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Duck Enteritis Virus Glycoprotein D and B DNA Vaccines Induce Immune Responses and Immunoprotection in Pekin Ducks

机译:鸭肠炎病毒糖蛋白D和B DNA疫苗可诱导北京鸭的免疫反应和免疫保护作用

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摘要

DNA vaccine is a promising strategy for protection against virus infection. However, little is known on the efficacy of vaccination with two plasmids for expressing the glycoprotein D (gD) and glycoprotein B (gB) of duck enteritis virus (DEV) in inducing immune response and immunoprotection against virulent virus infection in Pekin ducks. In this study, two eukaryotic expressing plasmids of pcDNA3.1-gB and pcDNA3.1-gD were constructed. Following transfection, the gB and gD expressions in DF1 cells were detected. Groups of ducks were vaccinated with pcDNA3.1-gB and/or pcDNA3.1-gD, and boosted with the same vaccine on day 14 post primary vaccination. We found that intramuscular vaccinations with pcDNA3.1-gB and/or pcDNA3.1-gD, but not control plasmid, stimulated a high frequency of CD4+ and CD8+ T cells in Pekin ducks, particularly with both plasmids. Similarly, vaccination with these plasmids, particularly with both plasmids, promoted higher levels of neutralization antibodies against DEV in Pekin ducks. More importantly, vaccination with both plasmids significantly reduced the virulent DEV-induced mortality in Pekin ducks. Our data indicated that vaccination with plasmids for expressing both gB and gD induced potent cellular and humoral immunity against DEV in Pekin ducks. Therefore, this vaccination strategy may be used for the prevention of DEV infection in Pekin ducks.
机译:DNA疫苗是防止病毒感染的一种有前途的策略。然而,关于两种表达鸭肠炎病毒(DEV)的糖蛋白D(gD)和糖蛋白B(gB)的质粒的疫苗接种在诱导免疫应答和针对强毒鸭子感染中的强病毒感染的免疫保护方面的功效鲜为人知。在这项研究中,构建了两个pcDNA3.1-gB和pcDNA3.1-gD真核表达质粒。转染后,检测到DF1细胞中的gB和gD表达。用pcDNA3.1-gB和/或pcDNA3.1-gD给各组鸭子接种疫苗,并在初次接种后第14天用相同的疫苗加强免疫。我们发现,用pcDNA3.1-gB和/或pcDNA3.1-gD而不是对照质粒进行肌内接种可刺激高频率的CD4 + 和CD8 + T北京鸭中的细胞,特别是两种质粒。类似地,用这些质粒,特别是用两种质粒的疫苗接种,促进了北京鸭中针对DEV的中和抗体的更高水平。更重要的是,两种质粒的疫苗接种都大大降低了北京鸭低毒的DEV致死率。我们的数据表明,用表达gB和gD的质粒进行疫苗接种可诱导北京鸭对DEV产生有效的细胞和体液免疫。因此,该疫苗接种策略可用于预防北京烤鸭的DEV感染。

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