Cheng Benson Y H, Ortiz-Riaño Emilio, de la Torre Juan Carlos, Martínez-Sobrido Luis
Department of Microbiology and Immunology, University of Rochester School of Medicine and Dentistry, USA.
J Vis Exp. 2013 Aug 1(78):50662. doi: 10.3791/50662.
The development and implementation of arenavirus reverse genetics represents a significant breakthrough in the arenavirus field. The use of cell-based arenavirus minigenome systems together with the ability to generate recombinant infectious arenaviruses with predetermined mutations in their genomes has facilitated the investigation of the contribution of viral determinants to the different steps of the arenavirus life cycle, as well as virus-host interactions and mechanisms of arenavirus pathogenesis. In addition, the development of trisegmented arenaviruses has permitted the use of the arenavirus genome to express additional foreign genes of interest, thus opening the possibility of arenavirus-based vaccine vector applications. Likewise, the development of single-cycle infectious arenaviruses capable of expressing reporter genes provides a new experimental tool to improve the safety of research involving highly pathogenic human arenaviruses. The generation of recombinant arenaviruses using plasmid-based reverse genetics techniques has so far relied on the use of rodent cell lines, which poses some barriers for the development of Food and Drug Administration (FDA)-licensed vaccine or vaccine vectors. To overcome this obstacle, we describe here the efficient generation of recombinant arenaviruses in FDA-approved Vero cells.
沙粒病毒反向遗传学的发展与应用是沙粒病毒领域的一项重大突破。基于细胞的沙粒病毒微型基因组系统的应用,以及在基因组中产生具有预定突变的重组感染性沙粒病毒的能力,有助于研究病毒决定因素在沙粒病毒生命周期不同阶段的作用,以及病毒与宿主的相互作用和沙粒病毒发病机制。此外,三段式沙粒病毒的开发使得利用沙粒病毒基因组表达其他感兴趣的外源基因成为可能,从而开启了基于沙粒病毒的疫苗载体应用的可能性。同样,能够表达报告基因的单循环感染性沙粒病毒的开发提供了一种新的实验工具,以提高涉及高致病性人类沙粒病毒研究的安全性。迄今为止,使用基于质粒的反向遗传学技术产生重组沙粒病毒依赖于啮齿动物细胞系的使用,这为美国食品药品监督管理局(FDA)批准的疫苗或疫苗载体的开发带来了一些障碍。为克服这一障碍,我们在此描述了在FDA批准的Vero细胞中高效产生重组沙粒病毒的方法。