论文标题
疫苗接种形状SARS-COV-2的进化轨迹
Vaccination shapes evolutionary trajectories of SARS-CoV-2
论文作者
论文摘要
SARS-COV-2病毒的大规模演变已由遗传进化枝的快速转移。新的变体显示出内在的变化,尤其提高了传播性以及抗原变化,从而减少了先前感染或疫苗接种引起的跨免疫力。这种功能变化如何塑造全局进化动力学尚不清楚。在这里,我们表明疫苗接种引起的选择会影响SARS-COV-2的近期抗原演化;其他相关力包括先前感染引起的内在选择和抗原选择。我们从具有内在和抗原适应性成分的适应性模型中获得这些结果。为了推断模型参数,我们结合了时间分辨序列数据,流行病学记录和跨中性化测定。该模型准确地捕获了多个地理区域中SARS-COV-2的大规模进化动力学。特别是,它量化了最近的疫苗接种和感染如何影响病毒变异之间的频移速度。我们的结果表明,可以收集及时的中和数据,以识别抗原选择的热点,并预测疫苗接种对病毒进化的影响。
The large-scale evolution of the SARS-CoV-2 virus has been marked by rapid turnover of genetic clades. New variants show intrinsic changes, notably increased transmissibility, as well as antigenic changes that reduce the cross-immunity induced by previous infections or vaccinations. How this functional variation shapes the global evolutionary dynamics has remained unclear. Here we show that selection induced by vaccination impacts on the recent antigenic evolution of SARS-CoV-2; other relevant forces include intrinsic selection and antigenic selection induced by previous infections. We obtain these results from a fitness model with intrinsic and antigenic fitness components. To infer model parameters, we combine time-resolved sequence data, epidemiological records, and cross-neutralisation assays. This model accurately captures the large-scale evolutionary dynamics of SARS-CoV-2 in multiple geographical regions. In particular, it quantifies how recent vaccinations and infections affect the speed of frequency shifts between viral variants. Our results show that timely neutralisation data can be harvested to identify hotspots of antigenic selection and to predict the impact of vaccination on viral evolution.