Laboratorio de Inmunología. Centro de Biotecnología Acuícola, Departamento de Biología, Facultad de Química y Biología, Universidad de Santiago de Chile, Alameda, 3363, Santiago, Chile.
Laboratorio de Inmunología Comparativa. Centro de Biotecnología Acuícola, Departamento de Biología, Facultad de Química y Biología, Universidad de Santiago de Chile, Alameda, 3363, Santiago, Chile.
Fish Shellfish Immunol. 2022 Dec;131:785-795. doi: 10.1016/j.fsi.2022.10.060. Epub 2022 Oct 30.
In this study, we examined the cytokine immune response against two proteins of infectious pancreatic necrosis virus (IPNV) in rainbow trout (Oncorhynchus mykiss), the virion-associated RNA polymerase VP1 and VP2-Flagellin (VP2-Flg) fusion protein. Since VP1 is not a structural protein, we hypothesize it can induce cellular immunity, an essential mechanism of the antiviral response. At the same time, the fusion construction VP2-Flg could be highly immunogenic due to the presence of the flagellin used as an adjuvant. Fish were immunized with the corresponding antigen in Montanide™, and the gene expression of a set of marker genes of Th1, Th2, and the immune regulatory response was quantified in the head kidney of immunized and control fish. Results indicate that VP1 induced upregulation of ifn-γ, il-12p40c, il-4/13a, il-4/13b2, il-10a, and tgf-β1 in immunized fish. Expression of il-2a did not change in treated fish at the times tested. The antigen-dependent response was analysed by in vitro restimulation of head kidney leukocytes. In this assay, the group of cytokines upregulated after VP1-restimulation was consistent with those upregulated in the head kidney in vivo. Interestingly, VP1 induced il-2a expression after in vitro restimulation. The analysis of sorted lymphocytes showed that the increase of cytokines occurred in CD4-1 T cells suggesting that Th differentiation happens in response to VP1. This is also consistent with the expression of t-bet and gata3, the master regulators for Th1/Th2 differentiation in the kidneys of immunized animals. A different cytokine expression profile was found after VP2-Flg administration, i.e., upregulation occurs for ifn-γ, il-4/13a, il-10a, and tgf-β1, while down-regulation was observed in il-4/13b2 and il-2a. The cytokine response was due to flagellin; only the il-2a effect was dependent upon VP2 in the fusion protein. To the best of our knowledge this study reports for the first-time characteristics of the adaptive immune response induced in response to IPNV VP1 and the fusion protein VP2-Flg in fish. VP1 induces cytokines able to trigger the humoral and cell-mediated immune response in rainbow trout. The analysis of the fish response against VP2-Flg revealed the immunogenic properties of Aeromonas salmonicida flagellin, which can be further tested for adjuvanticity. The novel immunogenic effects of VP1 in rainbow trout open new opportunities for further IPNV vaccine development using this viral protein.
在这项研究中,我们研究了虹鳟鱼(Oncorhynchus mykiss)中传染性胰脏坏死病毒(IPNV)的两种蛋白的细胞因子免疫反应,即病毒相关 RNA 聚合酶 VP1 和 VP2-Flagellin(VP2-Flg)融合蛋白。由于 VP1 不是结构蛋白,我们假设它可以诱导细胞免疫,这是抗病毒反应的必要机制。同时,由于 Flagellin 作为佐剂的存在,融合结构 VP2-Flg 可能具有高度的免疫原性。鱼用 MontanideTM 中的相应抗原免疫,并在免疫和对照鱼的头肾中定量检测一组 Th1、Th2 和免疫调节反应的标记基因的表达。结果表明,VP1 诱导免疫鱼中 ifn-γ、il-12p40c、il-4/13a、il-4/13b2、il-10a 和 tgf-β1 的上调。在测试的时间内,处理过的鱼中 il-2a 的表达没有变化。通过对头肾白细胞的体外再刺激分析抗原依赖性反应。在该测定中,VP1 再刺激后上调的细胞因子组与体内头肾中上调的细胞因子组一致。有趣的是,VP1 在体外再刺激后诱导了 il-2a 的表达。对分选的淋巴细胞的分析表明,细胞因子的增加发生在 CD4-1 T 细胞中,表明 Th 分化是对 VP1 的反应。这也与免疫动物肾脏中 Th1/Th2 分化的主调控因子 t-bet 和 gata3 的表达一致。VP2-Flg 给药后观察到不同的细胞因子表达谱,即 ifn-γ、il-4/13a、il-10a 和 tgf-β1 上调,而 il-4/13b2 和 il-2a 下调。细胞因子反应归因于鞭毛蛋白;只有融合蛋白中 VP2 依赖于 VP2 的 il-2a 效应。据我们所知,本研究首次报道了虹鳟鱼对 IPNV VP1 和融合蛋白 VP2-Flg 诱导的适应性免疫反应的特征。VP1 诱导能够触发虹鳟鱼体液和细胞介导免疫反应的细胞因子。对虹鳟鱼针对 VP2-Flg 的反应分析揭示了鲑鱼气单胞菌鞭毛蛋白的免疫原性,这可以进一步测试其作为佐剂的作用。VP1 在虹鳟鱼中的新免疫效应为使用这种病毒蛋白进一步开发 IPNV 疫苗提供了新的机会。