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.
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.
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DOI:
10.1093/ve/veab069
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发表时间:
2021
期刊:
影响因子:
5.3
通讯作者:
Wallau GL
中科院分区:
文献类型:
--
作者:
Resende PC;Naveca FG;Lins RD;Dezordi FZ;Ferraz MVF;Moreira EG;Coêlho DF;Motta FC;Paixão ACD;Appolinario L;Lopes RS;Mendonça ACDF;da Rocha ASB;Nascimento V;Souza V;Silva G;Nascimento F;Neto LGL;da Silva FV;Riediger I;Debur MDC;Leite AB;Mattos T;da Costa CF;Pereira FM;Dos Santos CA;Rovaris DB;Fernandes SB;Abbud A;Sacchi C;Khouri R;Bernardes AFL;Delatorre E;Gräf T;Siqueira MM;Bello G;Wallau GL
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.
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DOI:
10.1093/bioinformatics/btx346
发表时间:
2017-10-01
期刊:
Bioinformatics (Oxford, England)
影响因子:
--
作者:
Gel B;Serra E
通讯作者:
Serra E
DOI:
10.1126/science.abi6226
发表时间:
2021-08-06
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Gobeil SM;Janowska K;McDowell S;Mansouri K;Parks R;Stalls V;Kopp MF;Manne K;Li D;Wiehe K;Saunders KO;Edwards RJ;Korber B;Haynes BF;Henderson R;Acharya P
通讯作者:
Acharya P
影响因子:
64.8
作者:
Kemp SA;Collier DA;Datir RP;Ferreira IATM;Gayed S;Jahun A;Hosmillo M;Rees-Spear C;Mlcochova P;Lumb IU;Roberts DJ;Chandra A;Temperton N;CITIID-NIHR BioResource COVID-19 Collaboration;COVID-19 Genomics UK (COG-UK) Consortium;Sharrocks K;Blane E;Modis Y;Leigh KE;Briggs JAG;van Gils MJ;Smith KGC;Bradley JR;Smith C;Doffinger R;Ceron-Gutierrez L;Barcenas-Morales G;Pollock DD;Goldstein RA;Smielewska A;Skittrall JP;Gouliouris T;Goodfellow IG;Gkrania-Klotsas E;Illingworth CJR;McCoy LE;Gupta RK
通讯作者:
Gupta RK
影响因子:
48
作者:
Kalyaanamoorthy S;Minh BQ;Wong TKF;von Haeseler A;Jermiin LS
通讯作者:
Jermiin LS
影响因子:
56.9
作者:
Baum, Alina;Fulton, Benjamin O.;Kyratsous, Christos A.
通讯作者:
Kyratsous, Christos A.