1. Porcine IFITM1 is a host restriction factor that inhibits pseudorabies virus infection
- Author
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Sheng-Li Ming, Bei-Bei Chu, Bing-Qian Su, Jiang Wang, Guo-Yu Yang, Meng-Di Wang, Chun-Feng Wang, Lei Zeng, Guo-Li Li, and Qi Wang
- Subjects
Swine ,animal diseases ,viruses ,Pseudorabies ,02 engineering and technology ,Dengue virus ,medicine.disease_cause ,Virus Replication ,Biochemistry ,Antiviral Agents ,Virus ,Cell Line ,03 medical and health sciences ,Structural Biology ,Viral entry ,Influenza A virus ,medicine ,Animals ,Humans ,Amino Acid Sequence ,Molecular Biology ,030304 developmental biology ,0303 health sciences ,biology ,virus diseases ,DNA virus ,General Medicine ,biochemical phenomena, metabolism, and nutrition ,Virus Internalization ,021001 nanoscience & nanotechnology ,biology.organism_classification ,Virology ,Antigens, Differentiation ,Herpesvirus 1, Suid ,Immunity, Innate ,Type I interferon signaling pathway ,Gene Expression Regulation ,Gene Knockdown Techniques ,Host-Pathogen Interactions ,0210 nano-technology ,IRF3 - Abstract
Interferon-inducible transmembrane proteins (IFITMs) restrict infection by several viruses, such as influenza A virus, West Nile virus and dengue virus. It has not been determined whether porcine IFITMs (pIFITMs) inhibit infection by pseudorabies virus (PRV), an enveloped, double-stranded DNA virus, which is the etiological agent of Aujeszky's disease in pigs. Here, we report that PRV infection elicited pIFITM1 expression in PK15 porcine kidney epithelial cells and 3D4/21 alveolar macrophages. pIFITM2 and pIFITM3 expression was only elevated in PK15 cells during PRV infection. Depletion of pIFITM1 using RNA interference, either in PK15 or in 3D4/21 cells, enhanced PRV infection while overexpression of pIFITM1 had the opposite effect. Knockdown of pIFITM2 and pIFITM3 did not influence PRV infection, suggesting that pIFITM2 and pIFITM3 are independent of PRV infection. PRV-induced pIFITM1 expression was dependent on the cGAS/STING/TBK1/IRF3 innate immune pathway and interferon-alpha receptor-1, suggesting that pIFITM1 is up-regulated by the type I interferon signaling pathway. The anti-PRV role of pIFITM1 was inhibited upon PRV entry. Our data demonstrate that pIFITM1 is a host restriction factor that inhibits PRV entry that may shed light on a strategy for prevention of PRV infection.
- Published
- 2019