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SARS‐CoV‐2 B.1.617 Indian variants: Are electrostatic potential changes responsible for a higher transmission rate?
Lineage B.1.617+, also known as G/452R.V3 and now denoted by WHO with the Greek letters δ and κ, is a recently described SARS‐CoV‐2 variant under investigation first identified in October 2020 in India. As of May 2021, three sublineages labeled as B.1.617.1 (κ), B.1.617.2 (δ), and B.1.617.3 have bee...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8426736/ https://www.ncbi.nlm.nih.gov/pubmed/34260088 http://dx.doi.org/10.1002/jmv.27210 |
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author | Pascarella, Stefano Ciccozzi, Massimo Zella, Davide Bianchi, Martina Benedetti, Francesca Benvenuto, Domenico Broccolo, Francesco Cauda, Roberto Caruso, Arnaldo Angeletti, Silvia Giovanetti, Marta Cassone, Antonio |
author_facet | Pascarella, Stefano Ciccozzi, Massimo Zella, Davide Bianchi, Martina Benedetti, Francesca Benvenuto, Domenico Broccolo, Francesco Cauda, Roberto Caruso, Arnaldo Angeletti, Silvia Giovanetti, Marta Cassone, Antonio |
author_sort | Pascarella, Stefano |
collection | PubMed |
description | Lineage B.1.617+, also known as G/452R.V3 and now denoted by WHO with the Greek letters δ and κ, is a recently described SARS‐CoV‐2 variant under investigation first identified in October 2020 in India. As of May 2021, three sublineages labeled as B.1.617.1 (κ), B.1.617.2 (δ), and B.1.617.3 have been already identified, and their potential impact on the current pandemic is being studied. This variant has 13 amino acid changes, three in its spike protein, which are currently of particular concern: E484Q, L452R, and P681R. Here, we report a major effect of the mutations characterizing this lineage, represented by a marked alteration of the surface electrostatic potential (EP) of the receptor‐binding domain (RBD) of the spike protein. Enhanced RBD‐EP is particularly noticeable in the B.1.617.2 (δ) sublineage, which shows multiple replacements of neutral or negatively charged amino acids with positively charged amino acids. We here hypothesize that this EP change can favor the interaction between the B.1.617+ RBD and the negatively charged ACE2, thus conferring a potential increase in the virus transmission. |
format | Online Article Text |
id | pubmed-8426736 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84267362021-09-09 SARS‐CoV‐2 B.1.617 Indian variants: Are electrostatic potential changes responsible for a higher transmission rate? Pascarella, Stefano Ciccozzi, Massimo Zella, Davide Bianchi, Martina Benedetti, Francesca Benvenuto, Domenico Broccolo, Francesco Cauda, Roberto Caruso, Arnaldo Angeletti, Silvia Giovanetti, Marta Cassone, Antonio J Med Virol Research Articles Lineage B.1.617+, also known as G/452R.V3 and now denoted by WHO with the Greek letters δ and κ, is a recently described SARS‐CoV‐2 variant under investigation first identified in October 2020 in India. As of May 2021, three sublineages labeled as B.1.617.1 (κ), B.1.617.2 (δ), and B.1.617.3 have been already identified, and their potential impact on the current pandemic is being studied. This variant has 13 amino acid changes, three in its spike protein, which are currently of particular concern: E484Q, L452R, and P681R. Here, we report a major effect of the mutations characterizing this lineage, represented by a marked alteration of the surface electrostatic potential (EP) of the receptor‐binding domain (RBD) of the spike protein. Enhanced RBD‐EP is particularly noticeable in the B.1.617.2 (δ) sublineage, which shows multiple replacements of neutral or negatively charged amino acids with positively charged amino acids. We here hypothesize that this EP change can favor the interaction between the B.1.617+ RBD and the negatively charged ACE2, thus conferring a potential increase in the virus transmission. John Wiley and Sons Inc. 2021-07-27 2021-12 /pmc/articles/PMC8426736/ /pubmed/34260088 http://dx.doi.org/10.1002/jmv.27210 Text en © 2021 The Authors. Journal of Medical Virology Published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Pascarella, Stefano Ciccozzi, Massimo Zella, Davide Bianchi, Martina Benedetti, Francesca Benvenuto, Domenico Broccolo, Francesco Cauda, Roberto Caruso, Arnaldo Angeletti, Silvia Giovanetti, Marta Cassone, Antonio SARS‐CoV‐2 B.1.617 Indian variants: Are electrostatic potential changes responsible for a higher transmission rate? |
title | SARS‐CoV‐2 B.1.617 Indian variants: Are electrostatic potential changes responsible for a higher transmission rate? |
title_full | SARS‐CoV‐2 B.1.617 Indian variants: Are electrostatic potential changes responsible for a higher transmission rate? |
title_fullStr | SARS‐CoV‐2 B.1.617 Indian variants: Are electrostatic potential changes responsible for a higher transmission rate? |
title_full_unstemmed | SARS‐CoV‐2 B.1.617 Indian variants: Are electrostatic potential changes responsible for a higher transmission rate? |
title_short | SARS‐CoV‐2 B.1.617 Indian variants: Are electrostatic potential changes responsible for a higher transmission rate? |
title_sort | sars‐cov‐2 b.1.617 indian variants: are electrostatic potential changes responsible for a higher transmission rate? |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8426736/ https://www.ncbi.nlm.nih.gov/pubmed/34260088 http://dx.doi.org/10.1002/jmv.27210 |
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