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S 蛋白 1/2 连接处缺失的 SARS-CoV-2 减毒株。

Attenuated SARS-CoV-2 variants with deletions at the S1/S2 junction.

机构信息

Department of Microbiology and State Key Laboratory for Emerging Infectious Diseases, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, People's Republic of China.

State Key Laboratory of Respiratory Disease, Institute of Integration of Traditional and Western Medicine, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou Medical University, Guangzhou, People's Republic of China.

出版信息

Emerg Microbes Infect. 2020 Dec;9(1):837-842. doi: 10.1080/22221751.2020.1756700.

Abstract

The emergence of SARS-CoV-2 has led to the current global coronavirus pandemic and more than one million infections since December 2019. The exact origin of SARS-CoV-2 remains elusive, but the presence of a distinct motif in the S1/S2 junction region suggests the possible acquisition of cleavage site(s) in the spike protein that promoted cross-species transmission. Through plaque purification of Vero-E6 cultured SARS-CoV-2, we found a series of variants which contain 15-30-bp deletions (Del-mut) or point mutations respectively at the S1/S2 junction. Examination of the original clinical specimen from which the isolate was derived, and 26 additional SARS-CoV-2 positive clinical specimens, failed to detect these variants. Infection of hamsters shows that one of the variants (Del-mut-1) which carries deletion of 10 amino acids (30bp) does not cause the body weight loss or more severe pathological changes in the lungs that is associated with wild type virus infection. We suggest that the unique cleavage motif promoting SARS-CoV-2 infection in humans may be under strong selective pressure, given that replication in permissive Vero-E6 cells leads to the loss of this adaptive function. It would be important to screen the prevalence of these variants in asymptomatic infected cases. The potential of the Del-mut variants as an attenuated vaccine or laboratory tool should be evaluated.

摘要

SARS-CoV-2 的出现导致了目前的全球冠状病毒大流行,自 2019 年 12 月以来已有超过 100 万人感染。SARS-CoV-2 的确切起源仍然难以捉摸,但 S1/S2 交界处存在独特的基序表明,刺突蛋白中可能获得了促进跨物种传播的切割位点。通过对 Vero-E6 培养的 SARS-CoV-2 进行噬菌斑纯化,我们发现了一系列变体,它们在 S1/S2 交界处分别含有 15-30bp 的缺失(Del-mut)或点突变。对分离株来源的原始临床标本和 26 份额外的 SARS-CoV-2 阳性临床标本进行检测,均未能检测到这些变体。仓鼠感染实验表明,其中一种变体(Del-mut-1)携带 10 个氨基酸(30bp)的缺失,不会导致体重减轻或肺部更严重的病理变化,而野生型病毒感染会导致这些变化。我们认为,在允许的 Vero-E6 细胞中复制会导致这种适应性功能丧失,因此,促进 SARS-CoV-2 感染的独特切割基序可能受到强烈的选择压力。对无症状感染病例中这些变体的流行情况进行筛查是很重要的。应该评估 Del-mut 变体作为减毒疫苗或实验室工具的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d8/7241555/4aab15a24ac6/TEMI_A_1756700_F0001_OC.jpg

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