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重组鸭肠炎病毒载体二价疫苗有效预防鸭甲型肝炎病毒感染鸭

Recombinant Duck Enteritis Virus-Vectored Bivalent Vaccine Effectively Protects Against Duck Hepatitis A Virus Infection in Ducks.

作者信息

Yang Fuchun, Liu Peng, Li Xiaohan, Liu Rui, Gao Li, Cui Hongyu, Zhang Yanping, Liu Changjun, Qi Xiaole, Pan Qing, Liu Aijing, Wang Xiaomei, Gao Yulong, Li Kai

机构信息

Avian Immunosuppressive Diseases Division, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, China.

出版信息

Front Microbiol. 2021 Dec 22;12:813010. doi: 10.3389/fmicb.2021.813010. eCollection 2021.

Abstract

Duck enteritis virus (DEV) and duck hepatitis A virus (DHAV) are prevalent duck pathogens, causing significant economic losses in the duck industry annually. Using a fosmid-based rescue system, we generated two DEV recombinants, rDEV-UL26/27-P13C and rDEV-US7/8-P13C, in which the P1 and 3C genes from DHAV type 3 (DHAV-3) were inserted into the DEV genome between genes UL26 and UL27 or genes US7 and US8. We inserted a self-cleaving 2A-element between P1 and 3C, allowing the production of both proteins from a single open reading frame. P1 and 3C were simultaneously expressed in infected chicken embryo fibroblasts, with no difference in growth kinetics between cells infected with the recombinant viruses and those infected with the parent DEV. Both recombinant viruses induced neutralizing antibodies against DHAV-3 and DEV in ducks. A single dose of the recombinant viruses induced solid protection against lethal DEV challenge and completely prevented DHAV-3 infection as early as 7 days post-vaccination. These recombinant P1- and 3C-expressing DEVs provide potential bivalent vaccines against DEV and DHAV-3 infection in ducks.

摘要

鸭肠炎病毒(DEV)和鸭甲型肝炎病毒(DHAV)是鸭群中常见的病原体,每年给养鸭业造成重大经济损失。我们利用基于fosmid的拯救系统构建了两种DEV重组体,即rDEV-UL26/27-P13C和rDEV-US7/8-P13C,其中来自3型鸭甲型肝炎病毒(DHAV-3)的P1和3C基因被插入到DEV基因组中UL26和UL27基因之间或US7和US8基因之间。我们在P1和3C之间插入了一个自我切割的2A元件,使得能够从单个开放阅读框中产生这两种蛋白质。P1和3C在感染的鸡胚成纤维细胞中同时表达,感染重组病毒的细胞与感染亲本DEV的细胞在生长动力学上没有差异。两种重组病毒均能在鸭体内诱导产生针对DHAV-3和DEV的中和抗体。单剂量的重组病毒可诱导对致死性DEV攻击的坚实保护,并早在接种疫苗后7天就完全预防DHAV-3感染。这些表达重组P1和3C的DEV为鸭群预防DEV和DHAV-3感染提供了潜在的二价疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ffc/8727602/c224974eb273/fmicb-12-813010-g001.jpg

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