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通过刺突蛋白氨基(N)末端结构域的趋同插入缺失揭示巴西SARS-CoV-2关注变异株和感兴趣变异株的持续进化。

The ongoing evolution of variants of concern and interest of SARS-CoV-2 in Brazil revealed by convergent indels in the amino (N)-terminal domain of the spike protein.

作者信息

Resende Paola Cristina, Naveca Felipe G, Lins Roberto D, Dezordi Filipe Zimmer, Ferraz Matheus V F, Moreira Emerson G, Coêlho Danilo F, Motta Fernando Couto, Paixão Anna Carolina Dias, Appolinario Luciana, Lopes Renata Serrano, Mendonça Ana Carolina da Fonseca, da Rocha Alice Sampaio Barreto, Nascimento Valdinete, Souza Victor, Silva George, Nascimento Fernanda, Neto Lidio Gonçalves Lima, da Silva Fabiano Vieira, Riediger Irina, Debur Maria do Carmo, Leite Anderson Brandao, Mattos Tirza, da Costa Cristiano Fernandes, Pereira Felicidade Mota, Dos Santos Cliomar Alves, Rovaris Darcita Buerger, Fernandes Sandra Bianchini, Abbud Adriano, Sacchi Claudio, Khouri Ricardo, Bernardes André Felipe Leal, Delatorre Edson, Gräf Tiago, Siqueira Marilda Mendonça, Bello Gonzalo, Wallau Gabriel L

机构信息

Laboratory of Respiratory Viruses and Measles (LVRS), Instituto Oswaldo Cruz, FIOCRUZ-Rio de Janeiro, Av. Brasil, 4365 - Manguinhos, Rio de Janeiro 21040-900, Brazil.

Laboratório de Ecologia de Doenças Transmissíveis na Amazônia (EDTA), Instituto Leônidas e Maria Deane, FIOCRUZ-Amazonas, Rua Teresina, 476. Adrianópolis, Manaus 69.057-070, Brazil.

出版信息

Virus Evol. 2021 Aug 14;7(2):veab069. doi: 10.1093/ve/veab069. eCollection 2021.

Abstract

Mutations at both the receptor-binding domain (RBD) and the amino (N)-terminal domain (NTD) of the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Spike (S) glycoprotein can alter its antigenicity and promote immune escape. We identified that SARS-CoV-2 lineages circulating in Brazil with mutations of concern in the RBD independently acquired convergent deletions and insertions in the NTD of the S protein, which altered the NTD antigenic-supersite and other predicted epitopes at this region. Importantly, we detected the community transmission of different P.1 lineages bearing NTD indels ∆69-70 (which can impact several SARS-CoV-2 diagnostic protocols), ∆144 and ins214ANRN, and a new VOI N.10 derived from the B.1.1.33 lineage carrying three NTD deletions (∆141-144, ∆211, and ∆256-258). These findings support that the ongoing widespread transmission of SARS-CoV-2 in Brazil generates new viral lineages that might be more resistant to antibody neutralization than parental variants of concern.

摘要

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突(S)糖蛋白的受体结合域(RBD)和氨基(N)末端域(NTD)的突变均可改变其抗原性并促进免疫逃逸。我们发现,在巴西传播的SARS-CoV-2谱系,其RBD存在值得关注的突变,这些谱系在S蛋白的NTD中独立获得了趋同的缺失和插入,这改变了NTD抗原超位点以及该区域的其他预测表位。重要的是,我们检测到了携带NTD插入缺失∆69-70(可影响多种SARS-CoV-2诊断方案)、∆144和ins214ANRN的不同P.1谱系以及源自携带三个NTD缺失(∆141-144、∆211和∆256-258)的B.1.1.33谱系的新变异株N.10的社区传播。这些发现支持,SARS-CoV-2在巴西的持续广泛传播产生了新病毒谱系,这些谱系可能比相关亲本变异株更能抵抗抗体中和作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e47a/8438916/06a6d7da063f/veab069f1.jpg

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