Key result
PCBP1 knockout in pigs significantly reduced Classical swine fever virus (CSFV) infection in primary cells and activated type I interferon antiviral responses.
Why the study?
Classical swine fever virus causes severe economic losses worldwide, and PCBP1 plays a vital role in viral growth.
PCBP1 knockout pigs generated via CRISPR/Cas9 exhibit normal development and significant resistance to Classical swine fever virus (CSFV) infection, providing a novel animal model for antiviral research.
Provides a novel transgenic swine model for viral resistance; leaves open whether targeting this.
Classical swine fever virus (CSFV), pathogen of classic swine fever, has caused severe economic losses worldwide. Poly (rC)-binding protein 1 (PCBP1), interacting with N pro of CSFV, plays a vital role in CSFV growth. Here, our research is the first report to generate PCBP1 knockout pigs via gene editing technology. The PCBP1 knockout pigs exhibited normal birth weight, reproductive-performance traits, and developed normally. Viral challenge results indicated that primary cells isolated from F 0 and F 1 generation pigs could significantly reduce CSFV infection. Additional mechanism exploration further confirmed that PCBP1 KO mediated antiviral effect is related with the activation of type I interferon. Beyond showing that gene editing strategy can be used to generate PCBP1 KO pigs, our study introduces a valuable animal model for further investigating infection mechanisms of CSFV that help to develop better antiviral solution. Importance As a negative regulator in immune modulation, the effects of PCBP1 on viral replication have been found to be valuable. Here, this study was the first report to generate PCBP1 knockout pigs with normal pregnancy rate and viability. Primary cells isolated from F 0 and F 1 generation PCBP1 knockout pigs could significantly reduce CSFV infection. The PCBP1 knockout pigs could be used as a natural host models for investigating the effects of PCBP1-mediating critical interactions on viral replication and helping to develop better antiviral solution.
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Qi et al. (2021) studied Classical swine fever virus (CSFV) infection. PCBP1 knockout vs. Wild type was evaluated on CSFV proliferation in primary cells. PCBP1 knockout in pigs significantly reduced Classical swine fever virus (CSFV) infection in primary cells and activated type I interferon antiviral responses.
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