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- W3188821308 abstract "Defective interfering particles arise spontaneously during a viral infection as mutants lacking essential parts of the viral genome. Their ability to replicate in the presence of the wild-type (WT) virus (at the expense of viable viral particles) is mimicked and exploited by therapeutic interfering particles. We propose a strategy for the design of therapeutic interfering RNAs (tiRNAs) against positive-sense single-stranded RNA viruses that assemble via packaging signal-mediated assembly. These tiRNAs contain both an optimised version of the virus assembly manual that is encoded by multiple dispersed RNA packaging signals and a replication signal for viral polymerase, but lack any protein coding information. We use an intracellular model for hepatitis C viral (HCV) infection that captures key aspects of the competition dynamics between tiRNAs and viral genomes for virally produced capsid protein and polymerase. We show that only a small increase in the assembly and replication efficiency of the tiRNAs compared with WT virus is required in order to achieve a treatment efficacy greater than 99%. This demonstrates that the proposed tiRNA design could be a promising treatment option for RNA viral infections." @default.
- W3188821308 created "2021-08-16" @default.
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- W3188821308 date "2021-12-13" @default.
- W3188821308 modified "2023-10-14" @default.
- W3188821308 title "Therapeutic interfering particles exploiting viral replication and assembly mechanisms show promising performance: a modelling study" @default.
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- W3188821308 doi "https://doi.org/10.1038/s41598-021-03168-0" @default.
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