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严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)德尔塔变异株刺突蛋白增强病毒融合性和炎性细胞因子产生。

SARS-CoV-2 Delta spike protein enhances the viral fusogenicity and inflammatory cytokine production.

作者信息

Ao Zhujun, Ouyang Maggie Jing, Olukitibi Titus Abiola, Yao Xiaojian

机构信息

Laboratory of Molecular Human Retrovirology, Department of Medical Microbiology, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada.

出版信息

iScience. 2022 Aug 19;25(8):104759. doi: 10.1016/j.isci.2022.104759. Epub 2022 Jul 14.

Abstract

The Delta variant had spread globally in 2021 and caused more serious disease than the original virus and Omicron variant. In this study, we investigated several virological features of Delta spike protein (SP), including protein maturation, its impact on viral entry of pseudovirus and cell-cell fusion, and its induction of inflammatory cytokine production in human macrophages and dendritic cells. The results showed that SPΔC exhibited enhanced S1/S2 cleavage in cells and pseudotyped virus-like particles (PVLPs). Further, SPΔC elevated pseudovirus entry in human lung cell lines and significantly enhanced syncytia formation. Furthermore, we revealed that SPΔC-PVLPs had stronger effects on stimulating NF-κB and AP-1 signaling in human monocytic THP1 cells and induced significantly higher levels of proinflammatory cytokine, such as TNF-α, IL-1β, and IL-6, released from human macrophages and dendritic cells. Overall, these studies provide evidence to support the important role of SPΔC during virus infection, transmission, and pathogenesis.

摘要

德尔塔变异株在2021年已在全球传播,且比原始病毒和奥密克戎变异株引发更严重的疾病。在本研究中,我们调查了德尔塔刺突蛋白(SP)的几个病毒学特征,包括蛋白成熟、其对假病毒进入和细胞间融合的影响,以及其在人类巨噬细胞和树突状细胞中诱导炎性细胞因子产生的情况。结果显示,SPΔC在细胞和假型病毒样颗粒(PVLPs)中表现出增强的S1/S2裂解。此外,SPΔC提高了假病毒在人肺细胞系中的进入率,并显著增强了合胞体形成。此外,我们发现SPΔC-PVLPs对刺激人单核细胞THP1细胞中的NF-κB和AP-1信号有更强的作用,并诱导人巨噬细胞和树突状细胞释放显著更高水平的促炎细胞因子,如TNF-α、IL-1β和IL-6。总体而言,这些研究提供了证据,支持SPΔC在病毒感染、传播和发病机制中的重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fcc/9356081/61c3d808fc65/fx1.jpg

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