Lee Chang-Won, Suarez David L
Food Animal Health Research Program,, Ohio Agricultural Research and Development Center, Ohio State University, Wooster, OH, USA.
Methods Mol Biol. 2008;436:99-111. doi: 10.1007/978-1-59745-279-3_12.
Reverse genetics is the creation of a virus from a full-length cDNA copy of the viral genome, referred to as an infectious clone, and is the most powerful genetic tool in modern virology. The generation of influenza A viruses by reverse genetics has lagged mainly due to the inherent technical difficulties of providing a sufficient amount of all eight viral RNAs from cloned cDNA. A breakthrough was made in 1999 by utilizing the cellular enzyme RNA polymerase I for the synthesis of influenza viral RNAs. Although slightly different methods are being used in different laboratories for the rescue of the influenza virus, the basic concept of synthesizing viral RNA using RNA polymerase I remains the same. Coupled with in vitro mutagenesis, reverse genetics can be applied widely to accelerate progress in understanding the influenza virus life cycle, the generation of live-attenuated vaccines, and the use of influenza virus as vaccine and gene delivery vectors.
反向遗传学是通过病毒基因组的全长cDNA拷贝构建病毒,这种cDNA拷贝被称为感染性克隆,它是现代病毒学中最强大的遗传工具。甲型流感病毒通过反向遗传学的产生主要滞后于从克隆的cDNA中提供足够数量的所有八种病毒RNA所固有的技术难题。1999年,通过利用细胞酶RNA聚合酶I合成流感病毒RNA取得了突破。尽管不同实验室在拯救流感病毒时使用的方法略有不同,但使用RNA聚合酶I合成病毒RNA的基本概念是相同的。结合体外诱变,反向遗传学可广泛应用于加速对流感病毒生命周期的理解、减毒活疫苗的产生以及将流感病毒用作疫苗和基因递送载体等方面的进展。