Laboratory of Pathology and Immunology of Aquatic Animals, KLMME, Ocean University of China, 5 Yushan Road, Qingdao, 266003, China.
Laboratory of Pathology and Immunology of Aquatic Animals, KLMME, Ocean University of China, 5 Yushan Road, Qingdao, 266003, China; Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, No. 1 Wenhai Road, Aoshanwei Town, Qingdao, 266071, China.
Fish Shellfish Immunol. 2019 Oct;93:1018-1027. doi: 10.1016/j.fsi.2019.08.052. Epub 2019 Aug 22.
In our previous study, a DNA plasmid encoding the VAA gene of Vibrio anguillarum was constructed and demonstrated to confer moderated protection against V. anguillarum challenge. Here, a bicistronic DNA vaccine (pVAA-IRES-IL2), co-expressing the VAA gene of V. anguillarum and Interleukin-2 (IL2) gene of flounder, was constructed to increase the protective efficacy of VAA DNA vaccine. The potential of pVAA-IRES-IL2 to express both VAA and IL2 in transfected HINAE cell lines was confirmed by immunofluorescence assay. Further, the variation of sIgM, CD4-1, CD4-2 lymphocytes and production of VAA-specific antibodies in flounder, which was intramuscularly immunized with three DNA plasmids (pIRES, pVAA-IRES, pVAA-IRES-IL2), were investigated, respectively. The bacterial burden and relative percentage survival (RPS) of flounder exposed to V. anguillarum infection were both analyzed to evaluate the efficacy of bicistronic DNA plasmid. Our results revealed that the percentages of sIgM, CD4-1, CD4-2 lymphocytes and antibodies specific to VAA were remarkably increased in pVAA-IRES or pVAA-IRES-IL2 immunized fish. Moreover, the co-expression of IL2 enhanced the immune response in response to VAA DNA vaccination, as shown by the higher percentages of sIgM, CD4-1, CD4-2 lymphocytes and production of specific antibody. Importantly, the RPS in pVAA-IRES-IL2 and pVAA-IRES groups reached 64.1% and 51.3%, respectively, when compared with the 97.5% cumulative mortality in pIRES group. Furthermore, the number of V. anguillarum in liver, spleen and kidney of pVAA-IRES or pVAA-IRES-IL2 immunized flounder after V. anguillarum challenge was significantly reduced, as compared to that in pIRES group. These suggest that the bicistronic DNA vaccine can be an effective immunization strategy in inducing immune response against V. anguillarum infection and IL2 has the potential as the adjuvant for VAA DNA vaccine.
在我们之前的研究中,构建了一种编码鳗弧菌 VAA 基因的 DNA 质粒,并证明其能对鳗弧菌的攻击提供适度的保护。在这里,构建了一种双顺反子 DNA 疫苗(pVAA-IRES-IL2),共同表达鳗弧菌的 VAA 基因和牙鲆的白细胞介素 2(IL2)基因,以提高 VAA DNA 疫苗的保护效果。通过免疫荧光分析证实了 pVAA-IRES-IL2 在转染的 HINAE 细胞系中表达 VAA 和 IL2 的潜能。此外,通过肌肉内免疫三种 DNA 质粒(pIRES、pVAA-IRES 和 pVAA-IRES-IL2),分别研究了牙鲆的 sIgM、CD4-1、CD4-2 淋巴细胞的变化以及鳗弧菌特异性抗体的产生。分析了牙鲆暴露于鳗弧菌感染后的细菌负荷和相对存活率(RPS),以评估双顺反子 DNA 质粒的效果。我们的结果表明,在 pVAA-IRES 或 pVAA-IRES-IL2 免疫的鱼中,sIgM、CD4-1、CD4-2 淋巴细胞和针对 VAA 的抗体的百分比显著增加。此外,IL2 的共表达增强了对 VAA DNA 疫苗接种的免疫反应,表现为 sIgM、CD4-1、CD4-2 淋巴细胞和特异性抗体的产生百分比更高。重要的是,与 pIRES 组 97.5%的累积死亡率相比,pVAA-IRES-IL2 和 pVAA-IRES 组的 RPS 分别达到 64.1%和 51.3%。此外,在鳗弧菌攻毒后,pVAA-IRES 或 pVAA-IRES-IL2 免疫的牙鲆的肝、脾和肾中的鳗弧菌数量与 pIRES 组相比显著减少。这表明双顺反子 DNA 疫苗可以作为一种有效的免疫策略,诱导对鳗弧菌感染的免疫反应,而 IL2 有可能作为 VAA DNA 疫苗的佐剂。