Ormond Louise, Liu Ping, Matuszewski Sebastian, Renzette Nicholas, Bank Claudia, Zeldovich Konstantin, Bolon Daniel N, Kowalik Timothy F, Finberg Robert W, Jensen Jeffrey D, Wang Jennifer P
École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
Swiss Institute of Bioinformatics (SIB), Lausanne, Switzerland.
Genome Biol Evol. 2017 Jul 1;9(7):1913-1924. doi: 10.1093/gbe/evx138.
Influenza virus inflicts a heavy death toll annually and resistance to existing antiviral drugs has generated interest in the development of agents with novel mechanisms of action. Favipiravir is an antiviral drug that acts by increasing the genome-wide mutation rate of influenza A virus (IAV). Potential synergistic benefits of combining oseltamivir and favipiravir have been demonstrated in animal models of influenza, but the population-level effects of combining the drugs are unknown. In order to elucidate the underlying evolutionary processes at play, we performed genome-wide sequencing of IAV experimental populations subjected to serial passaging in vitro under a combined protocol of oseltamivir and favipiravir. We describe the interplay between mutation, selection, and genetic drift that ultimately culminates in population extinction. In particular, selective sweeps around oseltamivir resistance mutations reduce genome-wide variation while deleterious mutations hitchhike to fixation given the increased mutational load generated by favipiravir. This latter effect reduces viral fitness and accelerates extinction compared with IAV populations treated with favipiravir alone, but risks spreading both established and newly emerging mutations, including possible drug resistance mutations, if transmission occurs before the viral populations are eradicated.
流感病毒每年造成惨重的死亡人数,并且对现有抗病毒药物的耐药性引发了人们对开发具有新作用机制药物的兴趣。法匹拉韦是一种抗病毒药物,其作用机制是提高甲型流感病毒(IAV)的全基因组突变率。在流感动物模型中已证明,联合使用奥司他韦和法匹拉韦具有潜在的协同益处,但联合用药在人群层面的效果尚不清楚。为了阐明其中潜在的进化过程,我们对在奥司他韦和法匹拉韦联合用药方案下进行体外连续传代的IAV实验群体进行了全基因组测序。我们描述了突变、选择和遗传漂变之间的相互作用,这些相互作用最终导致群体灭绝。特别是,围绕奥司他韦耐药突变的选择性清除减少了全基因组变异,而有害突变由于法匹拉韦产生的突变负荷增加而搭便车固定下来。与单独使用法匹拉韦治疗的IAV群体相比,后一种效应降低了病毒适应性并加速了灭绝,但如果在病毒群体被根除之前发生传播,则有传播已有的和新出现的突变(包括可能的耐药突变)的风险。