CHU de Quebec Hospital and Laval University, Quebec City, Quebec, Canada.
Gilead Sciences, Foster City, California, USA.
Antimicrob Agents Chemother. 2022 Jul 19;66(7):e0019822. doi: 10.1128/aac.00198-22. Epub 2022 Jun 16.
selection of remdesivir-resistant severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) revealed the emergence of a V166L substitution, located outside of the polymerase active site of the Nsp12 protein, after 9 passages of a single lineage. V166L remained the only Nsp12 substitution after 17 passages (10 μM remdesivir), conferring a 2.3-fold increase in 50% effective concentration (EC). When V166L was introduced into a recombinant SARS-CoV-2 virus, a 1.5-fold increase in EC was observed, indicating a high barrier to remdesivir resistance.
耐瑞德西韦的严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的选择揭示了 Nsp12 蛋白聚合酶活性位点以外的 V166L 取代的出现,这是在单个谱系中经过 9 次传代后发生的。在 17 次传代(10μM 瑞德西韦)后,V166L 仍然是唯一的 Nsp12 取代,导致 50%有效浓度(EC)增加了 2.3 倍。当 V166L 被引入重组 SARS-CoV-2 病毒时,EC 增加了 1.5 倍,表明瑞德西韦耐药性的高屏障。