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A resource of human coronavirus protein-coding sequences in a flexible, multipurpose Gateway Entry clone collection

The COVID-19 pandemic has catalyzed unprecedented scientific data and reagent sharing and collaboration, which enabled understanding the virology of the SARS-CoV-2 virus and vaccine development at record speed. The pandemic, however, has also raised awareness of the danger posed by the family of cor...

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Autores principales: Weller, Benjamin, Lin, Chung-Wen, Pogoutse, Oxana, Sauer, Mayra, Marin-de la Rosa, Nora, Strobel, Alexandra, Young, Veronika, Knapp, Jennifer J, Rayhan, Ashyad, Falter, Claudia, Kim, Dae-Kyum, Roth, Frederick P, Falter-Braun, Pascal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320145/
https://www.ncbi.nlm.nih.gov/pubmed/37267226
http://dx.doi.org/10.1093/g3journal/jkad105
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author Weller, Benjamin
Lin, Chung-Wen
Pogoutse, Oxana
Sauer, Mayra
Marin-de la Rosa, Nora
Strobel, Alexandra
Young, Veronika
Knapp, Jennifer J
Rayhan, Ashyad
Falter, Claudia
Kim, Dae-Kyum
Roth, Frederick P
Falter-Braun, Pascal
author_facet Weller, Benjamin
Lin, Chung-Wen
Pogoutse, Oxana
Sauer, Mayra
Marin-de la Rosa, Nora
Strobel, Alexandra
Young, Veronika
Knapp, Jennifer J
Rayhan, Ashyad
Falter, Claudia
Kim, Dae-Kyum
Roth, Frederick P
Falter-Braun, Pascal
author_sort Weller, Benjamin
collection PubMed
description The COVID-19 pandemic has catalyzed unprecedented scientific data and reagent sharing and collaboration, which enabled understanding the virology of the SARS-CoV-2 virus and vaccine development at record speed. The pandemic, however, has also raised awareness of the danger posed by the family of coronaviruses, of which 7 are known to infect humans and dozens have been identified in reservoir species, such as bats, rodents, or livestock. To facilitate understanding the commonalities and specifics of coronavirus infections and aspects of viral biology that determine their level of lethality to the human host, we have generated a collection of freely available clones encoding nearly all human coronavirus proteins known to date. We hope that this flexible, Gateway-compatible vector collection will encourage further research into the interactions of coronaviruses with their human host, to increase preparedness for future zoonotic viral outbreaks.
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spelling pubmed-103201452023-07-06 A resource of human coronavirus protein-coding sequences in a flexible, multipurpose Gateway Entry clone collection Weller, Benjamin Lin, Chung-Wen Pogoutse, Oxana Sauer, Mayra Marin-de la Rosa, Nora Strobel, Alexandra Young, Veronika Knapp, Jennifer J Rayhan, Ashyad Falter, Claudia Kim, Dae-Kyum Roth, Frederick P Falter-Braun, Pascal G3 (Bethesda) Investigation The COVID-19 pandemic has catalyzed unprecedented scientific data and reagent sharing and collaboration, which enabled understanding the virology of the SARS-CoV-2 virus and vaccine development at record speed. The pandemic, however, has also raised awareness of the danger posed by the family of coronaviruses, of which 7 are known to infect humans and dozens have been identified in reservoir species, such as bats, rodents, or livestock. To facilitate understanding the commonalities and specifics of coronavirus infections and aspects of viral biology that determine their level of lethality to the human host, we have generated a collection of freely available clones encoding nearly all human coronavirus proteins known to date. We hope that this flexible, Gateway-compatible vector collection will encourage further research into the interactions of coronaviruses with their human host, to increase preparedness for future zoonotic viral outbreaks. Oxford University Press 2023-06-02 /pmc/articles/PMC10320145/ /pubmed/37267226 http://dx.doi.org/10.1093/g3journal/jkad105 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of The Genetics Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigation
Weller, Benjamin
Lin, Chung-Wen
Pogoutse, Oxana
Sauer, Mayra
Marin-de la Rosa, Nora
Strobel, Alexandra
Young, Veronika
Knapp, Jennifer J
Rayhan, Ashyad
Falter, Claudia
Kim, Dae-Kyum
Roth, Frederick P
Falter-Braun, Pascal
A resource of human coronavirus protein-coding sequences in a flexible, multipurpose Gateway Entry clone collection
title A resource of human coronavirus protein-coding sequences in a flexible, multipurpose Gateway Entry clone collection
title_full A resource of human coronavirus protein-coding sequences in a flexible, multipurpose Gateway Entry clone collection
title_fullStr A resource of human coronavirus protein-coding sequences in a flexible, multipurpose Gateway Entry clone collection
title_full_unstemmed A resource of human coronavirus protein-coding sequences in a flexible, multipurpose Gateway Entry clone collection
title_short A resource of human coronavirus protein-coding sequences in a flexible, multipurpose Gateway Entry clone collection
title_sort resource of human coronavirus protein-coding sequences in a flexible, multipurpose gateway entry clone collection
topic Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320145/
https://www.ncbi.nlm.nih.gov/pubmed/37267226
http://dx.doi.org/10.1093/g3journal/jkad105
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