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Knockout of IRF7 Highlights its Modulator Function of Host Response Against Avian Influenza Virus and the Involvement of MAPK and TOR Signaling Pathways in Chicken

机译:IRF7的基因敲除突出了其宿主抗禽流感病毒的调节功能以及鸡中MAPK和TOR信号通路的参与

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摘要

Interferon regulatory factor 7 (IRF7) is known as the master transcription factor of the type I interferon response in mammalian species along with IRF3. Yet birds only have IRF7, while they are missing IRF3, with a smaller repertoire of immune-related genes, which leads to a distinctive immune response in chickens compared to in mammals. In order to understand the functional role of IRF7 in the regulation of the antiviral response against avian influenza virus in chickens, we generated chicken embryonic fibroblast (DF-1) cell lines and respective controls ( ) by utilizing the CRISPR/Cas9 (clustered regularly interspaced short palindromic repeats/CRISPR-associated protein 9) system. IRF7 knockout resulted in increased viral titers of low pathogenic avian influenza viruses. Further RNA-sequencing performed on H6N2-infected and cell lines revealed that the deletion of IRF7 resulted in the significant down-regulation of antiviral effectors and the differential expression of genes in the MAPK (mitogen-activated protein kinase) and mTOR (mechanistic target of rapamycin) signaling pathways. Dynamic gene expression profiling of the host response between the wildtype and IRF7 knockout revealed potential signaling pathways involving (activator protein 1), (nuclear factor kappa B) and inflammatory cytokines that may complement chicken IRF7. Our findings in this study provide novel insights that have not been reported previously, and lay a solid foundation for enhancing our understanding of the host antiviral response against the avian influenza virus in chickens.
机译:干扰素调节因子7(IRF7)与IRF3一起是哺乳动物物种中I型干扰素应答的主要转录因子。然而,禽只只有IRF7,而缺少IRF3,其免疫相关基因的组成较小,与哺乳动物相比,它在鸡中产生了独特的免疫反应。为了了解IRF7在调节鸡抗禽流感病毒的抗病毒应答中的功能,我们利用CRISPR / Cas9(有规律地间隔排列)生成了鸡胚成纤维细胞(DF-1)细胞系和相应的对照()。短回文重复/ CRISPR相关蛋白9)系统。 IRF7敲除导致低致病性禽流感病毒的病毒滴度增加。对H6N2感染和细胞株进行的进一步RNA测序表明,IRF7的缺失导致抗病毒效应子的显着下调以及MAPK(促分裂原激活的蛋白激酶)和mTOR(MTOR的机械靶标)中基因的差异表达。雷帕霉素)信号通路。野生型和IRF7敲除之间的宿主反应的动态基因表达谱揭示了潜在的信号传导途径,涉及(激活蛋白1),(核因子κB)和可能与鸡IRF7互补的炎性细胞因子。我们在这项研究中的发现提供了以前未曾报道过的新颖见解,并为增进我们对鸡抗禽流感病毒宿主抗病毒反应的了解奠定了坚实的基础。

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