Department of Virology, Bernhard-Nocht-Institute for Tropical Medicine, Hamburg, Germany.
KU Leuven, Rega Institute for Medical Research, Belgium.
Antiviral Res. 2020 Nov;183:104947. doi: 10.1016/j.antiviral.2020.104947. Epub 2020 Sep 24.
Several fatal bunyavirus infections lack specific treatment. Here, we show that diketo acids engage a panel of bunyavirus cap-snatching endonucleases, inhibit their catalytic activity and reduce viral replication of a taxonomic representative in vitro. Specifically, the non-salt form of L-742,001 and its derivatives exhibited EC values between 5.6 and 6.9 μM against a recombinant BUNV-mCherry virus. Structural analysis and molecular docking simulations identified traits of both the class of chemical entities and the viral target that could help the design of novel, more potent molecules for the development of pan-bunyavirus antivirals.
几种致命的布尼亚病毒感染缺乏特效治疗方法。在这里,我们发现二酮酸可与一系列布尼亚病毒帽状结构内切酶结合,抑制其催化活性,并降低代表种属的病毒在体外的复制。具体来说,非盐形式的 L-742,001 及其衍生物对重组 BUNV-mCherry 病毒的 EC 值在 5.6 和 6.9 μM 之间。结构分析和分子对接模拟确定了这一类化学实体和病毒靶标的特征,有助于设计新型、更有效的泛布尼亚病毒抗病毒药物。