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Reverse Genetics of Avian Coronavirus Infectious Bronchitis Virus

We have developed a reverse genetics system for the avian coronavirus infectious bronchitis virus (IBV) in which a full-length cDNA corresponding to the IBV genome is inserted into the vaccinia virus genome under the control of a T7 promoter sequence. Vaccinia virus as a vector for the full-length I...

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Autores principales: Keep, Sarah M., Bickerton, Erica, Britton, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7121808/
http://dx.doi.org/10.1007/978-1-4939-3414-0_6
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author Keep, Sarah M.
Bickerton, Erica
Britton, Paul
author_facet Keep, Sarah M.
Bickerton, Erica
Britton, Paul
author_sort Keep, Sarah M.
collection PubMed
description We have developed a reverse genetics system for the avian coronavirus infectious bronchitis virus (IBV) in which a full-length cDNA corresponding to the IBV genome is inserted into the vaccinia virus genome under the control of a T7 promoter sequence. Vaccinia virus as a vector for the full-length IBV cDNA has the advantage that modifications can be introduced into the IBV cDNA using homologous recombination, a method frequently used to insert and delete sequences from the vaccinia virus genome. Here, we describe the use of transient dominant selection as a method for introducing modifications into the IBV cDNA; that has been successfully used for the substitution of specific nucleotides, deletion of genomic regions, and the exchange of complete genes. Infectious recombinant IBVs are generated in situ following the transfection of vaccinia virus DNA, containing the modified IBV cDNA, into cells infected with a recombinant fowlpox virus expressing T7 DNA dependant RNA polymerase.
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spelling pubmed-71218082020-04-06 Reverse Genetics of Avian Coronavirus Infectious Bronchitis Virus Keep, Sarah M. Bickerton, Erica Britton, Paul Animal Coronaviruses Article We have developed a reverse genetics system for the avian coronavirus infectious bronchitis virus (IBV) in which a full-length cDNA corresponding to the IBV genome is inserted into the vaccinia virus genome under the control of a T7 promoter sequence. Vaccinia virus as a vector for the full-length IBV cDNA has the advantage that modifications can be introduced into the IBV cDNA using homologous recombination, a method frequently used to insert and delete sequences from the vaccinia virus genome. Here, we describe the use of transient dominant selection as a method for introducing modifications into the IBV cDNA; that has been successfully used for the substitution of specific nucleotides, deletion of genomic regions, and the exchange of complete genes. Infectious recombinant IBVs are generated in situ following the transfection of vaccinia virus DNA, containing the modified IBV cDNA, into cells infected with a recombinant fowlpox virus expressing T7 DNA dependant RNA polymerase. 2015-09-10 /pmc/articles/PMC7121808/ http://dx.doi.org/10.1007/978-1-4939-3414-0_6 Text en © Springer Science+Business Media New York 2016 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Keep, Sarah M.
Bickerton, Erica
Britton, Paul
Reverse Genetics of Avian Coronavirus Infectious Bronchitis Virus
title Reverse Genetics of Avian Coronavirus Infectious Bronchitis Virus
title_full Reverse Genetics of Avian Coronavirus Infectious Bronchitis Virus
title_fullStr Reverse Genetics of Avian Coronavirus Infectious Bronchitis Virus
title_full_unstemmed Reverse Genetics of Avian Coronavirus Infectious Bronchitis Virus
title_short Reverse Genetics of Avian Coronavirus Infectious Bronchitis Virus
title_sort reverse genetics of avian coronavirus infectious bronchitis virus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7121808/
http://dx.doi.org/10.1007/978-1-4939-3414-0_6
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