A novel fiber-2-edited live attenuated vaccine candidate against the highly pathogenic serotype 4 fowl adenovirus

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作者
Quan Xie
Shiya Cao
Wei Zhang
Weikang Wang
Luyuan Li
Qiuqi Kan
Hui Fu
Tuoyu Geng
Tuofan Li
Zhimin Wan
Wei Gao
Hongxia Shao
Aijian Qin
Jianqiang Ye
机构
[1] Yangzhou University,Key Laboratory of Jiangsu Preventive Veterinary Medicine, Key Laboratory for Avian Preventive Medicine, Ministry of Education, College of Veterinary Medicine
[2] Jiangsu Co-Innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses,Joint International Research Laboratory of Agriculture and Agri
[3] Yangzhou University,Product Safety, the Ministry of Education of China
[4] Yangzhou University,Institute of Agricultural Science and Technology Development
[5] Sinopharm Yangzhou VAC Biological Engineering Co.Ltd,College of Animal Science and Technology
[6] Yangzhou University,undefined
来源
关键词
FAdV-4; CRISPR/Cas9; Recombinant virus; Attenuation; Vaccine candidate;
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摘要
Recently, the outbreaks of hydropericardium-hepatitis syndrome (HHS) caused by the highly pathogenic fowl adenovirus serotype 4 (FAdV-4) have resulted in huge economic losses to the poultry industry globally. Although several inactivated or subunit vaccines have been developed against FAdV-4, live-attenuated vaccines for FAdV-4 are rarely reported. In this study, a recombinant virus FA4-EGFP expressing EGFP-Fiber-2 fusion protein was generated by the CRISPR/Cas9 technique. Although FA4-EGFP shows slightly lower replication ability than the wild type (WT) FAdV-4, FA4-EGFP was significantly attenuated in vivo compared with the WT FAdV-4. Chickens infected with FA4-EGFP did not show any clinical signs, and all survived to 14 day post-infection (dpi), whereas those infected with FAdV-4 showed severe clinical signs with HHS and all died at 4 dpi. Besides, the inoculation of FA4-EGFP in chickens provided efficient protection against lethal challenge with FAdV-4. Compared with an inactivated vaccine, FA4-EGFP induced neutralizing antibodies with higher titers earlier. All these data not only provide a live-attenuated vaccine candidate against the highly pathogenic FAdV-4 but also give a potential insertion site for developing FAdV-4-based vaccine vectors for delivering foreign antigens.
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