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ACE2 表达中的遗传变异性对 SARS-CoV-2 刺突 D614G 突变进化动态的影响。

Impact of Genetic Variability in ACE2 Expression on the Evolutionary Dynamics of SARS-CoV-2 Spike D614G Mutation.

机构信息

Model Development Section, Basic Research Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702, USA.

Graduate Institute of Natural Products, College of Pharmacy, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.

出版信息

Genes (Basel). 2020 Dec 24;12(1):16. doi: 10.3390/genes12010016.

Abstract

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike (S) glycoprotein D614G mutation became the predominant globally circulating variant after its emergence in the early coronavirus disease 2019 (COVID-19) pandemic. Studies showed that this mutation results in an open conformation of the S glycoprotein receptor-binding domain (RBD), and increased angiotensin 1-converting enzyme 2 (ACE2) binding and fusion, which result in an increase in SARS-CoV-2 transmissibility and infectivity. Dynamic tracking of SARS-CoV-2 showed that the D614G variant became predominant after emergence in Europe and North America, but not in China. The current absence of selective pressures from antiviral treatment suggests that the driving force for viral evolution could be variations in human population genetics. Results show that ACE2 expression is higher in Asian populations than that in European, North American, and African populations. This supports the idea that lower ACE2 expression is a driving force in the positive selection for the D614G mutation. This study suggests that the dynamics of the SARS-CoV-2 D614G mutation during the early-to-mid pandemic is associated with enhanced transmission efficiency in populations with lower ACE2 expression. Understanding the role that human genetic diversity plays in the adaptive evolution of SARS-CoV-2 may have an important impact on public health and measures to control the pandemic.

摘要

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的刺突(S)糖蛋白 D614G 突变,在新冠肺炎(COVID-19)大流行早期出现后,成为全球主要流行的变异株。研究表明,这种突变导致 S 糖蛋白受体结合域(RBD)呈开放构象,增加血管紧张素转化酶 1(ACE2)的结合和融合,从而导致 SARS-CoV-2 的传染性和感染力增加。对 SARS-CoV-2 的动态跟踪表明,该变异株在欧洲和北美出现后成为主要流行株,但在中国并非如此。目前抗病毒治疗没有选择压力,这表明病毒进化的驱动力可能是人类群体遗传学的变异。结果表明,ACE2 的表达在亚洲人群中高于欧洲、北美和非洲人群。这支持了 ACE2 表达水平较低是 D614G 突变正选择的驱动力的观点。本研究表明,SARS-CoV-2 D614G 突变在大流行早期到中期的动态变化与 ACE2 表达水平较低的人群中传播效率的提高有关。了解人类遗传多样性在 SARS-CoV-2 的适应性进化中所起的作用,可能对公共卫生和控制大流行的措施有重要影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b0c/7824201/6e716630ed5a/genes-12-00016-g001.jpg

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