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一种针对高致病性血清型 4 禽腺病毒的新型纤维-2 编辑活减毒疫苗候选物。

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

机构信息

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.

出版信息

Vet Res. 2021 Feb 27;52(1):35. doi: 10.1186/s13567-021-00907-z.

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cc4/7912893/f2e18a16461c/13567_2021_907_Fig1_HTML.jpg

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