Division of Infectious Diseases, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Division of Infectious Diseases, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Cell Host Microbe. 2021 Jan 13;29(1):23-31.e4. doi: 10.1016/j.chom.2020.11.012. Epub 2020 Dec 1.
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein acquired a D614G mutation early in the pandemic that confers greater infectivity and is now the globally dominant form. To determine whether D614G might also mediate neutralization escape that could compromise vaccine efficacy, sera from spike-immunized mice, nonhuman primates, and humans were evaluated for neutralization of pseudoviruses bearing either D614 or G614 spike. In all cases, the G614 pseudovirus was moderately more susceptible to neutralization. The G614 pseudovirus also was more susceptible to neutralization by receptor-binding domain (RBD) monoclonal antibodies and convalescent sera from people infected with either form of the virus. Negative stain electron microscopy revealed a higher percentage of the 1-RBD "up" conformation in the G614 spike, suggesting increased epitope exposure as a mechanism of enhanced vulnerability to neutralization. Based on these findings, the D614G mutation is not expected to be an obstacle for current vaccine development.
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的刺突蛋白在大流行早期发生了 D614G 突变,从而获得了更高的传染性,并且现在是全球主要流行形式。为了确定 D614G 是否也介导中和逃逸,从而影响疫苗的效果,我们评估了针对携带 D614 或 G614 刺突的假病毒的 Spike 免疫的小鼠、非人类灵长类动物和人类血清的中和作用。在所有情况下,G614 假病毒对中和作用的敏感性都略有增加。G614 假病毒也更容易被受体结合域(RBD)单克隆抗体和感染了该病毒两种形式的人的恢复期血清中和。负染电子显微镜显示,G614 刺突中的 1-RBD“朝上”构象的比例更高,表明增加了表位暴露,这是增加对中和作用易感性的一种机制。基于这些发现,预计 D614G 突变不会成为当前疫苗开发的障碍。