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Novel Role for miR-1290 in Host Species Specificity of Influenza A Virus

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 hu...

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Detalles Bibliográficos
Autores principales: Huang, Sheng-Yu, Huang, Chih-Heng, Chen, Chi-Jene, Chen, Ting-Wen, Lin, Chun-Yuan, Lin, Yueh-Te, Kuo, Shu-Ming, Huang, Chung-Guei, Lee, Li-Ang, Chen, Yi-Hsiang, Chen, Mei-Feng, Kuo, Rei-Lin, Shih, Shin-Ru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6554369/
https://www.ncbi.nlm.nih.gov/pubmed/31173947
http://dx.doi.org/10.1016/j.omtn.2019.04.028
Descripción
Sumario: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.