一种由 NF-κB 调节的细胞因子可增强家蚕的抗病毒能力

IF 2.3 2区 农林科学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Dongmei Wei, Jinming Liu, Jie Hu, Beilei Zhang, Yumeng Pan, Qingyou Xia, Fei Wang
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引用次数: 0

摘要

昆虫 NF-κB 样因子 Relish 可被病毒感染激活并诱导产生抗病毒蛋白。在这项研究中,我们对表达 BmRelish 活性形式(BmRelishact)的 BmE 细胞进行了转录组分析,发现 BmVago-like 是诱导最强的分泌蛋白。BmVago-like 的表达是由 BmNPV 感染蚕蛾核型多角体病毒(BmNPV)特异性触发的,并由 BmSTING-BmRelish 通路调控。用表达 BmVago-like 的细胞或重组 BmVago-like 蛋白(rBmVago-like)的上清培养基孵育新培养的细胞,可显著提高抗病毒性。相反,通过 RNA 干扰(RNAi)减少 BmE 细胞和家蚕幼虫中 BmVago-like 的表达会削弱抗病毒反应。此外,我们还构建了过度表达BmVago-like(BmVago-likeOV)的转基因蚕品系,发现与野生型对照相比,它们在感染BmNPV后病毒载量明显降低,存活率也更高。共免疫沉淀实验表明,Bmintegrin β1与BmVago-like相互作用,参与了BmVago-like介导的抗病毒反应。最后,我们发现 JAK-STAT 通路信号分子的表达水平在 rBmVago-like 处理的细胞和 BmVago-likeOV 蚕幼虫中增加,但在 RNAi 处理的细胞中降低。总之,我们的研究发现了由细胞因子 BmVago-like 介导的家蚕诱导性抗病毒反应,BmVago-like 是 BmSTING-BmRelish 通路的下游效应因子,具有抗病毒细胞因子的功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An NF-κB-regulated cytokine enhances the antiviral resistance of silkworm, Bombyx mori.

Insect NF-κB-like factor, Relish, is activated by viral infection and induces the production of antiviral proteins. In this study, we performed a transcriptomic analysis of BmE cells expressing the active form of BmRelish (BmRelishact) and identified BmVago-like as the most strongly-induced secreted-protein. Expression of BmVago-like was specifically triggered by Bombyx mori Nucleo Polyhedro Virus (BmNPV) infection and regulated by BmSTING-BmRelish pathway. Incubating the fresh culture of cells with supernatant medium of BmVago-like expressing cells or recombinant BmVago-like protein (rBmVago-like) significantly increased antiviral resistance. On the contrary, reducing the expression of Bmvago-like by RNA interference (RNAi) in BmE cells as well as in silkworm larvae impaired antiviral response. Furthermore, we constructed transgenic silkworm line over-expressing BmVago-like (BmVago-likeOV) and found they had markedly lower viral load and higher survival rate after BmNPV infection compared with the wild-type control. Co-immunoprecipitation assay showed Bmintegrin β1 interacts with BmVago-like and it was involved in BmVago-like mediated antiviral response. Finally, we found the expression level of signalling molecules in the JAK-STAT pathway increased in rBmVago-like-treated cells and BmVago-likeOV silkworm larvae but decreased in RNAi-treated cells. In summary, our research uncovered an inducible antiviral response in silkworm mediated by cytokine BmVago-like, which is the downstream effector of BmSTING-BmRelish pathway and functions as an antiviral cytokine.

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来源期刊
Insect Molecular Biology
Insect Molecular Biology 生物-昆虫学
CiteScore
4.80
自引率
3.80%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Insect Molecular Biology has been dedicated to providing researchers with the opportunity to publish high quality original research on topics broadly related to insect molecular biology since 1992. IMB is particularly interested in publishing research in insect genomics/genes and proteomics/proteins. This includes research related to: • insect gene structure • control of gene expression • localisation and function/activity of proteins • interactions of proteins and ligands/substrates • effect of mutations on gene/protein function • evolution of insect genes/genomes, especially where principles relevant to insects in general are established • molecular population genetics where data are used to identify genes (or regions of genomes) involved in specific adaptations • gene mapping using molecular tools • molecular interactions of insects with microorganisms including Wolbachia, symbionts and viruses or other pathogens transmitted by insects Papers can include large data sets e.g.from micro-array or proteomic experiments or analyses of genome sequences done in silico (subject to the data being placed in the context of hypothesis testing).
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