobiology, College of Veterinary Medicine, Kansas State University, Manhattan, KS, USA.

Department of Chemistry, Wichita State University, Wichita, KS, USA.

出版信息

Antiviral Res. 2018 Dec;160:79-86. doi: 10.1016/j.antiviral.2018.10.015. Epub 2018 Oct 19.

Abstract

Ferret and mink coronaviruses typically cause catarrhal diarrhea in ferrets and minks, respectively. In recent years, however, systemic fatal coronavirus infection has emerged in ferrets, which resembles feline infectious peritonitis (FIP) in cats. FIP is a highly fatal systemic disease caused by a virulent feline coronavirus infection in cats. Despite the importance of coronavirus infections in these animals, there are no effective commercial vaccines or antiviral drugs available for these infections. We have previously reported the efficacy of a protease inhibitor in cats with FIP, demonstrating that a virally encoded 3C-like protease (3CLpro) is a valid target for antiviral drug development for coronavirus infections. In this study, we extended our previous work on coronavirus inhibitors and investigated the structure-activity relationships of a focused library of protease inhibitors for ferret and mink 3CLpro. Using the fluorescence resonance energy transfer assay, we identified potent inhibitors broadly effective against feline, ferret and mink coronavirus 3CLpro. Multiple amino acid sequence analysis and modelling of 3CLpro of ferret and mink coronaviruses were conducted to probe the structural basis for these findings. The results of this study provide support for further research to develop broad-spectrum antiviral agents for multiple coronavirus infections. To the best of our knowledge, this is the first report on small molecule inhibitors of ferret and mink coronaviruses.

摘要

雪貂和水貂冠状病毒通常分别导致雪貂和水貂出现卡他性腹泻。然而,近年来,雪貂中出现了系统性致命冠状病毒感染,类似于猫传染性腹膜炎(FIP)。FIP 是一种由猫体内高致病性猫冠状病毒感染引起的高度致命的系统性疾病。尽管这些动物的冠状病毒感染非常重要,但目前尚无针对这些感染的有效商业疫苗或抗病毒药物。我们之前曾报道过蛋白酶抑制剂在 FIP 猫中的疗效,证明病毒编码的 3C 样蛋白酶(3CLpro)是开发冠状病毒感染抗病毒药物的有效靶点。在这项研究中,我们扩展了之前对冠状病毒抑制剂的研究,并研究了针对雪貂和水貂 3CLpro 的经过优化的蛋白酶抑制剂文库的结构-活性关系。使用荧光共振能量转移测定法,我们鉴定出了对猫、雪貂和水貂冠状病毒 3CLpro 均具有广泛抑制作用的有效抑制剂。对雪貂和水貂冠状病毒 3CLpro 的多种氨基酸序列分析和建模,对这些发现的结构基础进行了探究。这项研究的结果为进一步开发针对多种冠状病毒感染的广谱抗病毒药物提供了支持。据我们所知,这是首次报道针对雪貂和水貂冠状病毒的小分子抑制剂。

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