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Novel SARS-CoV-2 variants: the pandemics within the pandemic

BACKGROUND: Many new variants of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have been termed variants of concern/interest (VOC/I) because of the greater risk they pose due to possible enhanced transmissibility and/or severity, immune escape, diagnostic and/or treatment failure,...

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Autores principales: Boehm, Erik, Kronig, Ilona, Neher, Richard A., Eckerle, Isabella, Vetter, Pauline, Kaiser, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8127517/
https://www.ncbi.nlm.nih.gov/pubmed/34015535
http://dx.doi.org/10.1016/j.cmi.2021.05.022
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author Boehm, Erik
Kronig, Ilona
Neher, Richard A.
Eckerle, Isabella
Vetter, Pauline
Kaiser, Laurent
author_facet Boehm, Erik
Kronig, Ilona
Neher, Richard A.
Eckerle, Isabella
Vetter, Pauline
Kaiser, Laurent
author_sort Boehm, Erik
collection PubMed
description BACKGROUND: Many new variants of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have been termed variants of concern/interest (VOC/I) because of the greater risk they pose due to possible enhanced transmissibility and/or severity, immune escape, diagnostic and/or treatment failure, and reduced vaccine efficacy. AIMS: We sought to review the current knowledge of emerging SARS-CoV-2 variants, particularly those deemed VOC/Is: B.1.351, B.1.1.7, and P.1. SOURCES: MEDLINE and BioRxiv databases, as well as the grey literature, were searched for reports of SARS-CoV-2 variants since November 2020. Relevant articles and their references were screened. CONTENT: Mutations on the spike protein in particular may affect both affinity for the SARS-CoV-2 cell receptor ACEII and antibody binding. These VOC/Is often share similar mutation sets. The N501Y mutation is shared by the three main VOCs: B.1.1.7, first identified in the United Kingdom, P.1, originating from Brazil, and B.1.351, first described in South Africa. This mutation likely increases transmissibility by increasing affinity for ACEII. The B.1.351 and P.1 variants also display the E484K mutation which decreases binding of neutralizing antibodies, leading to partial immune escape; this favours reinfections, and decreases the in vitro efficacy of some antibody therapies or vaccines. Those mutations may also have phenotypical repercussions of greater severity. Furthermore, the accumulation of mutations poses a diagnostic risk (lowered when using multiplex assays), as seen for some assays targeting the S gene. With ongoing surveillance, many new VOC/Is have been identified. The emergence of the E484K mutation independently in different parts of the globe may reflect the adaptation of SARS-CoV-2 to humans against a background of increasing immunity. IMPLICATIONS: These VOC/Is are increasing in frequency globally and pose challenges to any herd immunity approach to managing the pandemic. While vaccination is ongoing, vaccine updates may be prudent. The virus continues to adapt to transmission in humans, and further divergence from the initial Wuhan sequences is expected.
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spelling pubmed-81275172021-05-18 Novel SARS-CoV-2 variants: the pandemics within the pandemic Boehm, Erik Kronig, Ilona Neher, Richard A. Eckerle, Isabella Vetter, Pauline Kaiser, Laurent Clin Microbiol Infect Narrative Review BACKGROUND: Many new variants of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have been termed variants of concern/interest (VOC/I) because of the greater risk they pose due to possible enhanced transmissibility and/or severity, immune escape, diagnostic and/or treatment failure, and reduced vaccine efficacy. AIMS: We sought to review the current knowledge of emerging SARS-CoV-2 variants, particularly those deemed VOC/Is: B.1.351, B.1.1.7, and P.1. SOURCES: MEDLINE and BioRxiv databases, as well as the grey literature, were searched for reports of SARS-CoV-2 variants since November 2020. Relevant articles and their references were screened. CONTENT: Mutations on the spike protein in particular may affect both affinity for the SARS-CoV-2 cell receptor ACEII and antibody binding. These VOC/Is often share similar mutation sets. The N501Y mutation is shared by the three main VOCs: B.1.1.7, first identified in the United Kingdom, P.1, originating from Brazil, and B.1.351, first described in South Africa. This mutation likely increases transmissibility by increasing affinity for ACEII. The B.1.351 and P.1 variants also display the E484K mutation which decreases binding of neutralizing antibodies, leading to partial immune escape; this favours reinfections, and decreases the in vitro efficacy of some antibody therapies or vaccines. Those mutations may also have phenotypical repercussions of greater severity. Furthermore, the accumulation of mutations poses a diagnostic risk (lowered when using multiplex assays), as seen for some assays targeting the S gene. With ongoing surveillance, many new VOC/Is have been identified. The emergence of the E484K mutation independently in different parts of the globe may reflect the adaptation of SARS-CoV-2 to humans against a background of increasing immunity. IMPLICATIONS: These VOC/Is are increasing in frequency globally and pose challenges to any herd immunity approach to managing the pandemic. While vaccination is ongoing, vaccine updates may be prudent. The virus continues to adapt to transmission in humans, and further divergence from the initial Wuhan sequences is expected. European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. 2021-08 2021-05-17 /pmc/articles/PMC8127517/ /pubmed/34015535 http://dx.doi.org/10.1016/j.cmi.2021.05.022 Text en © 2021 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Narrative Review
Boehm, Erik
Kronig, Ilona
Neher, Richard A.
Eckerle, Isabella
Vetter, Pauline
Kaiser, Laurent
Novel SARS-CoV-2 variants: the pandemics within the pandemic
title Novel SARS-CoV-2 variants: the pandemics within the pandemic
title_full Novel SARS-CoV-2 variants: the pandemics within the pandemic
title_fullStr Novel SARS-CoV-2 variants: the pandemics within the pandemic
title_full_unstemmed Novel SARS-CoV-2 variants: the pandemics within the pandemic
title_short Novel SARS-CoV-2 variants: the pandemics within the pandemic
title_sort novel sars-cov-2 variants: the pandemics within the pandemic
topic Narrative Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8127517/
https://www.ncbi.nlm.nih.gov/pubmed/34015535
http://dx.doi.org/10.1016/j.cmi.2021.05.022
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