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Emerging SARS-CoV-2 variants can potentially break set epidemiological barriers in COVID-19

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Summary: SARS-CoV-2 virus can mutate and evade immunity, with mutations like N439K conferring resistance against neutralizing monoclonal antibodies and enhancing binding affinity to hACE2 receptor. Despite similar in vitro replication fitness and clinical outcomes compared to wild type, N439K mutation highlights the importance of ongoing molecular surveillance for guiding vaccine and therapeutic development and usage.
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Rui Wang et al.

Summary: The study reveals many mutations on the RBD of the S protein, with the majority strengthening the binding between the RBD and host ACE2, indicating an evolution towards more infectious variants. Additionally, certain mutations found in different variants may weaken the binding between the RBD and antibodies, potentially compromising existing vaccines and antibody therapies. The study also identifies potential vaccine escape mutations that could pose a threat to current vaccines and antibody treatments.

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Summary: The new variants of SARS-CoV-2 are more contagious and require further investigation on their interaction with the host receptor to identify new therapeutic options. Specific mutations in the Spike glycoprotein of the new variants may play a critical role in their unique pathogenicity.

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Summary: Genetic and testing data from England indicate that the SARS-CoV-2 variant B.1.1.7 has a transmission advantage over other lineages, showing a rapid expansion during autumn 2020. Analysis of S gene target failures (SGTF) in community-based diagnostic PCR testing suggests that B.1.1.7 is more transmissible than non-variant of concern lineages and has a significant transmission advantage, with a reproduction number 50% to 100% higher. Additionally, cases of B.1.1.7 appear to include a larger share of under 20-year-olds compared to non-variant cases.

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Summary: A new variant of concern, P.1, with 17 mutations including three spike protein mutations associated with increased binding to human ACE2 receptors, emerged in Manaus, Brazil between November 2020 and January 2021. Molecular analysis suggests P.1 may be 1.7- to 2.4-fold more transmissible and that previous infection may provide 54 to 79% protection against P.1 infection compared to other lineages. Enhanced global genomic surveillance of such variants is crucial for pandemic response.

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Summary: This study systematically analyzed the binding mechanism between the spike protein of SARS-CoV-2 and the ACE2 receptor, identifying key interacting amino acids. The research confirmed key residues responsible for tight binding with ACE2 and slightly different interacting amino acids in the Alpha and Beta variants.

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Summary: The evolution of SARS-CoV-2 has been characterized by the emergence of mutations and variants that impact virus characteristics. Manufacturers are preparing for possible updates to vaccines in response to changes in the virus population, and it is crucial to monitor genetic and antigenic changes alongside experiments to understand the impacts of mutations.

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SCIENCE (2021)

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Summary: The study evaluated the relationship between Covid-19 diagnosis and the B.1.1.7 variant of concern, finding a higher risk of hospital admission for individuals infected with the B.1.1.7 variant compared to wild-type SARS-CoV-2. This increased risk of severity may be specific to adults older than 30 years.

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Markus Hoffmann et al.

Summary: The emergence of the B.1.617 variant in India may be responsible for the sharp increase in COVID-19 cases and deaths. B.1.617 shows increased efficiency in entering cells and evades antibody responses, contributing to its rapid spread.

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Michael Barton et al.

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