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Earlier In Vitro Viral Production With SARS-CoV-2 Alpha Than With Beta, Gamma, B, or A.27 Variants

Since its emergence in China at the end of 2019, SARS-CoV-2 has rapidly spread across the world to become a global public health emergency. Since then, the pandemic has evolved with the large worldwide emergence of new variants, such as the Alpha (B.1.1.7 variant), Beta (B.1.351 variant), and Gamma...

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Autores principales: Lebourgeois, Samuel, Chenane, Houssem Redha, Houhou-Fidouh, Nadhira, Menidjel, Reyene, Ferré, Valentine Marie, Collin, Gilles, Benmalek, Nabil, Coppée, Romain, Larrouy, Lucile, Yazdanpanah, Yazdan, Timsit, Jean-François, Charpentier, Charlotte, Descamps, Diane, Visseaux, Benoit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8716835/
https://www.ncbi.nlm.nih.gov/pubmed/34976868
http://dx.doi.org/10.3389/fcimb.2021.792202
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author Lebourgeois, Samuel
Chenane, Houssem Redha
Houhou-Fidouh, Nadhira
Menidjel, Reyene
Ferré, Valentine Marie
Collin, Gilles
Benmalek, Nabil
Coppée, Romain
Larrouy, Lucile
Yazdanpanah, Yazdan
Timsit, Jean-François
Charpentier, Charlotte
Descamps, Diane
Visseaux, Benoit
author_facet Lebourgeois, Samuel
Chenane, Houssem Redha
Houhou-Fidouh, Nadhira
Menidjel, Reyene
Ferré, Valentine Marie
Collin, Gilles
Benmalek, Nabil
Coppée, Romain
Larrouy, Lucile
Yazdanpanah, Yazdan
Timsit, Jean-François
Charpentier, Charlotte
Descamps, Diane
Visseaux, Benoit
author_sort Lebourgeois, Samuel
collection PubMed
description Since its emergence in China at the end of 2019, SARS-CoV-2 has rapidly spread across the world to become a global public health emergency. Since then, the pandemic has evolved with the large worldwide emergence of new variants, such as the Alpha (B.1.1.7 variant), Beta (B.1.351 variant), and Gamma (P.1 variant), and some other under investigation such as the A.27 in France. Many studies are focusing on antibody neutralisation changes according to the spike mutations, but to date, little is known regarding their respective replication capacities. In this work, we demonstrate that the Alpha variant provides an earlier replication in vitro, on Vero E6 and A549 cells, than Beta, Gamma, A.27, and historical lineages. This earlier replication was associated with higher infectious titres in cell-culture supernatants, in line with the higher viral loads observed among Alpha-infected patients. Interestingly, Beta and Gamma variants presented similar kinetic and viral load than the other non-Alpha-tested variants.
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spelling pubmed-87168352021-12-31 Earlier In Vitro Viral Production With SARS-CoV-2 Alpha Than With Beta, Gamma, B, or A.27 Variants Lebourgeois, Samuel Chenane, Houssem Redha Houhou-Fidouh, Nadhira Menidjel, Reyene Ferré, Valentine Marie Collin, Gilles Benmalek, Nabil Coppée, Romain Larrouy, Lucile Yazdanpanah, Yazdan Timsit, Jean-François Charpentier, Charlotte Descamps, Diane Visseaux, Benoit Front Cell Infect Microbiol Cellular and Infection Microbiology Since its emergence in China at the end of 2019, SARS-CoV-2 has rapidly spread across the world to become a global public health emergency. Since then, the pandemic has evolved with the large worldwide emergence of new variants, such as the Alpha (B.1.1.7 variant), Beta (B.1.351 variant), and Gamma (P.1 variant), and some other under investigation such as the A.27 in France. Many studies are focusing on antibody neutralisation changes according to the spike mutations, but to date, little is known regarding their respective replication capacities. In this work, we demonstrate that the Alpha variant provides an earlier replication in vitro, on Vero E6 and A549 cells, than Beta, Gamma, A.27, and historical lineages. This earlier replication was associated with higher infectious titres in cell-culture supernatants, in line with the higher viral loads observed among Alpha-infected patients. Interestingly, Beta and Gamma variants presented similar kinetic and viral load than the other non-Alpha-tested variants. Frontiers Media S.A. 2021-12-16 /pmc/articles/PMC8716835/ /pubmed/34976868 http://dx.doi.org/10.3389/fcimb.2021.792202 Text en Copyright © 2021 Lebourgeois, Chenane, Houhou-Fidouh, Menidjel, Ferré, Collin, Benmalek, Coppée, Larrouy, Yazdanpanah, Timsit, Charpentier, Descamps and Visseaux https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Lebourgeois, Samuel
Chenane, Houssem Redha
Houhou-Fidouh, Nadhira
Menidjel, Reyene
Ferré, Valentine Marie
Collin, Gilles
Benmalek, Nabil
Coppée, Romain
Larrouy, Lucile
Yazdanpanah, Yazdan
Timsit, Jean-François
Charpentier, Charlotte
Descamps, Diane
Visseaux, Benoit
Earlier In Vitro Viral Production With SARS-CoV-2 Alpha Than With Beta, Gamma, B, or A.27 Variants
title Earlier In Vitro Viral Production With SARS-CoV-2 Alpha Than With Beta, Gamma, B, or A.27 Variants
title_full Earlier In Vitro Viral Production With SARS-CoV-2 Alpha Than With Beta, Gamma, B, or A.27 Variants
title_fullStr Earlier In Vitro Viral Production With SARS-CoV-2 Alpha Than With Beta, Gamma, B, or A.27 Variants
title_full_unstemmed Earlier In Vitro Viral Production With SARS-CoV-2 Alpha Than With Beta, Gamma, B, or A.27 Variants
title_short Earlier In Vitro Viral Production With SARS-CoV-2 Alpha Than With Beta, Gamma, B, or A.27 Variants
title_sort earlier in vitro viral production with sars-cov-2 alpha than with beta, gamma, b, or a.27 variants
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8716835/
https://www.ncbi.nlm.nih.gov/pubmed/34976868
http://dx.doi.org/10.3389/fcimb.2021.792202
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