Citation

  • Authors: Li, M., Yan, K., Wei, L., Yang, J., Lu, C., Xiong, F., Zheng, C., Xu, W.
  • Year: 2015
  • Journal: Antiviral Res 123 50-61
  • Applications: in vitro / in vivo / DNA, siRNA / in vivo-jetPEI-Gal, INTERFERin
  • Cell type: HeLa
    Description: Human cervix epitheloid carcinoma cells

Method

Mice were retroorbitally injected with 1.0 ml reagent containing 50 ug of ZAPexpression plasmid or vector plasmid using in vivo-JetPEI–Gal transfection agent according to the manufacturer’s instructions. Mice received 2 doses of ZAP plasmids, 2 days before and 1 day after CVB3 infection to sustain in vivo over-expression of ZAP.

Abstract

The host Zinc finger antiviral protein (ZAP) has been reported exhibiting antiviral activity against positive-stranded RNA viruses (Togaviridae), negative-stranded RNA viruses (Filoviridae) and retroviruses (Retroviridae). However, whether ZAP restricts the infection of enterovirus and the development of enterovirus mediated disease remains unknown. Here, we reported the antiviral properties of ZAP against coxsackievirus B3 (CVB3), a single-stranded RNA virus of the Enterovirus genus within the Picornaviridae as a major causative agent of viral myocarditis (VMC). We found that the expression of ZAP was significantly induced after CVB3 infection in heart tissues of VMC mice. ZAP potently inhibited CVB3 replication in cells after infection, while overexpression of ZAP in mice significantly increased the resistance to CVB3 replication and viral myocarditis by significantly reducing cardiac inflammatory cytokine production. The ZAP-responsive elements (ZREs) were mapped to the 3'UTR and 5'UTR of viral RNA. Taken together, ZAP confers resistance to CVB3 infection via directly targeting viral RNA and protects mice from acute myocarditis by suppressing viral replication and cardiac inflammatory cytokine production. Our finding further expands ZAP's range of viral targets, and suggests ZAP as a potential therapeutic target for viral myocarditis caused by CVB3.

Pubmed