Key Laboratory of Jiangsu Preventive Veterinary Medicine, Key Laboratory for Avian Preventive Medicine, Ministry of Education, College of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Jiangsu Co-Innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou, 225009, Jiangsu, China.
Vet Res. 2021 Feb 27;52(1):35. doi: 10.1186/s13567-021-00907-z.
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.
最近,由高致病性禽腺病毒血清型 4(FAdV-4)引起的心包积液-肝炎综合征(HHS)的爆发,给全球家禽业造成了巨大的经济损失。尽管已经开发出几种针对 FAdV-4 的灭活或亚单位疫苗,但很少有针对 FAdV-4 的活疫苗报道。在本研究中,通过 CRISPR/Cas9 技术生成了表达 EGFP-Fiber-2 融合蛋白的重组病毒 FA4-EGFP。虽然 FA4-EGFP 的复制能力略低于野生型(WT)FAdV-4,但与 WT FAdV-4 相比,FA4-EGFP 在体内明显减毒。感染 FA4-EGFP 的鸡没有出现任何临床症状,并且在感染后 14 天(dpi)全部存活,而感染 FAdV-4 的鸡出现严重的 HHS 临床症状,并且在 4 dpi 全部死亡。此外,FA4-EGFP 接种可有效预防 FAdV-4 的致死性攻毒。与灭活疫苗相比,FA4-EGFP 更早诱导出具有更高滴度的中和抗体。所有这些数据不仅为高致病性 FAdV-4 提供了一种活疫苗候选物,而且为开发用于传递外源抗原的基于 FAdV-4 的疫苗载体提供了一个潜在的插入位点。