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Updated: Jun 5, 2026

Co-immunoprecipitation of the Mouse Mx1 Protein with the Influenza A Virus Nucleoprotein
Published on: April 21, 2015
Human MxA protein inhibits the replication of classical swine fever virus
Yicheng Zhao1, Daxin Pang, Tiedong Wang
1Department of Animal Biotechnology, Jilin Provincial Key Laboratory of Animal Embryo Engineering, The Center for Animal Embryo Engineering of Jilin Province, College of Animal Science and Veterinary Medicine, Jilin University, 5333 Xi'an Road, Changchun 130062, Jilin, PR China. zhao008@hotmail.com
Abstract:
Classical swine fever virus (CSFV) has a spherical enveloped particle with a single stranded RNA genome, the virus belonging to a pestivirus of the family Flaviviridae is the causative agent of an acute contagious disease classical swine fever (CSF). The interferon-induced MxA protein has been widely shown to inhibit the life cycle of certain RNA viruses as members of the Bunyaviridae family and others. Interestingly, it has been reported that expression of MxA in infected cells was blocked by CSFV and whether MxA has an inhibitory effect against CSFV remains unknown to date until present. Here, we report that CSFV replicated poorly in cells stably transfected with human MxA. The proliferation of progeny virus in both PK-15 cell lines and swine fetal fibroblasts (PEF) continuously expressing MxA was shown significantly inhibited as measured by virus titration, indirect immune fluorescence assay and real-time PCR.
Insights
Human MxA protein significantly inhibits classical swine fever virus (CSFV) replication. This finding reveals a potential antiviral strategy against CSFV, the cause of classical swine fever (CSF).
Area of Science:
- Virology
- Immunology
- Molecular Biology
Background:
- Classical swine fever virus (CSFV) causes a severe contagious disease in pigs.
- Interferon-induced MxA protein is known to inhibit certain RNA viruses.
- CSFV reportedly blocks MxA expression, leaving its effect on CSFV unknown.
Purpose of the Study:
- To investigate the inhibitory effect of human MxA protein on CSFV replication.
- To determine if MxA can be a potential antiviral target against CSFV.
Main Methods:
- Stable transfection of PK-15 cell lines and swine fetal fibroblasts (PEF) with human MxA.
- Infection of MxA-expressing cells with CSFV.
- Quantification of viral replication using virus titration, indirect immune fluorescence assay, and real-time PCR.
Main Results:
- CSFV replicated poorly in cells stably expressing human MxA.
- Proliferation of progeny CSFV was significantly inhibited in MxA-expressing PK-15 and PEF cells.
- Virus titration, immune fluorescence, and real-time PCR confirmed the inhibitory effect.
Conclusions:
- Human MxA protein possesses significant antiviral activity against CSFV.
- MxA effectively inhibits CSFV replication in swine cells.
- MxA represents a potential therapeutic target for controlling classical swine fever.
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