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一种抑制甲型流感病毒核蛋白寡聚化的喹喔啉酮化合物可防止逃逸突变株的选择。

A Quinolinone Compound Inhibiting the Oligomerization of Nucleoprotein of Influenza A Virus Prevents the Selection of Escape Mutants.

机构信息

Department of Molecular Microbiology and Immunology, Graduate School of Biomedical Sciences, Nagasaki University, 1-12-4 Sakamoto, Nagasaki 852-8523, Japan.

Department of Lifestyle Design, Faculty of Human Ecology, Yasuda Women's University, 6-13-1 Yasuhigashi, Asaminami ward, Hiroshima 731-0153, Japan.

出版信息

Viruses. 2020 Mar 19;12(3):337. doi: 10.3390/v12030337.

Abstract

The emergence of resistance to currently available anti-influenza drugs has heightened the need for antivirals with novel mechanisms of action. The influenza A virus (IAV) nucleoprotein (NP) is highly conserved and essential for the formation of viral ribonucleoprotein (vRNP), which serves as the template for replication and transcription. Recently, using in silico screening, we identified an antiviral compound designated NUD-1 (a 4-hydroxyquinolinone derivative) as a potential inhibitor of NP. In this study, we further analyzed the interaction between NUD-1 and NP and found that the compound interferes with the oligomerization of NP, which is required for vRNP formation, leading to the suppression of viral transcription, protein synthesis, and nuclear export of NP. We further assessed the selection of resistant variants by serially passaging a clinical isolate of the 2009 H1N1 pandemic influenza virus in the presence of NUD-1 or oseltamivir. NUD-1 did not select for resistant variants after nine passages, whereas oseltamivir selected for resistant variants after five passages. Our data demonstrate that NUD-1 interferes with the oligomerization of NP and less likely induces drug-resistant variants than oseltamivir; hence, it is a potential lead compound for the development of novel anti-influenza drugs.

摘要

目前可用的抗流感药物出现耐药性,这使得人们更加需要具有新型作用机制的抗病毒药物。甲型流感病毒(IAV)核蛋白(NP)高度保守,是形成病毒核糖核蛋白(vRNP)所必需的,vRNP 是复制和转录的模板。最近,我们通过计算机筛选,鉴定出一种名为 NUD-1(一种 4-羟基喹啉酮衍生物)的抗病毒化合物,它可能是 NP 的抑制剂。在这项研究中,我们进一步分析了 NUD-1 与 NP 之间的相互作用,发现该化合物干扰 NP 的寡聚化,这是 vRNP 形成所必需的,从而抑制病毒转录、蛋白合成和 NP 的核输出。我们进一步评估了在 NUD-1 或奥司他韦存在的情况下,连续传代筛选 2009 年 H1N1 大流行流感病毒临床分离株的耐药变异选择情况。经过 9 次传代,NUD-1 未选择出耐药变异株,而奥司他韦在 5 次传代后选择出耐药变异株。我们的数据表明,NUD-1 干扰 NP 的寡聚化,比奥司他韦更不容易诱导耐药变异株;因此,它是开发新型抗流感药物的潜在先导化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c70/7150793/05776e5e8ee2/viruses-12-00337-g001a.jpg

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