Division of Experimental and Clinical Research, Vetsuisse Faculty, University of Bern, CH-3012 Bern, Switzerland.
Institute of Chemistry and Biotechnology, Center for Organic and Medicinal Chemistry, Zurich University of Applied Sciences (ZHAW), CH-8820 Wädenswil, Switzerland.
Viruses. 2021 Jan 18;13(1):128. doi: 10.3390/v13010128.
Canine distemper virus (CDV), a close relative of the human pathogen measles virus (MeV), is an enveloped, negative sense RNA virus that belongs to the genus and causes severe diseases in dogs and other carnivores. Although the vaccination is available as a preventive measure against the disease, the occasional vaccination failure highlights the importance of therapeutic alternatives such as antivirals against CDV. The morbilliviral cell entry system relies on two interacting envelope glycoproteins: the attachment (H) and fusion (F) proteins. Here, to potentially discover novel entry inhibitors targeting CDV H, F and/or the cognate receptor: signaling lymphocyte activation molecule (SLAM) proteins, we designed a quantitative cell-based fusion assay that matched high-throughput screening (HTS) settings. By screening two libraries of small molecule compounds, we successfully identified two membrane fusion inhibitors (F2736-3056 and F2261-0043). Although both inhibitors exhibited similarities in structure and potency with the small molecule compound 3G (an AS-48 class morbilliviral F-protein inhibitor), F2736-3056 displayed improved efficacy in blocking fusion activity when a 3G-escape variant was employed. Altogether, we present a cell-based fusion assay that can be utilized not only to discover antiviral agents against CDV but also to dissect the mechanism of morbilliviral-mediated cell-binding and cell-to-cell fusion activity.
犬瘟热病毒(CDV)是麻疹病毒(MeV)的近亲,属于副黏病毒科,是一种有包膜的负义 RNA 病毒,可引起犬和其他食肉动物的严重疾病。尽管可以接种疫苗作为预防该病的措施,但偶尔的疫苗接种失败凸显了开发针对 CDV 的抗病毒治疗药物等替代疗法的重要性。副黏病毒的细胞进入系统依赖于两种相互作用的包膜糖蛋白:附着(H)和融合(F)蛋白。在这里,为了有可能发现针对 CDV H、F 和/或同源受体:信号淋巴细胞激活分子(SLAM)蛋白的新型进入抑制剂,我们设计了一种定量细胞融合测定法,以适应高通量筛选(HTS)设置。通过筛选两种小分子化合物文库,我们成功鉴定出两种膜融合抑制剂(F2736-3056 和 F2261-0043)。尽管这两种抑制剂在结构和效力上都与小分子化合物 3G(一种 AS-48 类副黏病毒 F 蛋白抑制剂)相似,但当使用 3G 逃逸变异体时,F2736-3056 显示出更好的阻断融合活性的效果。总之,我们提出了一种基于细胞的融合测定法,不仅可以用于发现针对 CDV 的抗病毒药物,还可以用于剖析副黏病毒介导的细胞结合和细胞间融合活性的机制。