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IFNb 在鲤鱼的固有免疫反应中作为一种抗病毒细胞因子,发挥着重要作用。

IFNb of black carp functions importantly in host innate immune response as an antiviral cytokine.

机构信息

State Key Laboratory of Developmental Biology of Freshwater Fish, College of Life Science, Hunan Normal University, Changsha, 410081, China.

Department of Pediatrics, The Second Xiangya Hospital, Central South University, Changsha, 410011, China.

出版信息

Fish Shellfish Immunol. 2018 Mar;74:1-9. doi: 10.1016/j.fsi.2017.12.049. Epub 2017 Dec 25.

DOI:10.1016/j.fsi.2017.12.049
PMID:29284145
Abstract

Type I interferons (IFN-Is) play an important role in the antiviral immune response in teleost fishes. In this study, one type I interferon (bcIFNb) from black carp (Mylopharyngodon piceus) has been cloned and characterized. The full-length cDNA of bcIFNb gene consists of 806 nucleotides and the predicted bcIFNb protein contains 188 amino acids. Basing on the cysteine number and evolutionary position, bcIFNb was classified into group II type I IFN. q-PCR analysis demonstrated that bcIFNb mRNA level varied in vivo and ex vivo in response to different stimuli. bcIFNb was detected in both the whole cell lysate and the supernatant media of HEK293T cells or EPC cells transfected with bcIFNb through immunoblot assay. IFN stimulated genes (ISGs) were greatly upregulated when the host cells were treated with the bcIFNb-containing conditioned media. EPC cells showed greatly enhanced antiviral ability when the cells were transfected with bcIFNb or treated with the bcIFNb-containing conditioned media before GCRV or SVCV infection. Glycosidase digestion analysis determined that bcIFNb was modified with N-linked glycosylation, which occurred on the Asn (N) of 92 site of this cytokine. The un-glycosylated mutant bcIFNb-N92Q presented the similar antiviral ability as that of wild type bcIFNb, which demonstrated that N-linked glycosylation did not contribute directly to the antiviral property of this fish cytokine.

摘要

I 型干扰素(IFN-Is)在鱼类抗病毒免疫反应中发挥重要作用。本研究克隆并鉴定了草鱼(Mylopharyngodon piceus)的 I 型干扰素(bcIFNb)。bcIFNb 基因全长 cDNA 由 806 个核苷酸组成,预测的 bcIFNb 蛋白含有 188 个氨基酸。基于半胱氨酸数量和进化位置,bcIFNb 被归类为 II 型 I 型 IFN。q-PCR 分析表明,bcIFNb mRNA 水平在体内和体外对不同刺激表现出变化。通过免疫印迹分析,在转染 bcIFNb 的 HEK293T 细胞或 EPC 细胞的全细胞裂解液和上清液中均检测到 bcIFNb。当宿主细胞用含有 bcIFNb 的条件培养基处理时,IFN 刺激基因(ISGs)显著上调。当细胞转染 bcIFNb 或在 GCRV 或 SVCV 感染前用含有 bcIFNb 的条件培养基处理时,EPC 细胞显示出增强的抗病毒能力。糖苷酶消化分析确定 bcIFNb 经过 N 连接糖基化修饰,该修饰发生在细胞因子的 92 位天冬酰胺(N)上。未经糖基化修饰的突变体 bcIFNb-N92Q 表现出与野生型 bcIFNb 相似的抗病毒能力,这表明 N 连接糖基化并非直接导致这种鱼类细胞因子的抗病毒特性。

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