Emergence of a putative novel SARS-CoV-2 P.X lineage harboring N234P and E471Q spike protein mutations in Southern Brazil

Mariana Soares da Silva,Juliana Schons Gularte,Meriane Demoliner,Alana Witt Hansen,Fágner Henrique Heldt,Micheli Filippi, Cristiane Borba Luckmann,Flávio Silveira,Vyctoria Malayhka de Abreu Góes Pereira, Rodrigo de Almeida Vaucher,Victor dos Santos Barboza,Janice Luehring Giongo, Raquel Borba Rosa, Evelise Tarouco da Rocha, Bruno Kilpp Goulart, Fernanda dos Santos Fernandes, Juliana Maciel Pinto, Leandro Pergher Bolzan, Marta Maria Medeiros Frescura Duarte,Matheus Nunes Weber,Paula Rodrigues de Almeida,Juliane Deise Fleck,Fernando Rosado Spilki

Research Square (Research Square)(2021)

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摘要
Abstract Novel SARS-CoV-2 lineages are constantly reported worldwide, raising concerns about transmissibility, virulence, immune response and vaccine/antigenic escape. Variants of concern (VOCs), as B.1.1.7 (Alpha), B.1.351 (Beta), P.1 (Gamma) and B.1.617.2 (Delta), caused epidemic outbreaks due their higher potential of transmissibility when compared with earlier waves of SARS-CoV-2 in 2019. B.1.1.28 lineage has been evolving in Brazil since February 2020 and originated P.1 (VOC), P.2 (VOI) and other P.Xs proposed as new variants. This lineage harbors specific defining mutations including two non-synonymous substitutions in the Spike (S) protein (D614G and V1176F). In this study, employing variant calling analysis on FASTQ reads and phylogenetic inference, we report a potentially new SARS-CoV-2 P.X variant. Variant calling mutational profile was investigated and presented additionally non-synonymous mutations when compared to B.1.1.28, including N234P and E471Q in S protein. Further studies are required to understand the spread of P.X variant and its potential effects on transmissibility and immune escape.
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spike protein mutations,n234p,sars-cov
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