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Adenovirus 5 Vectors Expressing SARS-CoV-2 Proteins

SARS-CoV-2 coronavirus is a recently identified novel coronavirus that is the causative agent of the COVID-19 pandemic that began in 2020. An intense research effort has been undertaken by the research community in order to better understand the molecular etiology of this virus and its mechanisms of...

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Autores principales: Bachus, Scott, Akkerman, Nikolas, Fulham, Lauren, Graves, Drayson, Stephanson, Caelan, Memon, Harram, Miller, Matthew S., Pelka, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9044955/
https://www.ncbi.nlm.nih.gov/pubmed/35224978
http://dx.doi.org/10.1128/msphere.00998-21
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author Bachus, Scott
Akkerman, Nikolas
Fulham, Lauren
Graves, Drayson
Stephanson, Caelan
Memon, Harram
Miller, Matthew S.
Pelka, Peter
author_facet Bachus, Scott
Akkerman, Nikolas
Fulham, Lauren
Graves, Drayson
Stephanson, Caelan
Memon, Harram
Miller, Matthew S.
Pelka, Peter
author_sort Bachus, Scott
collection PubMed
description SARS-CoV-2 coronavirus is a recently identified novel coronavirus that is the causative agent of the COVID-19 pandemic that began in 2020. An intense research effort has been undertaken by the research community in order to better understand the molecular etiology of this virus and its mechanisms of host cell subjugation and immune system evasion. To facilitate further research into the SARS-CoV-2 coronavirus we have generated adenovirus 5-based viral vectors that express SARS-CoV-2 proteins—S, N, E, NSP7, NSP8, and NSP12 as hemagglutinin (HA)-tagged and untagged variants. We have also engineered two additional viruses that express the S protein receptor binding domain and a fusion of the receptor binding domain to the N protein. We show that these vectors are expressed in several different cell lines by Western blotting and real-time quantitative reverse transcriptase (qRT-PCR), we evaluate the subcellular localization of these viral proteins, and we show that these coronavirus proteins bind to a variety of cellular targets. The flexibility of adenovirus vectors allows them to be used in a variety of cell models and, importantly, in animal models as well. IMPORTANCE The COVID-19 pandemic caused by the SARS-CoV-2 coronavirus has brought untold personal and economic suffering to the world. Intense research has made tremendous progress in understanding how this virus works, yet much research remains to be done as new variants and continued evolution of the virus keep shifting the rules of engagement on the pandemic battlefield. Therefore, wide availability of resources and reagents to study SARS-CoV-2 is essential in overcoming the pandemic and for the prevention of future outbreaks. Our viral vectors provide additional tools for researchers to use in order to better understand the molecular biology of virus-host interactions and other aspects of SARS-CoV-2.
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spelling pubmed-90449552022-04-28 Adenovirus 5 Vectors Expressing SARS-CoV-2 Proteins Bachus, Scott Akkerman, Nikolas Fulham, Lauren Graves, Drayson Stephanson, Caelan Memon, Harram Miller, Matthew S. Pelka, Peter mSphere Resource Report SARS-CoV-2 coronavirus is a recently identified novel coronavirus that is the causative agent of the COVID-19 pandemic that began in 2020. An intense research effort has been undertaken by the research community in order to better understand the molecular etiology of this virus and its mechanisms of host cell subjugation and immune system evasion. To facilitate further research into the SARS-CoV-2 coronavirus we have generated adenovirus 5-based viral vectors that express SARS-CoV-2 proteins—S, N, E, NSP7, NSP8, and NSP12 as hemagglutinin (HA)-tagged and untagged variants. We have also engineered two additional viruses that express the S protein receptor binding domain and a fusion of the receptor binding domain to the N protein. We show that these vectors are expressed in several different cell lines by Western blotting and real-time quantitative reverse transcriptase (qRT-PCR), we evaluate the subcellular localization of these viral proteins, and we show that these coronavirus proteins bind to a variety of cellular targets. The flexibility of adenovirus vectors allows them to be used in a variety of cell models and, importantly, in animal models as well. IMPORTANCE The COVID-19 pandemic caused by the SARS-CoV-2 coronavirus has brought untold personal and economic suffering to the world. Intense research has made tremendous progress in understanding how this virus works, yet much research remains to be done as new variants and continued evolution of the virus keep shifting the rules of engagement on the pandemic battlefield. Therefore, wide availability of resources and reagents to study SARS-CoV-2 is essential in overcoming the pandemic and for the prevention of future outbreaks. Our viral vectors provide additional tools for researchers to use in order to better understand the molecular biology of virus-host interactions and other aspects of SARS-CoV-2. American Society for Microbiology 2022-02-28 /pmc/articles/PMC9044955/ /pubmed/35224978 http://dx.doi.org/10.1128/msphere.00998-21 Text en © Crown copyright 2022. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Resource Report
Bachus, Scott
Akkerman, Nikolas
Fulham, Lauren
Graves, Drayson
Stephanson, Caelan
Memon, Harram
Miller, Matthew S.
Pelka, Peter
Adenovirus 5 Vectors Expressing SARS-CoV-2 Proteins
title Adenovirus 5 Vectors Expressing SARS-CoV-2 Proteins
title_full Adenovirus 5 Vectors Expressing SARS-CoV-2 Proteins
title_fullStr Adenovirus 5 Vectors Expressing SARS-CoV-2 Proteins
title_full_unstemmed Adenovirus 5 Vectors Expressing SARS-CoV-2 Proteins
title_short Adenovirus 5 Vectors Expressing SARS-CoV-2 Proteins
title_sort adenovirus 5 vectors expressing sars-cov-2 proteins
topic Resource Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9044955/
https://www.ncbi.nlm.nih.gov/pubmed/35224978
http://dx.doi.org/10.1128/msphere.00998-21
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