Abstract
RNA interference through non-coding microRNAs (miRNAs) represents a vital component of the innate antiviral immune response in plants and invertebrate animals; however, a role for cellular miRNAs in the defence against viral infection in mammalian organisms has thus far remained elusive. Here we show that interferon beta (IFNbeta) rapidly modulates the expression of numerous cellular miRNAs, and that eight of these IFNbeta-induced miRNAs have sequence-predicted targets within the hepatitis C virus (HCV) genomic RNA. The introduction of synthetic miRNA-mimics corresponding to these IFNbeta-induced miRNAs reproduces the antiviral effects of IFNbeta on HCV replication and infection, whereas neutralization of these antiviral miRNAs with anti-miRNAs reduces the antiviral effects of IFNbeta against HCV. In addition, we demonstrate that IFNbeta treatment leads to a significant reduction in the expression of the liver-specific miR-122, an miRNA that has been previously shown to be essential for HCV replication. Therefore, our findings strongly support the notion that mammalian organisms too, through the interferon system, use cellular miRNAs to combat viral infections.
MeSH Terms
Animals
Base Sequence
Cell Line, Tumor
Cells, Cultured
Genome, Viral/genetics
Hepacivirus/genetics,immunology,physiology
Hepatocytes/virology
Humans
Immunity, Innate
Interferon-beta/immunology,metabolism
Mice
Mice, Inbred BALB C
MicroRNAs/genetics,metabolism
RNA Interference
RNA, Viral/genetics,metabolism
Virus Replication
Chemicals
MicroRNAs
RNA, Viral
Interferon-beta
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Pedersen Irene M
Department of Molecular Biology, University of California San Diego, La Jolla, California 92093, USA.
Cheng Guofeng
Wieland Stefan
Volinia Stefano
Croce Carlo M
Chisari Francis V
David Michael
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