Graduate Program in Biological & Biomedical Sciences, Cornell Universitygrid.5386.8, Ithaca, New York, USA.
Department of Microbiology and Immunology, College of Veterinary Medicine, Cornell Universitygrid.5386.8, Ithaca, New York, USA.
Microbiol Spectr. 2022 Aug 31;10(4):e0151422. doi: 10.1128/spectrum.01514-22. Epub 2022 Jun 29.
Based on its predicted ability to affect transmissibility and pathogenesis, surveillance studies have highlighted the role of a specific mutation (P681R) in the S1/S2 furin cleavage site of the SARS-CoV-2 spike protein. Here we analyzed A.23.1, first identified in Uganda, as a P681R-containing virus several months prior to the emergence of B.1.617.2 (Delta variant). We performed assays using peptides mimicking the S1/S2 from A.23.1 and B.1.617 and observed significantly increased cleavability with furin compared to both an original B lineage (Wuhan-Hu1) and B.1.1.7 (Alpha variant). We also performed cell-cell fusion and functional infectivity assays using pseudotyped particles and observed an increase in activity for A.23.1 compared to an original B lineage spike. However, these changes in activity were not reproduced in the B lineage spike bearing only the P681R substitution. Our findings suggest that while A.23.1 has increased furin-mediated cleavage linked to the P681R substitution, this substitution needs to occur on the background of other spike protein changes to enable its functional consequences. During the course of the SARS-CoV-2 pandemic, viral variants have emerged that often contain notable mutations in the spike gene. Mutations that encode changes in the spike S1/S2 (furin) activation site have been considered especially impactful. The S1/S2 change from proline to arginine at position 681 (P681R) first emerged in the A.23.1 variant in Uganda, and subsequently occurred in the more widely transmitted Delta variant. We show that the A.23.1 spike is more readily activated by the host cell protease furin, but that this is not reproduced in an original SARS-CoV-2 spike containing the P681R mutation. Changes to the S1/S2 (furin) activation site play a role in SARS-CoV-2 infection and spread, but successful viruses combine these mutations with other less well identified changes, occurring as part of natural selection.
基于其影响传染性和发病机制的预测能力,监测研究强调了 SARS-CoV-2 刺突蛋白 S1/S2 弗林裂解位点特定突变(P681R)的作用。在这里,我们分析了 A.23.1,它首先在乌干达被发现,是一种含有 P681R 的病毒,比 B.1.617.2(Delta 变体)的出现早几个月。我们使用模拟 A.23.1 和 B.1.617 的 S1/S2 的肽进行了测定,与原始 B 谱系(武汉-Hu1)和 B.1.1.7(Alpha 变体)相比,发现与弗林的裂解能力显着增加。我们还使用假型颗粒进行了细胞-细胞融合和功能感染测定,并观察到与原始 B 谱系刺突相比,A.23.1 的活性增加。然而,在仅携带 P681R 取代的 B 谱系刺突中,并未再现这些活性变化。我们的研究结果表明,虽然 A.23.1 具有与 P681R 取代相关的增加的弗林介导的裂解,但这种取代需要在其他刺突蛋白变化的背景下发生,才能使其产生功能后果。 在 SARS-CoV-2 大流行期间,已经出现了经常在刺突基因中带有显着突变的病毒变体。编码在刺突 S1/S2(弗林)激活位点发生突变的突变被认为特别有影响。位置 681 处脯氨酸到精氨酸的 S1/S2 变化(P681R)首先出现在乌干达的 A.23.1 变体中,随后出现在传播更广泛的 Delta 变体中。我们表明,A.23.1 刺突更容易被宿主细胞蛋白酶弗林激活,但在含有 P681R 突变的原始 SARS-CoV-2 刺突中并未重现。S1/S2(弗林)激活位点的变化在 SARS-CoV-2 感染和传播中起作用,但成功的病毒将这些突变与其他不太明确的变化结合在一起,这些变化是自然选择的一部分。