Porcine Reproductive and Respiratory Syndrome Virus Nsp1β Inhibits Interferon-Activated JAK/STAT Signal Transduction by Inducing Karyopherin-α1 Degradation

被引:107
作者
Wang, Rong
Nan, Yuchen
Yu, Ying
Zhang, Yan-Jin [1 ]
机构
[1] Univ Maryland, VA MD Reg Coll Vet Med, Mol Virol Lab, College Pk, MD 20742 USA
关键词
NONSTRUCTURAL PROTEIN 1-BETA; NUCLEAR IMPORT; MORPHOLINO OLIGOMERS; GNOTOBIOTIC PIGS; LELYSTAD-VIRUS; I INTERFERONS; REPLICATION; STAT1; CELLS; IDENTIFICATION;
D O I
10.1128/JVI.02643-12
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Porcine reproductive and respiratory syndrome virus (PRRSV) inhibits the interferon-mediated antiviral response. Type I interferons (IFNs) induce the expression of IFN-stimulated genes by activating phosphorylation of both signal transducer and activator of transcription 1 (STAT1) and STAT2, which form heterotrimers (interferon-stimulated gene factor 3 [ISGF3]) with interferon regulatory factor 9 (IRF9) and translocate to the nucleus. PRRSV Nsp1 beta blocks the nuclear translocation of the ISGF3 complex by an unknown mechanism. In this study, we discovered that Nsp1 beta induced the degradation of karyopherin-alpha 1 (KPNA1, also called importin-alpha 5), which is known to mediate the nuclear import of ISGF3. Overexpression of Nsp1 beta resulted in a reduction of KPNA1 levels in a dose-dependent manner, and treatment of the cells with the proteasome inhibitor MG132 restored KPNA1 levels. Furthermore, the presence of Nsp1 beta induced an elevation of KPNA1 ubiquitination and a shortening of its half-life. Our analysis of Nsp1 beta deletion constructs showed that the N-terminal domain of Nsp1 beta was involved in the ubiquitin-proteasomal degradation of KPNA1. A nucleotide substitution resulting in an amino acid change from valine to isoleucine at residue 19 of Nsp1 beta diminished its ability to induce KPNA1 degradation and to inhibit IFN-mediated signaling. Interestingly, infection of MARC-145 cells by PRRSV strains VR-2332 and VR-2385 also resulted in KPNA1 reduction, whereas infection by an avirulent strain, Ingelvac PRRS modified live virus (MLV), did not. MLV Nsp1 beta had no effect on KPNA1; however, a mutant with an amino acid change at residue 19 from isoleucine to valine induced KPNA1 degradation. These results indicate that Nsp1 beta blocks ISGF3 nuclear translocation by inducing KPNA1 degradation and that valine-19 in Nsp1 beta correlates with the inhibition.
引用
收藏
页码:5219 / 5228
页数:10
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