Thao Tran Thi Nhu, Labroussaa Fabien, Ebert Nadine, Jores Joerg, Thiel Volker
Institute of Virology and Immunology IVI, Bern, Switzerland.
Department of Infectious Diseases and Pathobiology, Vetsuisse Faculty, University of Bern, Bern, Switzerland.
Methods Mol Biol. 2020;2203:167-184. doi: 10.1007/978-1-0716-0900-2_13.
The Escherichia coli and vaccinia virus-based reverse genetics systems have been widely applied for the manipulation and engineering of coronavirus genomes. These systems, however, present several limitations and are sometimes difficult to establish in a timely manner for (re-)emerging viruses. In this chapter, we present a new universal reverse genetics platform for the assembly and engineering of infectious full-length cDNAs using yeast-based transformation-associated recombination cloning. This novel assembly method not only results in stable coronavirus infectious full-length cDNAs cloned in the yeast Saccharomyces cerevisiae but also fosters and accelerates the manipulation of their genomes. Such a platform is widely applicable for the scientific community, as it requires no specific equipment and can be performed in a standard laboratory setting. The protocol described can be easily adapted to virtually all known or emerging coronaviruses, such as Middle East respiratory syndrome coronavirus (MERS-CoV).
基于大肠杆菌和痘苗病毒的反向遗传学系统已被广泛应用于冠状病毒基因组的操作和工程改造。然而,这些系统存在一些局限性,对于新出现的(再出现的)病毒,有时难以及时建立。在本章中,我们介绍了一种新的通用反向遗传学平台,该平台利用基于酵母的转化相关重组克隆技术来组装和改造感染性全长cDNA。这种新颖的组装方法不仅能在酿酒酵母中稳定克隆冠状病毒感染性全长cDNA,还能促进和加速其基因组的操作。这样一个平台对科学界具有广泛适用性,因为它不需要特定设备,并且可以在标准实验室环境中进行。所描述的方案可以很容易地适用于几乎所有已知或新出现的冠状病毒,如中东呼吸综合征冠状病毒(MERS-CoV)。