Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA; Howard Hughes Medical Institute, Seattle, WA, USA.
Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA; Howard Hughes Medical Institute, Seattle, WA, USA.
Cell Host Microbe. 2023 Nov 8;31(11):1898-1909.e3. doi: 10.1016/j.chom.2023.09.012. Epub 2023 Oct 25.
Through antigenic evolution, viruses such as seasonal influenza evade recognition by neutralizing antibodies. This means that a person with antibodies well tuned to an initial infection will not be protected against the same virus years later and that vaccine-mediated protection will decay. To expand our understanding of which endemic human viruses evolve in this fashion, we assess adaptive evolution across the genome of 28 endemic viruses spanning a wide range of viral families and transmission modes. Surface proteins consistently show the highest rates of adaptation, and ten viruses in this panel are estimated to undergo antigenic evolution to selectively fix mutations that enable the escape of prior immunity. Thus, antibody evasion is not an uncommon evolutionary strategy among human viruses, and monitoring this evolution will inform future vaccine efforts. Additionally, by comparing overall amino acid substitution rates, we show that SARS-CoV-2 is accumulating protein-coding changes at substantially faster rates than endemic viruses.
通过抗原进化,季节性流感等病毒逃避了中和抗体的识别。这意味着,对初始感染具有良好调节作用的抗体的人,几年后不会对同一病毒产生保护作用,疫苗介导的保护作用会减弱。为了更深入地了解哪些地方性人类病毒会以这种方式进化,我们评估了跨越广泛病毒家族和传播模式的 28 种地方性病毒基因组的适应性进化。表面蛋白始终显示出最高的适应率,在该面板中的十种病毒被估计会发生抗原进化,从而选择性固定突变,使先前的免疫逃逸。因此,抗体逃避并不是人类病毒中常见的进化策略,监测这种进化将为未来的疫苗工作提供信息。此外,通过比较整体氨基酸替换率,我们表明,SARS-CoV-2 比地方性病毒更快地积累蛋白质编码变化。