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对干扰素进化的新见解:斑马鱼II型干扰素可诱导干扰素依赖性基因快速短暂表达并展现出强大的抗病毒活性。

New insights into the evolution of IFNs: zebrafish group II IFNs induce a rapid and transient expression of IFN-dependent genes and display powerful antiviral activities.

作者信息

López-Muñoz Azucena, Roca Francisco J, Meseguer José, Mulero Victoriano

机构信息

Department of Cell Biology and Histology, Faculty of Biology, University of Murcia, Murcia, Spain.

出版信息

J Immunol. 2009 Mar 15;182(6):3440-9. doi: 10.4049/jimmunol.0802528.

DOI:10.4049/jimmunol.0802528
PMID:19265122
Abstract

The IFNs and their receptors have existed in early chordates for approximately 500 million years and represent the early elements in innate and adaptive immunity. Both types I and II IFNs have been discovered in fish, and type I has recently been classified into two groups based on their primary protein sequences. However, the biological activities of fish IFNs and their roles in infection are largely unknown. Using the zebrafish and manageable bacterial (Streptococcus iniae) and viral (spring viremia of carp virus) infection models, we are reporting in this study that zebrafish IFN (zfIFN) gamma failed to induce antiviral and proinflammatory genes when administered in vivo, which correlates with its inability to protect the fish against bacterial and viral infections. We also found that, although both group I (i.e., zfIFN1) and group II zfIFNs (i.e., zfIFN2 and zfIFN3) displayed strong in vivo antiviral activities, only group I zfIFN was able to protect the fish against bacterial infection, which may reflect the different patterns and kinetics of immune-related genes elicited by these two groups of IFNs. Thus, group II zfIFNs induced a rapid and transient expression of antiviral genes, whereas group I zfIFN exerted a slow but more powerful induction of several antiviral and proinflammatory genes. Collectively, our results suggest nonredundant, complementary roles of type I zfIFNs in viral infections and provide evidence for a pivotal role of the recently identified group II IFN of fish in the early stages of viral infections.

摘要

干扰素及其受体在早期脊索动物中已存在约5亿年,是先天性和适应性免疫的早期组成部分。I型和II型干扰素在鱼类中均已被发现,并且I型干扰素最近根据其一级蛋白质序列被分为两组。然而,鱼类干扰素的生物学活性及其在感染中的作用在很大程度上尚不清楚。利用斑马鱼以及可控的细菌(海豚链球菌)和病毒(鲤鱼春季病毒血症病毒)感染模型,我们在本研究中报告,斑马鱼干扰素(zfIFN)γ在体内给药时未能诱导抗病毒和促炎基因,这与其无法保护鱼类免受细菌和病毒感染相关。我们还发现,尽管I组(即zfIFN1)和II组zfIFN(即zfIFN2和zfIFN3)在体内均表现出强大的抗病毒活性,但只有I组zfIFN能够保护鱼类免受细菌感染,这可能反映了这两组干扰素引发的免疫相关基因的不同模式和动力学。因此,II组zfIFN诱导抗病毒基因快速且短暂的表达,而I组zfIFN对几种抗病毒和促炎基因的诱导作用缓慢但更强。总的来说,我们的结果表明I型zfIFN在病毒感染中具有非冗余的互补作用,并为最近发现的鱼类II型干扰素在病毒感染早期的关键作用提供了证据。

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