Braun Katarina M, Moreno Gage K, Halfmann Peter J, Hodcroft Emma B, Baker David A, Boehm Emma C, Weiler Andrea M, Haj Amelia K, Hatta Masato, Chiba Shiho, Maemura Tadashi, Kawaoka Yoshihiro, Koelle Katia, O'Connor David H, Friedrich Thomas C
Department of Pathobiological Sciences, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
Department of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
PLoS Pathog. 2021 Feb 26;17(2):e1009373. doi: 10.1371/journal.ppat.1009373. eCollection 2021 Feb.
The evolutionary mechanisms by which SARS-CoV-2 viruses adapt to mammalian hosts and, potentially, undergo antigenic evolution depend on the ways genetic variation is generated and selected within and between individual hosts. Using domestic cats as a model, we show that SARS-CoV-2 consensus sequences remain largely unchanged over time within hosts, while dynamic sub-consensus diversity reveals processes of genetic drift and weak purifying selection. We further identify a notable variant at amino acid position 655 in Spike (H655Y), which was previously shown to confer escape from human monoclonal antibodies. This variant arises rapidly and persists at intermediate frequencies in index cats. It also becomes fixed following transmission in two of three pairs. These dynamics suggest this site may be under positive selection in this system and illustrate how a variant can quickly arise and become fixed in parallel across multiple transmission pairs. Transmission of SARS-CoV-2 in cats involved a narrow bottleneck, with new infections founded by fewer than ten viruses. In RNA virus evolution, stochastic processes like narrow transmission bottlenecks and genetic drift typically act to constrain the overall pace of adaptive evolution. Our data suggest that here, positive selection in index cats followed by a narrow transmission bottleneck may have instead accelerated the fixation of S H655Y, a potentially beneficial SARS-CoV-2 variant. Overall, our study suggests species- and context-specific adaptations are likely to continue to emerge. This underscores the importance of continued genomic surveillance for new SARS-CoV-2 variants as well as heightened scrutiny for signatures of SARS-CoV-2 positive selection in humans and mammalian model systems.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)病毒适应哺乳动物宿主并可能经历抗原进化的进化机制,取决于个体宿主内部以及个体宿主之间遗传变异的产生和选择方式。以家猫为模型,我们发现SARS-CoV-2的共有序列在宿主内随时间基本保持不变,而动态的亚共有序列多样性揭示了遗传漂变和弱纯化选择的过程。我们进一步在刺突蛋白的第655位氨基酸处(H655Y)鉴定出一个显著变异体,该变异体先前已被证明可逃避人类单克隆抗体。这个变异体在指数猫中迅速出现并以中等频率持续存在。在三对猫中的两对中,它在传播后也变得固定。这些动态变化表明该位点在这个系统中可能处于正选择之下,并说明了一个变异体如何能在多个传播对中迅速出现并同时固定下来获得。SARS-CoV-2在猫中的传播涉及一个狭窄的瓶颈,新感染由少于十种病毒引发。在RNA病毒进化中,像狭窄的传播瓶颈和遗传漂变这样的随机过程通常会限制适应性进化的总体速度。我们的数据表明,在这里,指数猫中的正选择随后是一个狭窄的传播瓶颈,反而可能加速了S H655Y的固定,这是一个潜在有益的SARS-CoV-2变异体。总体而言,我们的研究表明物种特异性和背景特异性的适应性可能会继续出现。这凸显了持续进行基因组监测以发现新的SARS-CoV-2变异体的重要性,以及加强对人类和哺乳动物模型系统中SARS-CoV-2正选择特征的审查的重要性。