Shenzhen Institute of Guangdong Ocean University, Shenzhen, 518120, China; State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China; College of Fishery, Guangdong Ocean University, Zhanjiang, 524025, China; Guangdong Provincial Engineering Research Center for Aquatic Animal Health Assessment, And Shenzhen Public Service Platform for Evaluation of Marine Economic Animal Seedings, Shenzhen, 518120, China.
Shenzhen Institute of Guangdong Ocean University, Shenzhen, 518120, China; College of Fishery, Guangdong Ocean University, Zhanjiang, 524025, China; Guangdong Provincial Engineering Research Center for Aquatic Animal Health Assessment, And Shenzhen Public Service Platform for Evaluation of Marine Economic Animal Seedings, Shenzhen, 518120, China.
Fish Shellfish Immunol. 2021 May;112:74-80. doi: 10.1016/j.fsi.2021.02.016. Epub 2021 Mar 2.
The dsRNA-activated protein kinase R (PKR) is one of key antiviral effectors induced by interferons (IFNs), and its functions are largely unknown in tilapia, an important commercial fish species suffering from several viral infectious diseases. In the present study, a PKR gene named On-PKR was identified and cloned from Nile tilapia, Oreochromis niloticus. On-PKR gene was constitutively expressed in all tissues examined, with the highest expression level observed in head kidney and liver, and was rapidly induced in all organs/tissues tested following the stimulation of poly(I:C). Importantly, the expression of On-PKR is induced by group I and group II IFNs with distinct induction kinetics in vivo: group I IFN elicits a relative delayed but sustained induction of On-PKR, whereas group II IFN triggers a rapid and transient expression of On-PKR. Moreover, the overexpression of On-PKR has been proven to inhibit the protein translation and virus replication in fish cells. The present study thus contributes to a better understanding of the functions of antiviral effectors in tilapia, and may provide clues for the prevention and therapy of viral diseases in fish.
双链 RNA 激活的蛋白激酶 R (PKR) 是干扰素 (IFNs) 诱导的关键抗病毒效应因子之一,但其在罗非鱼中的功能尚不清楚,罗非鱼是一种重要的商业鱼类,患有多种病毒性传染病。本研究从尼罗罗非鱼 (Oreochromis niloticus) 中鉴定并克隆了一种 PKR 基因,命名为 On-PKR。On-PKR 基因在所有检测到的组织中均持续表达,在头肾和肝脏中表达水平最高,在用 poly(I:C) 刺激后,所有检测到的器官/组织中均迅速诱导表达。重要的是,On-PKR 的表达受 I 型和 II 型干扰素的诱导,体内诱导动力学不同:I 型干扰素引起 On-PKR 的相对延迟但持续诱导,而 II 型干扰素则触发 On-PKR 的快速和短暂表达。此外,On-PKR 的过表达已被证明可抑制鱼类细胞中的蛋白质翻译和病毒复制。本研究有助于更好地了解抗病毒效应因子在罗非鱼中的功能,并可能为鱼类病毒性疾病的预防和治疗提供线索。