Tehran University of Medical Sciences

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Inhibition of Respiratory Syncytial Virus Replication by Simultaneous Targeting of Mrna and Genomic Rna Using Dual-Targeting Sirnas Publisher Pubmed



Malekshahi SS1 ; Salimi V1 ; Arefian E2 ; Fateminasab G1 ; Adjaminejadfard S1 ; Yavarian J1 ; Mokhtariazad T1
Authors
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Authors Affiliations
  1. 1. Virology Department, School of Public Health, Tehran University of Medical Science, Porsina Ave, Tehran, Iran
  2. 2. Department of Microbiology, School of Biology, College of Science, University of Tehran, Tehran, Iran

Source: Molecular Biotechnology Published:2016


Abstract

We attempted to generate siRNAs with two active strands, which can simultaneously knock down the expression of mRNA and viral genomic RNA. In this study, short hairpin RNAs (shRNAs) against N and F genes were used. Expression of F and N mRNA transcripts as well as genomic RNA was determined with relative real-time RT-PCR. The RSV load in infected cell culture supernatant was determined by absolute quantitative real-time PCR. We found that (i) in the presence of shRNA-N, a greater reduction in viral genomic RNA was found; (ii) the level of expression at MOI 0.01 was reduced more than MOI 0.1; (iii) reduction in N transcript was greater than F; and (iv) finally, in combination pre-treatment with two shRNAs, the reduction was not significant as compared to single shRNA transfection. shRNAs also inhibited the production of RSV progeny as shown by viral load in infected HEp-2 cells. (i) Virus load reduction was greater at MOI 0.01 than 0.1 and (ii) significant load reduction was not seen with combination shRNA pre-treatment. The antiviral potency was also confirmed by plaque assay and western blot analysis. Our results provided further evidence that RNAi could be a powerful treatment option against respiratory viruses. © 2016, Springer Science+Business Media New York.