Boyer J C, Zaccomer B, Haenni A L
Institut Jacques Monod, Tour, Paris, France.
J Gen Virol. 1993 Sep;74 ( Pt 9):1911-7. doi: 10.1099/0022-1317-74-9-1911.
We describe here a convenient and efficient system for studying turnip yellow mosaic virus (TYMV) replication in leaf protoplasts. Inoculation of rapeseed (Brassica napus) or Chinese cabbage (B. sinensis) protoplasts was achieved via electroporation, and sensitive detection of viral RNA products was performed by Northern blot analyses using a non-radioactive digoxigenin-labelled cDNA probe. Virus replication was detected when 1.5 x 10(6) rapeseed protoplasts were inoculated with 20 ng of TYMV RNA. Electrotransfection of TYMV RNA was more efficient in rapeseed than in Chinese cabbage protoplasts, and gave somewhat higher signals than those of TYMV virions. TYMV RNA appeared to replicate equally well whether the protoplasts were incubated in the dark or under constant light.
我们在此描述了一种用于研究芜菁黄花叶病毒(TYMV)在叶原生质体中复制的便捷高效系统。通过电穿孔法对油菜(甘蓝型油菜)或大白菜(小白菜)原生质体进行接种,并使用非放射性地高辛标记的cDNA探针通过Northern印迹分析对病毒RNA产物进行灵敏检测。当用20 ng的TYMV RNA接种1.5×10⁶个油菜原生质体时,可检测到病毒复制。TYMV RNA的电转染在油菜原生质体中比在大白菜原生质体中更高效,并且产生的信号比TYMV病毒粒子的信号略高。无论原生质体是在黑暗中还是在持续光照下培养,TYMV RNA似乎都能同样良好地复制。