| Literature DB >> 33640033 |
Quan Xie1,2,3,4, Shiya Cao1,2,3,4, Wei Zhang5, Weikang Wang1,2,3,4, Luyuan Li1,2,3,4, Qiuqi Kan1,2,3,4, Hui Fu1,2,3,4, Tuoyu Geng6, Tuofan Li1,2,3,4, Zhimin Wan1,2,3,4, Wei Gao1,2,3,4, Hongxia Shao1,2,3,4, Aijian Qin1,2,3,4, Jianqiang Ye7,8,9,10.
Abstract
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.Entities:
Keywords: Attenuation; CRISPR/Cas9; FAdV-4; Recombinant virus; Vaccine candidate
Year: 2021 PMID: 33640033 PMCID: PMC7912893 DOI: 10.1186/s13567-021-00907-z
Source DB: PubMed Journal: Vet Res ISSN: 0928-4249 Impact factor: 3.683