| Literature DB >> 28678686 |
Shun Chen1,2,3, Wei Zhang2, Qin Zhou2, Anqi Wang2, Lipei Sun2, Mingshu Wang1,3,2, Renyong Jia1,3,2, Dekang Zhu1,3, Mafeng Liu1,3,2, Kunfeng Sun1,3,2, Qiao Yang1,3,2, Ying Wu1,3,2, Xiaoyue Chen1,3, Anchun Cheng2,3,1.
Abstract
Duck plague virus (DPV) is a virus of the Herpesviridae family that leads to acute disease with a high mortality rate in ducks. Control of the disease contributes to the development of poultry breeding. Type III IFN family (IFN-λs) is a novel member of the IFN family, and goose IFN-λ (goIFN-λ) is a newly identified gene whose antiviral function has only been investigated to a limited extent. Here, the cross-species antiviral activity of goIFN-λ against DPV in duck embryo fibroblasts (DEFs) was studied. We found that pre-treatment with goIFN-λ greatly increased the expression of IFN-λ in both heterologous DEFs and homologous goose embryo fibroblasts (GEFs), while differentially inducing IFNα- and IFN-stimulated genes. Additionally, a positive self-regulatory feedback loop of goIFN-λ was blocked by a mouse anti-goIFN-λ polyclonal antibody, which was confirmed in both homologous GEFs and goose peripheral blood mononuclear cells (PBMCs). The suppression of the BAC-DPV-EGFP by goIFN-λ in DEFs was confirmed by fluorescence microscopy, flow cytometry (FCM) analysis, viral copies and titre detection, which can be rescued by mouse anti-goIFN-λ polyclonal antibody incubation. Finally, reporter gene assays indicated that the cross-species antiviral activity of goIFN-λ against BAC-DPV-EGFP is related to its positive self-regulatory feedback loop and subsequent ISG induction. Our data shed light on the fundamental mechanisms of goIFN-λ antiviral function in vitro and extend the considerable range of therapeutic applications in multiple-poultry disease.Entities:
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Year: 2017 PMID: 28678686 DOI: 10.1099/jgv.0.000788
Source DB: PubMed Journal: J Gen Virol ISSN: 0022-1317 Impact factor: 3.891