Coutts R H, Wood K R
Arch Virol. 1976;52(1-2):59-69. doi: 10.1007/BF01317865.
Protoplasts from the first leaf mesophyll of cucumber plants were isolated by an 18 hours combined petinase/cellulase treatment. Conditions favouring the infection of these protoplasts with tobacco mosaic virus (TMV), and the accumulation of infective virus up to 96 hours after inoculation have been studied. Infection of approximately 5--10 per cent of the protoplats, revealed by indirect fluorescent antibody staining, was achieved by pre-treatment of the cells in 0.01 M citrate-buffered mannitol (CBM), pH 5.2 with 2 mug/ml poly-L-ornithine followed by centrifugation and direct resuspension of the cells in the same mixture together with 2 to 4 mug/ml TMV. Higher concentrations of the polycation and buffer were toxic to the protoplasts. Under the best conditions, virus yields of approximately 10-20 mug TMV/10(6) protoplasts were attained, while after 72 hours incubation, significant amounts of virus could often be recovered from the incubation medium. Addition of actinomycin D to cultures of protoplasts 2 hours post-inoculation partially inhibited development of infectivity.
通过18小时的果胶酶/纤维素酶联合处理,分离出黄瓜植株第一片叶叶肉的原生质体。研究了有利于这些原生质体被烟草花叶病毒(TMV)感染以及接种后96小时内感染性病毒积累的条件。通过间接荧光抗体染色显示,约5%-10%的原生质体被感染,方法是将细胞在pH 5.2的0.01M柠檬酸盐缓冲甘露醇(CBM)中用2μg/ml聚-L-鸟氨酸预处理,然后离心,并将细胞直接重悬于相同混合物中,同时加入2至4μg/ml TMV。较高浓度的聚阳离子和缓冲液对原生质体有毒性。在最佳条件下,可获得约10-20μg TMV/10⁶原生质体的病毒产量,而在培养72小时后,通常可从培养液中回收大量病毒。接种后2小时向原生质体培养物中添加放线菌素D可部分抑制感染性的发展。