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首页> 外文期刊>Fish & Shellfish Immunology >Infectious salmon anemia virus segment 7 ORF1 and segment 8 ORF2 proteins inhibit IRF mediated activation of the Atlantic salmon IFNa1 promoter
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Infectious salmon anemia virus segment 7 ORF1 and segment 8 ORF2 proteins inhibit IRF mediated activation of the Atlantic salmon IFNa1 promoter

机译:传染性鲑鱼贫血病毒7片段ORF1和8片段ORF2抑制IRF介导的大西洋鲑鱼IFNa1启动子的激活

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Infectious salmon anemia virus (ISAV) is an orthomyxovirus, which may cause multisystemic disease and high mortality of Atlantic salmon (Salmo solar L). This suggests that ISAV encodes proteins that antagonize the type I interferon (IFN-I) system, which is of crucial importance in innate antiviral immunity. To find out how ISAV might inhibit IFN-I synthesis, we have here studied whether the two ISAV proteins s7ORF1 and s8ORF2 might interfere with activation of the IFNa1 promoter mediated by overexpression of interferon regulatory factors (IRFs) or by the IFN promoter activation protein IPS-1. The IRF tested were IRF1, IRF3, IRF7A and IRF7B. Promoter activation was measured using a luciferase reporter assay where Atlantic salmon TO cells were co-transfected with the IFNa1 promoter reporter plasmid together with an IRF plasmid and the s7ORF1 or the s8ORF2 construct or a control plasmid. The results showed that s7ORF1 significantly inhibited IRF3 and IRF7B induced IFN promoter activity, while s8ORF2 significantly inhibited IRF1 and IRF3 induced promoter activity. Neither s7ORF1 nor s8ORF2 inhibited IPS-1 mediated promoter activation. Immunoprecipitation data suggest that both s7ORF1 and s8ORF2 can bind to all four IRFs. Taken together, this study thus shows that the ISAV proteins s7ORF1 and s8ORF2 antagonizes IFN-I transcription activation mediated by the IRFs. As such this work provides further insight into the pathogenic properties of ISAV. (C) 2016 Elsevier Ltd. All rights reserved.
机译:传染性鲑鱼贫血病毒(ISAV)是一种正粘病毒,它可能引起多系统疾病,并导致大西洋鲑鱼(Salmo solar L)高死亡率。这表明,ISAV编码拮抗I型干扰素(IFN-I)系统的蛋白质,这在先天抗病毒免疫中至关重要。为了找出ISAV如何抑制IFN-1的合成,我们在这里研究了两种ISAV蛋白s7ORF1和s8ORF2是否会干扰由干扰素调节因子(IRFs)或IFN启动子激活蛋白IPS介导的IFNa1启动子的激活。 -1。被测试的IRF为IRF1,IRF3,IRF7A和IRF7B。使用萤光素酶报告基因测定法测量启动子激活,其中将大西洋鲑鱼TO细胞与IFNa1启动子报告质粒以及IRF质粒和s7ORF1或s8ORF2构建体或对照质粒一起共转染。结果表明,s7ORF1显着抑制IRF3和IRF7B诱导的IFN启动子活性,而s8ORF2显着抑制IRF1和IRF3诱导的启动子活性。 s7ORF1和s8ORF2均未抑制IPS-1介导的启动子激活。免疫沉淀数据表明s7ORF1和s8ORF2均可结合所有四个IRF。综上所述,这项研究因此表明,ISAV蛋白s7ORF1和s8ORF2拮抗IRF介导的IFN-I转录激活。这样,这项工作就可以进一步了解ISAV的致病特性。 (C)2016 Elsevier Ltd.保留所有权利。

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