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Demonstration of bacterium‐free very rapid reverse genetics system using mumps virus

The reverse genetics system is a very powerful tool for analyzing the molecular mechanisms of viral propagation and pathogenesis. However, full‐length genome plasmid construction is highly time‐consuming and laborious, and undesired mutations may be introduced by Escherichia coli. This study shows a...

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Detalles Bibliográficos
Autores principales: Bae, Chaewon, Katoh, Hiroshi, Wakata, Aika, Sakata, Masafumi, Kato, Fumihiro, Takeda, Makoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092663/
https://www.ncbi.nlm.nih.gov/pubmed/36259144
http://dx.doi.org/10.1111/1348-0421.13032
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author Bae, Chaewon
Katoh, Hiroshi
Wakata, Aika
Sakata, Masafumi
Kato, Fumihiro
Takeda, Makoto
author_facet Bae, Chaewon
Katoh, Hiroshi
Wakata, Aika
Sakata, Masafumi
Kato, Fumihiro
Takeda, Makoto
author_sort Bae, Chaewon
collection PubMed
description The reverse genetics system is a very powerful tool for analyzing the molecular mechanisms of viral propagation and pathogenesis. However, full‐length genome plasmid construction is highly time‐consuming and laborious, and undesired mutations may be introduced by Escherichia coli. This study shows a very rapid E. coli‐free method of full‐genome construction using the mumps virus as an example. This method was able to reduce dramatically the time for full‐genome construction, which was used very efficiently for virus rescue, from several days or more to ~2 days, with a similar accuracy and yield to the conventional method using E. coli/plasmid.
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spelling pubmed-100926632023-04-13 Demonstration of bacterium‐free very rapid reverse genetics system using mumps virus Bae, Chaewon Katoh, Hiroshi Wakata, Aika Sakata, Masafumi Kato, Fumihiro Takeda, Makoto Microbiol Immunol Note The reverse genetics system is a very powerful tool for analyzing the molecular mechanisms of viral propagation and pathogenesis. However, full‐length genome plasmid construction is highly time‐consuming and laborious, and undesired mutations may be introduced by Escherichia coli. This study shows a very rapid E. coli‐free method of full‐genome construction using the mumps virus as an example. This method was able to reduce dramatically the time for full‐genome construction, which was used very efficiently for virus rescue, from several days or more to ~2 days, with a similar accuracy and yield to the conventional method using E. coli/plasmid. John Wiley and Sons Inc. 2022-11-02 2023-01 /pmc/articles/PMC10092663/ /pubmed/36259144 http://dx.doi.org/10.1111/1348-0421.13032 Text en © 2022 The Authors. Microbiology and Immunology published by The Societies and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Note
Bae, Chaewon
Katoh, Hiroshi
Wakata, Aika
Sakata, Masafumi
Kato, Fumihiro
Takeda, Makoto
Demonstration of bacterium‐free very rapid reverse genetics system using mumps virus
title Demonstration of bacterium‐free very rapid reverse genetics system using mumps virus
title_full Demonstration of bacterium‐free very rapid reverse genetics system using mumps virus
title_fullStr Demonstration of bacterium‐free very rapid reverse genetics system using mumps virus
title_full_unstemmed Demonstration of bacterium‐free very rapid reverse genetics system using mumps virus
title_short Demonstration of bacterium‐free very rapid reverse genetics system using mumps virus
title_sort demonstration of bacterium‐free very rapid reverse genetics system using mumps virus
topic Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092663/
https://www.ncbi.nlm.nih.gov/pubmed/36259144
http://dx.doi.org/10.1111/1348-0421.13032
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