Li Kai, Liu Yongzhen, Xu Zengkun, Zhang Yu, Yao Yongxiu, Nair Venugopal, Liu Changjun, Zhang Yanping, Gao Yulong, Qi Xiaole, Cui Hongyu, Gao Li, Wang Xiaomei
Avian Immunosuppressive Diseases Division, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin 150069, China.
The Pirbright Institute and UK-China Centre of Excellence for Research on Avian Diseases, Pirbright, Ash Road, Guildford, Surrey GU24 0NF, UK.
Mol Ther Nucleic Acids. 2020 Sep 4;21:343-353. doi: 10.1016/j.omtn.2020.06.009. Epub 2020 Jun 12.
Reticuloendotheliosis virus (REV) is an avian retrovirus that causes an oncogenic, immunosuppressive, and runting-stunting syndrome in avian hosts. The co-infection of REV and Marek's disease virus (MDV), an oncogenic herpesvirus in chickens, further increases disease severity and reduces MDV vaccine efficacy. The clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 system has successfully been used against pathogens in mammalian cells. However, the large size of the CRISPR-Cas9 coding sequences makes its in vivo delivery challenging. Here, following the design of a panel of single-guided RNAs targeting REV, we demonstrate that CRISPR/Cas9 can efficiently mediate the editing of the long terminal repeats of REV, resulting in the inhibition of viral protein expression. The CRISPR-Cas9 system disrupts the integrated proviral genome and provides defense against new viral infection and replication in chicken cells. Moreover, by constructing recombinant MDV carrying CRISPR-Cas9 components using an attenuated MDV vaccine strain as the vector, we efficiently delivered the CRISPR-Cas9 system into chickens, and the MDV-delivered CRISPR-Cas9 drastically reduced REV viral load and significantly diminished REV-associated symptoms. To our knowledge, this is the first study establishing avian retrovirus resistance in chickens utilizing herpesvirus-delivered CRISPR-Cas9, which provides a novel and effective strategy against viral infections.
网状内皮组织增生症病毒(REV)是一种禽逆转录病毒,可在禽类宿主中引发致癌、免疫抑制和生长迟缓综合征。REV与鸡的致癌性疱疹病毒马立克氏病病毒(MDV)共同感染,会进一步加重疾病严重程度并降低MDV疫苗效力。成簇规律间隔短回文重复序列(CRISPR)-Cas9系统已成功用于对抗哺乳动物细胞中的病原体。然而,CRISPR-Cas9编码序列的大尺寸使其体内递送具有挑战性。在此,在设计了一组靶向REV的单向导RNA后,我们证明CRISPR/Cas9可以有效地介导REV长末端重复序列的编辑,从而抑制病毒蛋白表达。CRISPR-Cas9系统破坏整合的前病毒基因组,并为鸡细胞中新的病毒感染和复制提供防御。此外,通过使用减毒MDV疫苗株作为载体构建携带CRISPR-Cas9组件的重组MDV,我们有效地将CRISPR-Cas9系统递送至鸡体内,并且由MDV递送的CRISPR-Cas9大幅降低了REV病毒载量并显著减轻了与REV相关的症状。据我们所知,这是第一项利用疱疹病毒递送的CRISPR-Cas9在鸡中建立禽逆转录病毒抗性的研究,它提供了一种针对病毒感染的新颖且有效的策略。