Cargando…
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...
Autores principales: | , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1784624402393989120 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8716835 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT lebourgeoissamuel earlierinvitroviralproductionwithsarscov2alphathanwithbetagammabora27variants AT chenanehoussemredha earlierinvitroviralproductionwithsarscov2alphathanwithbetagammabora27variants AT houhoufidouhnadhira earlierinvitroviralproductionwithsarscov2alphathanwithbetagammabora27variants AT menidjelreyene earlierinvitroviralproductionwithsarscov2alphathanwithbetagammabora27variants AT ferrevalentinemarie earlierinvitroviralproductionwithsarscov2alphathanwithbetagammabora27variants AT collingilles earlierinvitroviralproductionwithsarscov2alphathanwithbetagammabora27variants AT benmaleknabil earlierinvitroviralproductionwithsarscov2alphathanwithbetagammabora27variants AT coppeeromain earlierinvitroviralproductionwithsarscov2alphathanwithbetagammabora27variants AT larrouylucile earlierinvitroviralproductionwithsarscov2alphathanwithbetagammabora27variants AT yazdanpanahyazdan earlierinvitroviralproductionwithsarscov2alphathanwithbetagammabora27variants AT timsitjeanfrancois earlierinvitroviralproductionwithsarscov2alphathanwithbetagammabora27variants AT charpentiercharlotte earlierinvitroviralproductionwithsarscov2alphathanwithbetagammabora27variants AT descampsdiane earlierinvitroviralproductionwithsarscov2alphathanwithbetagammabora27variants AT visseauxbenoit earlierinvitroviralproductionwithsarscov2alphathanwithbetagammabora27variants |