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鉴定靶向流感 A 病毒 2 型血凝素的新型抑制剂。

Identification of a novel inhibitor targeting influenza A virus group 2 hemagglutinins.

机构信息

Department of Microbiology and Immunology, College of Medicine, University of Illinois at Chicago, Chicago, IL, 60612, USA.

Department of Microbiology and Immunology, College of Medicine, University of Illinois at Chicago, Chicago, IL, 60612, USA.

出版信息

Antiviral Res. 2021 Feb;186:105013. doi: 10.1016/j.antiviral.2021.105013. Epub 2021 Jan 8.

Abstract

Influenza A virus (IAV) causes seasonal epidemics and occasional but devastating pandemics, which are major public health concerns. The putative antiviral therapeutics are useful for the treatment of influenza, however, the emerging resistant strains necessitate a constant search for new drug candidates. Here we report the discovery of a novel antiviral agent, compound CBS1194, which was identified by a parallel high-throughput screening (HTS) campaign using two retroviral pseudotypes bearing H7 or H5 hemagglutinins (HAs). Subsequent analyses demonstrated that CBS1194 is specific to IAVs of group 2, while it has no effect against those of group 1. In a time-of-addition assay, CBS1194 showed a significant inhibitory effect during the early phase of viral infection. In addition, HA-mediated hemolysis can be inhibited by CBS1194 treatment, indicating that this compound may target the HA stalk region, which is responsible for membrane fusion. Escape mutant analyses and in silico docking further revealed that CBS1194 fits into a pocket near the fusion peptide, causing steric hindrance that blocks the low-pH induced rearrangement of HA. In summary, our study identifies a novel fusion inhibitor of group 2 IAVs, which has the potential as lead compound for further development.

摘要

甲型流感病毒(IAV)会引发季节性流行疾病,并偶尔导致具有毁灭性的大流行,这是重大的公共卫生关切。拟用的抗病毒疗法对流感的治疗很有用,但是,新出现的耐药株需要不断寻找新的候选药物。在这里,我们报告了一种新型抗病毒药物 CBS1194 的发现,该药物是通过使用两种带有 H7 或 H5 血凝素(HA)的逆转录病毒假型进行平行高通量筛选(HTS)发现的。随后的分析表明,CBS1194 专门针对属于 2 组的 IAV,而对属于 1 组的 IAV 没有效果。在添加时间测定中,CBS1194 在病毒感染的早期阶段表现出显著的抑制作用。此外,CBS1194 处理可抑制 HA 介导的溶血,表明该化合物可能靶向负责膜融合的 HA 茎区。逃逸突变分析和计算机对接进一步表明,CBS1194 适合融合肽附近的一个口袋中,从而造成空间位阻,阻止 HA 在低 pH 诱导下的重排。总之,我们的研究鉴定了一种新型的 2 组 IAV 融合抑制剂,具有进一步开发的潜力。

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