tetano
Editor, Senior Moderator
PLoS One
. 2024 Nov 8;19(11):e0312776.
doi: 10.1371/journal.pone.0312776. eCollection 2024. In vitro one-pot construction of influenza viral genomes for virus particle synthesis based on reverse genetics system
Ryota Tanaka[SUP] 1 [/SUP], Kenji Tamao[SUP] 1 [/SUP], Mana Ono[SUP] 1 [/SUP], Seiya Yamayoshi[SUP] 2 3 [/SUP], Yoshihiro Kawaoka[SUP] 2 3 4 5 [/SUP], Masayuki Su'etsugu[SUP] 6 [/SUP], Hiroyuki Noji[SUP] 1 [/SUP], Kazuhito V Tabata[SUP] 1 [/SUP]
Affiliations
The reverse genetics system, which allows the generation of influenza viruses from plasmids encoding viral genome, is a powerful tool for basic research on viral infection mechanisms and application research such as vaccine development. However, conventional plasmid construction using Escherichia coli (E.coli) cloning is time-consuming and has difficulties handling DNA encoding genes toxic for E.coli or highly repeated sequences. These limitations hamper rapid virus synthesis. In this study, we establish a very rapid in vitro one-pot plasmid construction (IVOC) based virus synthesis. This method dramatically reduced the time for genome plasmid construction, which was used for virus synthesis, from several days or more to about 8 hours. Moreover, infectious viruses could be synthesized with a similar yield to the conventional E.coli cloning-based method with high accuracy. The applicability of this method was also demonstrated by the generation of recombinant viruses carrying reporter genes from the IVOC products. This method enables the pathogenicity analysis and vaccine development using genetically modified viruses, and it is expected to allow for faster analysis of newly emerging variants than ever before. Furthermore, its application to other RNA viruses is also expected.
. 2024 Nov 8;19(11):e0312776.
doi: 10.1371/journal.pone.0312776. eCollection 2024. In vitro one-pot construction of influenza viral genomes for virus particle synthesis based on reverse genetics system
Ryota Tanaka[SUP] 1 [/SUP], Kenji Tamao[SUP] 1 [/SUP], Mana Ono[SUP] 1 [/SUP], Seiya Yamayoshi[SUP] 2 3 [/SUP], Yoshihiro Kawaoka[SUP] 2 3 4 5 [/SUP], Masayuki Su'etsugu[SUP] 6 [/SUP], Hiroyuki Noji[SUP] 1 [/SUP], Kazuhito V Tabata[SUP] 1 [/SUP]
Affiliations
- PMID: 39514509
- PMCID: PMC11548778
- DOI: 10.1371/journal.pone.0312776
The reverse genetics system, which allows the generation of influenza viruses from plasmids encoding viral genome, is a powerful tool for basic research on viral infection mechanisms and application research such as vaccine development. However, conventional plasmid construction using Escherichia coli (E.coli) cloning is time-consuming and has difficulties handling DNA encoding genes toxic for E.coli or highly repeated sequences. These limitations hamper rapid virus synthesis. In this study, we establish a very rapid in vitro one-pot plasmid construction (IVOC) based virus synthesis. This method dramatically reduced the time for genome plasmid construction, which was used for virus synthesis, from several days or more to about 8 hours. Moreover, infectious viruses could be synthesized with a similar yield to the conventional E.coli cloning-based method with high accuracy. The applicability of this method was also demonstrated by the generation of recombinant viruses carrying reporter genes from the IVOC products. This method enables the pathogenicity analysis and vaccine development using genetically modified viruses, and it is expected to allow for faster analysis of newly emerging variants than ever before. Furthermore, its application to other RNA viruses is also expected.