Pan Qing, Zhang Yu, Liu Aijing, Cui Hongyu, Gao Yulong, Qi Xiaole, Liu Changjun, Zhang Yanping, Li Kai, Gao Li, Wang Xiaomei
State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, China.
Jiangsu Co-innovation Centre for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou University, Yangzhou, China.
Front Microbiol. 2021 Dec 1;12:780978. doi: 10.3389/fmicb.2021.780978. eCollection 2021.
Severe hepatitis-hydropericardium syndrome (HHS) associated with a novel viral genotype, fowl adenovirus 4 (FAdV-4), has emerged and widely spread in China since 2015, causing severe economic losses to the poultry industry. We previously reported that the hexon gene is responsible for pathogenicity and obtained a non-pathogenic hexon-replacement rHN20 strain; however, the lack of information about the non-essential regions for virus replication limits the development of a FAdV-4 vector. This study first established an enhanced green fluorescent protein (EGFP)-indicator virus based on the FAdV-4 reverse genetic technique, effective for batch operations in the virus genome. Based on this, 10 open reading frames (ORFs) at the left end and 13 ORFs at the right end of the novel FAdV-4 genome were deleted separately and identified as non-essential genes for viral replication, providing preliminary insertion sites for foreign genes. To further improve its feasibility as a vaccine vector, seven combinations of ORFs were successfully replaced with EGFP without affecting the immunogenicity of the vector backbone. Finally, a recombinant rHN20-vvIBDV-VP2 strain, expressing the VP2 protein of very virulent infectious bursa disease virus (vvIBDV), was rescued and showed complete protection against FAdV-4 and vvIBDV. Thus, the novel FAdV-4 vector could provide sufficient protection for HHS and efficient exogenous gene delivery. Overall, our findings systemically identified 23 non-essential ORFs for FAdV-4 replication and seven foreign gene insertion regions, providing valuable information for an in-depth understanding of the novel FAdV-4 pathogenesis and development of multivalent vaccines.
自2015年以来,与一种新型病毒基因型——禽腺病毒4型(FAdV - 4)相关的严重肝炎 - 心包积水综合征(HHS)在中国出现并广泛传播,给家禽业造成了严重的经济损失。我们之前报道过六邻体基因与致病性有关,并获得了一种无致病性的六邻体替换rHN20株;然而,关于病毒复制非必需区域的信息缺乏限制了FAdV - 4载体的开发。本研究首先基于FAdV - 4反向遗传技术建立了一种增强型绿色荧光蛋白(EGFP)指示病毒,可有效用于病毒基因组的批量操作。在此基础上,分别删除了新型FAdV - 4基因组左端的10个开放阅读框(ORF)和右端的13个ORF,并确定它们为病毒复制的非必需基因,为外源基因提供了初步插入位点。为进一步提高其作为疫苗载体的可行性,成功地用EGFP替换了7种ORF组合,且不影响载体骨架的免疫原性。最后,拯救出了表达超强毒传染性法氏囊病病毒(vvIBDV)VP2蛋白的重组rHN20 - vvIBDV - VP2株,该株对FAdV - 4和vvIBDV均显示出完全保护作用。因此,新型FAdV - 4载体可为HHS提供充分保护并实现高效的外源基因递送。总体而言,我们的研究结果系统地鉴定了23个FAdV - 4复制的非必需ORF和7个外源基因插入区域,为深入了解新型FAdV - 4发病机制和开发多价疫苗提供了有价值的信息。