Almazán Fernando, Sola Isabel, Zuñiga Sonia, Marquez-Jurado Silvia, Morales Lucia, Becares Martina, Enjuanes Luis
Department of Molecular and Cell Biology. Centro Nacional de Biotecnología (CNB-CSIC), Campus Universidad Autónoma de Madrid, C/ Darwin 3, Cantoblanco, 28049 Madrid, Spain.
Department of Molecular and Cell Biology. Centro Nacional de Biotecnología (CNB-CSIC), Campus Universidad Autónoma de Madrid, C/ Darwin 3, Cantoblanco, 28049 Madrid, Spain.
Virus Res. 2014 Dec 19;194:67-75. doi: 10.1016/j.virusres.2014.09.006. Epub 2014 Sep 26.
Coronaviruses (CoVs) infect humans and many animal species, and are associated with respiratory, enteric, hepatic, and central nervous system diseases. The large size of the CoV genome and the instability of some CoV replicase gene sequences during its propagation in bacteria, represent serious obstacles for the development of reverse genetic systems similar to those used for smaller positive sense RNA viruses. To overcome these limitations, several alternatives to more conventional plasmid-based approaches have been established in the last 13 years. In this report, we briefly review and discuss the different reverse genetic systems developed for CoVs, paying special attention to the severe acute respiratory syndrome CoV (SARS-CoV).
冠状病毒(CoVs)可感染人类和许多动物物种,并与呼吸道、肠道、肝脏及中枢神经系统疾病相关。冠状病毒基因组规模庞大,且其某些复制酶基因序列在细菌中繁殖时不稳定,这对开发类似于用于较小正链RNA病毒的反向遗传系统构成了严重障碍。为克服这些限制,在过去13年里已建立了几种不同于更传统基于质粒方法的替代方法。在本报告中,我们简要回顾并讨论了针对冠状病毒开发的不同反向遗传系统,特别关注严重急性呼吸综合征冠状病毒(SARS-CoV)。