Ogawa Yohsuke, Sugiura Keita, Kato Kentaro, Tohya Yukinobu, Akashi Hiroomi
National Institute of Animal Health, 3-1-1 Kannondai, Tsukuba, Ibaraki 305-0856, Japan.
Department of Veterinary Microbiology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan.
J Gen Virol. 2007 Dec;88(Pt 12):3385-3390. doi: 10.1099/vir.0.83173-0.
Reverse-genetic systems are often used to study different aspects of the viral life cycle. To date, three rescue systems have been developed for the family Bunyaviridae. These systems use T7 RNA polymerase, which is generally used in rescue systems for Mononegavirales. In the present study, we describe a rescue system for Akabane virus (family Bunyaviridae) that uses cDNAs and RNA polymerase I instead of T7 RNA polymerase. The utility of this system was demonstrated by the generation of a mutant with a deletion of the non-structural protein (NSs) on the S RNA segment. These results offer a new option for bunyavirus rescue.
反向遗传系统常用于研究病毒生命周期的不同方面。迄今为止,已为布尼亚病毒科开发了三种拯救系统。这些系统使用T7 RNA聚合酶,该酶通常用于单股负链RNA病毒目病毒的拯救系统。在本研究中,我们描述了一种用于赤羽病毒(布尼亚病毒科)的拯救系统,该系统使用cDNA和RNA聚合酶I而非T7 RNA聚合酶。通过产生一个在S RNA片段上缺失非结构蛋白(NSs)的突变体,证明了该系统的实用性。这些结果为布尼亚病毒的拯救提供了一种新的选择。