Division of Biomedical and Life Sciences, The Lancaster University, Lancaster, United Kingdom.
Front Cell Infect Microbiol. 2020 Nov 24;10:581504. doi: 10.3389/fcimb.2020.581504. eCollection 2020.
Clustered regularly interspaced short palindromic repeats associated protein nuclease 9 (CRISPR-Cas9) technology offers novel approaches to precisely, cost-effectively, and user-friendly edit genomes for a wide array of applications and across multiple disciplines. This methodology can be leveraged to underpin host-virus interactions, elucidate viral gene functions, and to develop recombinant vaccines. The successful utilization of CRISPR/Cas9 in editing viral genomes has paved the way of developing novel and multiplex viral vectored poultry vaccines. Furthermore, CRISPR/Cas9 can be exploited to rectify major limitations of conventional approaches including reversion to virulent form, recombination with field viruses and transgene, and genome instability. This review provides comprehensive analysis of the potential of CRISPR/Cas9 genome editing technique in understanding avian virus-host interactions and developing novel poultry vaccines. Finally, we discuss the simplest and practical aspects of genome editing approaches in generating multivalent recombinant poultry vaccines that conform simultaneous protection against major avian diseases.
成簇规律间隔短回文重复相关蛋白 9(CRISPR-Cas9)技术为广泛的应用和多个学科提供了精确、经济高效和用户友好的编辑基因组的新方法。该方法可用于研究宿主-病毒相互作用、阐明病毒基因功能以及开发重组疫苗。CRISPR/Cas9 在编辑病毒基因组方面的成功应用为开发新型多价病毒载体禽用疫苗铺平了道路。此外,CRISPR/Cas9 可用于纠正传统方法的主要局限性,包括恢复毒力形式、与田间病毒和转基因的重组以及基因组不稳定性。本文全面分析了 CRISPR/Cas9 基因组编辑技术在了解禽病毒-宿主相互作用和开发新型禽用疫苗方面的潜力。最后,我们讨论了在生成符合同时保护主要禽病的多价重组禽用疫苗方面,基因组编辑方法最简单和实用的方面。