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通过添加分子佐剂DDX41增强基于糖蛋白的病毒性出血性败血症病毒(VHSV)DNA疫苗

Enhancement of glycoprotein-based DNA vaccine for viral hemorrhagic septicemia virus (VHSV) via addition of the molecular adjuvant, DDX41.

作者信息

Lazarte Jassy Mary S, Kim Young Rim, Lee Jung Seok, Im Se Pyeong, Kim Si Won, Jung Jae Wook, Kim Jaesung, Lee Woo Jai, Jung Tae Sung

机构信息

Laboratory of Aquatic Animal Diseases, College of Veterinary Medicine, Gyeongsang National University, Jinju, South Korea.

BluGen Korea, Busan, South Korea.

出版信息

Fish Shellfish Immunol. 2017 Mar;62:356-365. doi: 10.1016/j.fsi.2017.01.031. Epub 2017 Jan 23.

Abstract

The use of molecular adjuvants to improve the immunogenicity of DNA vaccines has been thoroughly studied in recent years. Glycoprotein (G)-based DNA vaccines had been proven to be effective in combating infection against Rhabdovirus (especially infectious hematopoietic necrosis virus, IHNV) in salmonids. DDX41 is a helicase known to induce antiviral and inflammatory responses by inducing a type I IFN innate immune response. To gain more information regarding G-based DNA vaccines in olive flounder (Paralicthys olivaceus), we tried to develop a more efficient G-based DNA vaccine by adding a molecular adjuvant, DDX41. We designed a DNA vaccine in which the VHSV glycoprotein (G-protein) and DDX41 were driven by the EF-1α and CMV promoters, respectively. Olive flounders were intramuscularly immunized with 1 μg of plasmids encoding the G-based DNA vaccine alone (pEF-G), the molecular adjuvant alone (pEF-D), or the vaccine-adjuvant construct (pEF-GD). At two different time points, 15 and 30 days later, the fish were intraperitoneally infected with VHSV (100 μL; 1 × 10 TCID/mL). Our assays revealed that the plasmid constructs showed up-regulated expression of IFN-1 and its associated genes at day 3 post-vaccination in both kidney and spleen samples. Specifically, pEF-GD showed statistically higher expression of immune response genes than pEF-G and pEF-D treated group (p < 0.05/p < 0.001). After VHSV challenge, the fish group treated with pEF-GD showed higher survival rate than the pEF-G treated group, though difference was not statistically significant in the 15 dpv challenged group however in the 30 dpv challenged group, the difference was statistically significant (p < 0.05). Together, these results clearly demonstrate that DDX41 is an effective adjuvant for the G-based DNA vaccine in olive flounder. Our novel findings could facilitate the development of more effective DNA vaccines for the aquaculture industry.

摘要

近年来,人们对使用分子佐剂来提高DNA疫苗的免疫原性进行了深入研究。基于糖蛋白(G)的DNA疫苗已被证明在抵抗鲑科鱼类感染弹状病毒(特别是传染性造血坏死病毒,IHNV)方面有效。DDX41是一种解旋酶,已知通过诱导I型干扰素先天免疫反应来诱导抗病毒和炎症反应。为了获得更多关于牙鲆(Paralicthys olivaceus)中基于G的DNA疫苗的信息,我们试图通过添加分子佐剂DDX41来开发一种更有效的基于G的DNA疫苗。我们设计了一种DNA疫苗,其中VHSV糖蛋白(G蛋白)和DDX41分别由EF-1α和CMV启动子驱动。牙鲆分别肌肉注射1μg单独编码基于G的DNA疫苗的质粒(pEF-G)、单独的分子佐剂(pEF-D)或疫苗-佐剂构建体(pEF-GD)。在两个不同的时间点,即15天和30天后,将鱼腹腔注射VHSV(100μL;1×10 TCID/mL)。我们的检测显示,在接种疫苗后第3天,质粒构建体在肾脏和脾脏样本中均显示出IFN-1及其相关基因的表达上调。具体而言,pEF-GD显示免疫反应基因的表达在统计学上高于pEF-G和pEF-D处理组(p<0.05/p<0.001)。VHSV攻击后,pEF-GD处理组的鱼存活率高于pEF-G处理组,尽管在15 dpv攻击组中差异无统计学意义,但在30 dpv攻击组中,差异具有统计学意义(p<0.05)。总之,这些结果清楚地表明,DDX41是牙鲆中基于G的DNA疫苗的有效佐剂。我们的新发现有助于为水产养殖业开发更有效的DNA疫苗。

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