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德尔塔毒株刺突蛋白P681R突变增强了严重急性呼吸综合征冠状病毒2相对于阿尔法毒株的适应性。

Delta spike P681R mutation enhances SARS-CoV-2 fitness over Alpha variant.

作者信息

Liu Yang, Liu Jianying, Johnson Bryan A, Xia Hongjie, Ku Zhiqiang, Schindewolf Craig, Widen Steven G, An Zhiqiang, Weaver Scott C, Menachery Vineet D, Xie Xuping, Shi Pei-Yong

机构信息

Department of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston TX, USA.

Institute for Human Infections and Immunity, University of Texas Medical Branch, Galveston TX, USA.

出版信息

bioRxiv. 2021 Sep 5:2021.08.12.456173. doi: 10.1101/2021.08.12.456173.

Abstract

SARS-CoV-2 Delta variant has rapidly replaced the Alpha variant around the world. The mechanism that drives this global replacement has not been defined. Here we report that Delta spike mutation P681R plays a key role in the Alpha-to-Delta variant replacement. In a replication competition assay, Delta SARS-CoV-2 efficiently outcompeted the Alpha variant in human lung epithelial cells and primary human airway tissues. Delta SARS-CoV-2 bearing the Alpha-spike glycoprotein replicated less efficiently than the wild-type Delta variant, suggesting the importance of Delta spike in enhancing viral replication. The Delta spike has accumulated mutation P681R located at a furin cleavage site that separates the spike 1 (S1) and S2 subunits. Reverting the P681R mutation to wild-type P681 significantly reduced the replication of Delta variant, to a level lower than the Alpha variant. Mechanistically, the Delta P681R mutation enhanced the cleavage of the full-length spike to S1 and S2, leading to increased infection via cell surface entry. In contrast, the Alpha spike also has a mutation at the same amino acid (P681H), but the spike cleavage from purified Alpha virions was reduced compared to the Delta spike. Collectively, our results indicate P681R as a key mutation in enhancing Delta variant replication via increased S1/S2 cleavage. Spike mutations that potentially affect furin cleavage efficiency must be closely monitored for future variant surveillance.

摘要

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的德尔塔变异株已在全球迅速取代了阿尔法变异株。驱动这种全球范围内变异株取代的机制尚未明确。在此,我们报告德尔塔刺突蛋白突变P681R在阿尔法变异株向德尔塔变异株的取代过程中起关键作用。在复制竞争试验中,德尔塔SARS-CoV-2在人肺上皮细胞和原代人气道组织中有效胜过阿尔法变异株。携带阿尔法刺突糖蛋白的德尔塔SARS-CoV-2复制效率低于野生型德尔塔变异株,这表明德尔塔刺突蛋白在增强病毒复制方面的重要性。德尔塔刺突蛋白在位于分隔刺突1(S1)和S2亚基的弗林蛋白酶切割位点处积累了P681R突变。将P681R突变回复为野生型P681可显著降低德尔塔变异株的复制,使其低于阿尔法变异株的水平。从机制上讲,德尔塔P681R突变增强了全长刺突蛋白向S1和S2的切割,导致通过细胞表面进入的感染增加。相比之下,阿尔法刺突蛋白在相同氨基酸位置也有一个突变(P681H),但与德尔塔刺突蛋白相比,纯化的阿尔法病毒粒子的刺突蛋白切割减少。总体而言,我们的结果表明P681R是通过增加S1/S2切割来增强德尔塔变异株复制的关键突变。对于未来的变异株监测,必须密切关注可能影响弗林蛋白酶切割效率的刺突蛋白突变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f5e/8424650/86f7f821b747/nihpp-2021.08.12.456173v3-f0002.jpg

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