Klaassen V A, Mayhew D, Fisher D, Falk B W
Department of Plant Pathology, University of California, Davis 95616, USA.
Virology. 1996 Aug 1;222(1):169-75. doi: 10.1006/viro.1996.0407.
Full-length cloned cDNAs of lettuce infectious yellows closterovirus (LIYV) RNAs 1 and 2 were constructed and fused to the bacteriophage T3 RNA polymerase promoter. To assess RNA replication, Nicotiana benthamiana protoplasts were inoculated with LIYV virion RNAs and LIYV cDNA-derived in vitro transcripts. Analysis of protoplasts inoculated with LIYV virion RNAs or capped (m7GpppG) in vitro transcripts from LIYV RNA 1 and 2 cDNAs showed accumulation of LIYV genomic and putative subgenomic RNAs (sgRNAs), synthesis of LIYV coat protein, and formation of LIYV virions. Furthermore, protoplasts inoculated with only capped in vitro transcripts from LIYV RNA 1 cDNA showed accumulation of LIYV RNA 1 and its putative sgRNA, indicating that LIYV RNA 1 can replicate in the absence of LIYV RNA 2. Conversely, accumulation of LIYV RNA 2 was not detectable in protoplasts inoculated with only LIYV RNA 2 cDNA-derived capped in vitro transcripts. These data demonstrate that LIYV genomic RNAs are competent for replication in mesophyll protoplasts and that infectious in vitro transcripts can be derived from the cloned cDNAs of a closterovirus genome.
构建了莴苣传染性黄化线形病毒(LIYV)RNA 1和RNA 2的全长克隆cDNA,并将其与噬菌体T3 RNA聚合酶启动子融合。为了评估RNA复制情况,用LIYV病毒粒子RNA和LIYV cDNA衍生的体外转录本接种本氏烟草原生质体。对接种LIYV病毒粒子RNA或来自LIYV RNA 1和2 cDNA的加帽(m7GpppG)体外转录本的原生质体进行分析,结果显示LIYV基因组RNA和假定的亚基因组RNA(sgRNA)积累、LIYV外壳蛋白合成以及LIYV病毒粒子形成。此外,仅接种来自LIYV RNA 1 cDNA的加帽体外转录本的原生质体显示出LIYV RNA 1及其假定sgRNA的积累,这表明LIYV RNA 1在没有LIYV RNA 2的情况下也能复制。相反,在仅接种来自LIYV RNA 2 cDNA的加帽体外转录本的原生质体中未检测到LIYV RNA 2的积累。这些数据表明,LIYV基因组RNA能够在叶肉原生质体中复制,并且传染性体外转录本可以从线形病毒基因组的克隆cDNA中获得。