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Novel SARS-CoV-2 variants: the pandemics within the pandemic
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4627390
Author(s) Boehm, Erik; Kronig, Ilona; Neher, Richard A.; Eckerle, Isabella; Vetter, Pauline; Kaiser, Laurent
Author(s) at UniBasel Neher, Richard
Year 2021
Title Novel SARS-CoV-2 variants: the pandemics within the pandemic
Journal Clinical microbiology and infection
Volume 27
Number 8
Pages / Article-Number 1109-1117
Keywords B.1.1.7; B.1.351; COVID-19; Mutations; P.1; Re-infection; SARS-CoV-2; Sequencing; VOC; Variant of concern; Variants
Mesh terms Antibodies, Neutralizing, immunology; Antibodies, Viral, immunology; Brazil, epidemiology; COVID-19, epidemiology, transmission, virology; Epidemiological Monitoring; Genetic Variation; Humans; Mutation; Pandemics; SARS-CoV-2, genetics, immunology; South Africa, epidemiology; United Kingdom, epidemiology
Abstract 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.; 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.; 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.; 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.; 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.
Publisher Elsevier
ISSN/ISBN 1198-743X ; 1469-0691
edoc-URL https://edoc.unibas.ch/84935/
Full Text on edoc No
Digital Object Identifier DOI 10.1016/j.cmi.2021.05.022
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/34015535
ISI-Number 000683532300008
Document type (ISI) Journal Article, Review
 
   

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