Abstract
The role of microRNA (miRNA) in influenza A virus (IAV) host species specificity is not well understood as yet. Here, we show that a host miRNA, miR-1290, is induced through the extracellular signal-regulated kinase (ERK) pathway upon IAV infection and is associated with increased viral titers in human cells and ferret animal models. miR-1290 was observed to target and reduce expression of the host vimentin gene. Vimentin binds with the PB2 subunit of influenza A virus ribonucleoprotein (vRNP), and knockdown of vimentin expression significantly increased vRNP nuclear retention and viral polymerase activity. Interestingly, miR-1290 was not detected in either chicken cells or mouse animal models, and the 3′ UTR of the chicken vimentin gene contains no binding site for miR-1290. These findings point to a host species-specific mechanism by which IAV upregulates miR-1290 to disrupt vimentin expression and retain vRNP in the nucleus, thereby enhancing viral polymerase activity and viral replication.
Original language | English |
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Pages (from-to) | 10-23 |
Number of pages | 14 |
Journal | Molecular Therapy - Nucleic Acids |
Volume | 17 |
DOIs | |
State | Published - 06 09 2019 |
Bibliographical note
Publisher Copyright:© 2019
Keywords
- ferret
- host species-specificity
- influenza A virus
- miR-1290
- miRNA
- vRNP
- vimentin
- viral ribonucleoprotein
- virus