Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore; Zhejiang University-University of Edinburgh Institute, Zhejiang University School of Medicine, Zhejiang University International Campus, Haining, China; Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore; University of Chinese Academy of Sciences, Beijing, China; Key Laboratory of Special Pathogens, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.
Cell Rep. 2020 Nov 3;33(5):108345. doi: 10.1016/j.celrep.2020.108345.
Bat cells and tissue have elevated basal expression levels of antiviral genes commonly associated with interferon alpha (IFNα) signaling. Here, we show Interferon Regulatory Factor 1 (IRF1), 3, and 7 levels are elevated in most bat tissues and that, basally, IRFs contribute to the expression of type I IFN ligands and high expression of interferon regulated genes (IRGs). CRISPR knockout (KO) of IRF 1/3/7 in cells reveals distinct subsets of genes affected by each IRF in an IFN-ligand signaling-dependent and largely independent manner. As the master regulators of innate immunity, the IRFs control the kinetics and maintenance of the IRG response and play essential roles in response to influenza A virus (IAV), herpes simplex virus 1 (HSV-1), Melaka virus/Pteropine orthoreovirus 3 Melaka (PRV3M), and Middle East respiratory syndrome-related coronavirus (MERS-CoV) infection. With its differential expression in bats compared to that in humans, this highlights a critical role for basal IRF expression in viral responses and potentially immune cell development in bats with relevance for IRF function in human biology.
蝙蝠细胞和组织中抗病毒基因的基础表达水平升高,这些基因通常与干扰素 α(IFNα)信号有关。在这里,我们发现干扰素调节因子 1(IRF1)、3 和 7 在大多数蝙蝠组织中升高,并且基础上,IRFs 有助于 I 型 IFN 配体的表达和干扰素调节基因(IRG)的高表达。CRISPR 敲除(KO)细胞中的 IRF1/3/7 表明,在 IFN 配体信号依赖性和在很大程度上独立的方式下,每个 IRF 影响不同的基因亚群。作为先天免疫的主要调节剂,IRFs 控制 IRG 反应的动力学和维持,并在对甲型流感病毒(IAV)、单纯疱疹病毒 1(HSV-1)、梅拉卡病毒/蝙蝠正粘病毒 3 梅拉卡(PRV3M)和中东呼吸综合征相关冠状病毒(MERS-CoV)感染的反应中发挥重要作用。与人类相比,蝙蝠中的差异表达突出了基础 IRF 表达在病毒反应中的关键作用,以及在蝙蝠免疫细胞发育中的潜在作用,这与人类生物学中 IRF 功能相关。