Artículo

Antiviral efficacy of short-hairpin RNAs and artificial microRNAs targeting footand- mouth disease virus

Currá, Anabella Paola Icon; Cacciabue, Marco Polo Domingo Icon; Gravisaco, María José Icon; Asurmendi, Sebastian Icon; Taboga, Oscar Alberto Icon; Gismondi, Maria Ines Icon

Otros responsables

Fecha

06/2021

Editorial

PeerJ Inc

Revista

PeerJ

Título del libro

Nombre del evento

Fecha del evento

Institución organizadora

ISSN

2167-8359

eISSN

ISBN

Idioma

Inglés

Tipo del evento

Resumen

RNA interference (RNAi) is a well-conserved mechanism in eukaryotic cells that directs post-transcriptional gene silencing through small RNA molecules. RNAi has been proposed as an alternative approach for rapid and specific control of viruses including foot-and-mouth disease virus (FMDV), the causative agent of a devastating animal disease with high economic impact. The aim of this work was to assess the antiviral activity of different small RNA shuttles targeting the FMDV RNA-dependent RNA polymerase coding sequence (3D). Three target sequences were predicted within 3D considering RNA accessibility as a major criterion. The silencing efficacy of shorthairpin RNAs (shRNAs) and artificial microRNAs (amiRNAs) targeting the selected sequences was confirmed in fluorescent reporter assays. Furthermore, BHK-21 cells transiently expressing shRNAs or amiRNAs proved 70 to >95% inhibition of FMDV growth. Interestingly, dual expression of amiRNAs did not improve FMDV silencing. Lastly, stable cell lines constitutively expressing amiRNAs were established and characterized in terms of antiviral activity against FMDV. As expected, viral replication in these cell lines was delayed. These results show that the target RNA-accessibilityguided approach for RNAi design rendered efficient amiRNAs that constrain FMDV replication. The application of amiRNAs to complement FMDV vaccination in specific epidemiological scenarios shall be explored further.

Aprobación

Revisión

Complementado por

Referenciado por

Licencia Creative Commons

Excepto donde se indique lo contrario, la licencia de este ítem se describe como by-nc-sa