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SARS-Cov-2's variants of concern: a brief characterization

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dc.contributor.author Scovino, Aline Miranda
dc.contributor.author Dahab, Elizabeth Chen
dc.contributor.author Vieira, Gustavo Fioravanti
dc.contributor.author Freire-de-Lima, Leonardo
dc.contributor.author Freire-de-Lima, Celio Geraldo
dc.contributor.author Morrot, Alexandre
dc.date.accessioned 2022-10-10T16:57:40Z
dc.date.available 2022-10-10T16:57:40Z
dc.date.issued 2022
dc.identifier.citation SCOVINO, A. M. et al. SARS-CoV-2?s Variants of Concern: A Brief Characterization. Frontiers in Immunology, v. 13, p. 1, 2022. Disponível em: https://www.frontiersin.org/articles/10.3389/fimmu.2022.834098/full. Acesso em: 05 out. 2022. pt_BR
dc.identifier.uri http://hdl.handle.net/11690/3349
dc.description.abstract The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) disclose the variants of concern (VOC) including Alpha (B.1.1.7), Beta (B.1.351), Gamma (P1), Delta (B.1.617.2), and Omicron (B.1.1.529). Its spike protein (S) present on the surface of the virus is recognized by the host cell receptor, the angiotensin-2 converting enzyme (ACE2) which promotes their entry into the cell. The mutations presented by VOCs are found in RBD and the N-terminal region of S protein. Therefore, mutations occurring in RBD can modify the biological and immunogenic characteristics of the virus, such as modifying the spike affinity for ACE2, increasing the virus transmissibility, or conferring the ability to escape the immune responses. The raise of a potential new SARS-CoV-2 variant capable of evading the host defenses at the same time maintaining its fitness justifies the importance of continued genetic monitoring of the pandemic coronavirus. pt_BR
dc.language.iso en_US pt_BR
dc.publisher Frontiers pt_BR
dc.rights Open Access en_US
dc.subject COVID-19 pt_BR
dc.subject SARS-CoV-2 pt_BR
dc.subject COVID-19 vaccination pt_BR
dc.subject viral immune escape pt_BR
dc.subject SARS-COV-2 variants pt_BR
dc.title SARS-Cov-2's variants of concern: a brief characterization pt_BR
dc.type Artigo pt_BR


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