Neumann G, Kawaoka Y
Department of Pathobiological Sciences, School of Veterinary Medicine, Madison, Wisconsin 53706, USA.
Virology. 2001 Sep 1;287(2):243-50. doi: 10.1006/viro.2001.1008.
Reverse genetics of negative-sense RNA viruses, which enables one to generate virus entirely from cloned cDNA, has progressed rapidly over the past decade. However, despite the relative ease with which nonsegmented negative-sense RNA viruses can now be produced from plasmids, the ability to generate viruses with segmented genomes has lagged considerably, largely because of the inherent technical difficulties in providing all viral RNAs and proteins from cloned cDNA. A breakthrough in reverse genetics technology in the influenza virus field came in 1999, when we (Neumann et al., 1999, Proc. Natl. Acad. Sci. USA 96, 9345-9350) and others (Fodor et al., 1999, J. Virol. 73, 9679-9682) exploited a new approach to viral RNA production. In this review, we discuss the background for this advance, the systems that are now available for the generation of influenza viruses, and the implications of these developments for the future of virus research.
负链RNA病毒的反向遗传学技术能使人们完全从克隆的cDNA中产生病毒,在过去十年中取得了迅速进展。然而,尽管现在从质粒中产生非节段负链RNA病毒相对容易,但产生具有节段基因组的病毒的能力却大大滞后,这主要是因为从克隆的cDNA中提供所有病毒RNA和蛋白质存在固有的技术困难。1999年,流感病毒领域的反向遗传学技术取得了突破,当时我们(Neumann等人,1999年,《美国国家科学院院刊》96卷,9345 - 9350页)和其他人(Fodor等人,1999年,《病毒学杂志》73卷,9679 - 9682页)采用了一种新的病毒RNA生产方法。在这篇综述中,我们讨论了这一进展的背景、现在可用于产生流感病毒的系统,以及这些进展对病毒研究未来的影响。