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SARS-CoV-2 variants reveal features critical for replication in primary human cells

Since entering the human population, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2; the causative agent of Coronavirus Disease 2019 [COVID-19]) has spread worldwide, causing >100 million infections and >2 million deaths. While large-scale sequencing efforts have identified numero...

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Autores principales: Pohl, Marie O., Busnadiego, Idoia, Kufner, Verena, Glas, Irina, Karakus, Umut, Schmutz, Stefan, Zaheri, Maryam, Abela, Irene, Trkola, Alexandra, Huber, Michael, Stertz, Silke, Hale, Benjamin G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8021179/
https://www.ncbi.nlm.nih.gov/pubmed/33760807
http://dx.doi.org/10.1371/journal.pbio.3001006
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author Pohl, Marie O.
Busnadiego, Idoia
Kufner, Verena
Glas, Irina
Karakus, Umut
Schmutz, Stefan
Zaheri, Maryam
Abela, Irene
Trkola, Alexandra
Huber, Michael
Stertz, Silke
Hale, Benjamin G.
author_facet Pohl, Marie O.
Busnadiego, Idoia
Kufner, Verena
Glas, Irina
Karakus, Umut
Schmutz, Stefan
Zaheri, Maryam
Abela, Irene
Trkola, Alexandra
Huber, Michael
Stertz, Silke
Hale, Benjamin G.
author_sort Pohl, Marie O.
collection PubMed
description Since entering the human population, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2; the causative agent of Coronavirus Disease 2019 [COVID-19]) has spread worldwide, causing >100 million infections and >2 million deaths. While large-scale sequencing efforts have identified numerous genetic variants in SARS-CoV-2 during its circulation, it remains largely unclear whether many of these changes impact adaptation, replication, or transmission of the virus. Here, we characterized 14 different low-passage replication-competent human SARS-CoV-2 isolates representing all major European clades observed during the first pandemic wave in early 2020. By integrating viral sequencing data from patient material, virus stocks, and passaging experiments, together with kinetic virus replication data from nonhuman Vero-CCL81 cells and primary differentiated human bronchial epithelial cells (BEpCs), we observed several SARS-CoV-2 features that associate with distinct phenotypes. Notably, naturally occurring variants in Orf3a (Q57H) and nsp2 (T85I) were associated with poor replication in Vero-CCL81 cells but not in BEpCs, while SARS-CoV-2 isolates expressing the Spike D614G variant generally exhibited enhanced replication abilities in BEpCs. Strikingly, low-passage Vero-derived stock preparation of 3 SARS-CoV-2 isolates selected for substitutions at positions 5/6 of E and were highly attenuated in BEpCs, revealing a key cell-specific function to this region. Rare isolate-specific deletions were also observed in the Spike furin cleavage site during Vero-CCL81 passage, but these were rapidly selected against in BEpCs, underscoring the importance of this site for SARS-CoV-2 replication in primary human cells. Overall, our study uncovers sequence features in SARS-CoV-2 variants that determine cell-specific replication and highlights the need to monitor SARS-CoV-2 stocks carefully when phenotyping newly emerging variants or potential variants of concern.
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spelling pubmed-80211792021-04-14 SARS-CoV-2 variants reveal features critical for replication in primary human cells Pohl, Marie O. Busnadiego, Idoia Kufner, Verena Glas, Irina Karakus, Umut Schmutz, Stefan Zaheri, Maryam Abela, Irene Trkola, Alexandra Huber, Michael Stertz, Silke Hale, Benjamin G. PLoS Biol Research Article Since entering the human population, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2; the causative agent of Coronavirus Disease 2019 [COVID-19]) has spread worldwide, causing >100 million infections and >2 million deaths. While large-scale sequencing efforts have identified numerous genetic variants in SARS-CoV-2 during its circulation, it remains largely unclear whether many of these changes impact adaptation, replication, or transmission of the virus. Here, we characterized 14 different low-passage replication-competent human SARS-CoV-2 isolates representing all major European clades observed during the first pandemic wave in early 2020. By integrating viral sequencing data from patient material, virus stocks, and passaging experiments, together with kinetic virus replication data from nonhuman Vero-CCL81 cells and primary differentiated human bronchial epithelial cells (BEpCs), we observed several SARS-CoV-2 features that associate with distinct phenotypes. Notably, naturally occurring variants in Orf3a (Q57H) and nsp2 (T85I) were associated with poor replication in Vero-CCL81 cells but not in BEpCs, while SARS-CoV-2 isolates expressing the Spike D614G variant generally exhibited enhanced replication abilities in BEpCs. Strikingly, low-passage Vero-derived stock preparation of 3 SARS-CoV-2 isolates selected for substitutions at positions 5/6 of E and were highly attenuated in BEpCs, revealing a key cell-specific function to this region. Rare isolate-specific deletions were also observed in the Spike furin cleavage site during Vero-CCL81 passage, but these were rapidly selected against in BEpCs, underscoring the importance of this site for SARS-CoV-2 replication in primary human cells. Overall, our study uncovers sequence features in SARS-CoV-2 variants that determine cell-specific replication and highlights the need to monitor SARS-CoV-2 stocks carefully when phenotyping newly emerging variants or potential variants of concern. Public Library of Science 2021-03-24 /pmc/articles/PMC8021179/ /pubmed/33760807 http://dx.doi.org/10.1371/journal.pbio.3001006 Text en © 2021 Pohl et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Pohl, Marie O.
Busnadiego, Idoia
Kufner, Verena
Glas, Irina
Karakus, Umut
Schmutz, Stefan
Zaheri, Maryam
Abela, Irene
Trkola, Alexandra
Huber, Michael
Stertz, Silke
Hale, Benjamin G.
SARS-CoV-2 variants reveal features critical for replication in primary human cells
title SARS-CoV-2 variants reveal features critical for replication in primary human cells
title_full SARS-CoV-2 variants reveal features critical for replication in primary human cells
title_fullStr SARS-CoV-2 variants reveal features critical for replication in primary human cells
title_full_unstemmed SARS-CoV-2 variants reveal features critical for replication in primary human cells
title_short SARS-CoV-2 variants reveal features critical for replication in primary human cells
title_sort sars-cov-2 variants reveal features critical for replication in primary human cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8021179/
https://www.ncbi.nlm.nih.gov/pubmed/33760807
http://dx.doi.org/10.1371/journal.pbio.3001006
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