WHO Collaborating Centre for Reference and Research on Influenza, VIDRL, Peter Doherty Institute for Infection and Immunity, Melbourne, VIC 3000, Australia; Biomedicine Discovery Institute & Department of Microbiology, Monash University, Victoria 3800, Australia.
WHO Collaborating Centre for Reference and Research on Influenza, VIDRL, Peter Doherty Institute for Infection and Immunity, Melbourne, VIC 3000, Australia.
Antiviral Res. 2019 Apr;164:91-96. doi: 10.1016/j.antiviral.2019.02.007. Epub 2019 Feb 13.
Baloxavir Marboxil (BXM) is an influenza polymerase inhibitor antiviral that binds to the endonuclease region in the PA subunit of influenza A and B viruses. To establish the baseline susceptibility of viruses circulating prior to licensure of BXM and to monitor for susceptibility post-BXM use, a cell culture-based focus reduction assay was developed to determine the susceptibility of 286 circulating seasonal influenza viruses, A(H1N1)pdm09, A(H3N2), B (Yamagata/Victoria) lineage viruses, including neuraminidase inhibitor (NAI) resistant viruses, to Baloxavir Acid (BXA), the active metabolic form of BXM. BXA was effective against all influenza subtypes tested with mean EC values (minimum-maximum) of 0.7 ± 0.5 nM (0.1-2.1 nM), 1.2 ± 0.6 nM (0.1-2.4), 7.2 ± 3.5 nM (0.7-14.8), and 5.8 ± 4.5 nM (1.8-15.5) obtained for A(H1N1)pdm09, A(H3N2), B(Victoria lineage), and B(Yamagata lineage) influenza viruses, respectively. Using reverse genetics, amino acid substitutions known to alter BXA susceptibility were introduced into the PA protein resulting in EC fold change increases that ranged from 2 to 65. Our study demonstrates that currently circulating viruses are susceptible to BXA and that the newly developed focus reduction assay is well suited to susceptibility monitoring in reference laboratories.
巴洛沙韦马波西酯(BXM)是一种流感聚合酶抑制剂抗病毒药物,可与甲型和乙型流感病毒的 PA 亚单位的内切酶区域结合。为了确定在 BXM 获得许可之前循环病毒的基线敏感性,并监测 BXM 使用后的敏感性,开发了一种基于细胞培养的焦点减少测定法,以确定 286 种循环季节性流感病毒、A(H1N1)pdm09、A(H3N2)、B(山形/维多利亚)谱系病毒对巴洛沙韦酸(BXA)的敏感性,BXA 是 BXM 的活性代谢形式。BXA 对所有测试的流感亚型均有效,平均 EC 值(最小值-最大值)分别为 0.7±0.5 nM(0.1-2.1 nM)、1.2±0.6 nM(0.1-2.4 nM)、7.2±3.5 nM(0.7-14.8 nM)和 5.8±4.5 nM(1.8-15.5 nM),用于 A(H1N1)pdm09、A(H3N2)、B(维多利亚谱系)和 B(山形谱系)流感病毒。通过反向遗传学,将已知可改变 BXA 敏感性的氨基酸取代引入 PA 蛋白中,导致 EC 倍增加幅范围为 2 至 65。我们的研究表明,目前循环的病毒对 BXA 敏感,并且新开发的焦点减少测定法非常适合参考实验室的敏感性监测。