Department of Medical Entomology, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku-ku, Tokyo 162-8640, Japan.
J Virol. 2011 Jul;85(13):6185-96. doi: 10.1128/JVI.00040-11. Epub 2011 Apr 20.
Among members of the order Mononegavirales, RNA splicing events have been found only in the family Bornaviridae. Here, we report that a new rhabdovirus isolated from the mosquito Culex tritaeniorhynchus replicates in the nuclei of infected cells and requires RNA splicing for viral mRNA maturation. The virus, designated Culex tritaeniorhynchus rhabdovirus (CTRV), shares a similar genome organization with other rhabdoviruses, except for the presence of a putative intron in the coding region for the L protein. Molecular phylogenetic studies indicated that CTRV belongs to the family Rhabdoviridae, but it is yet to be assigned a genus. Electron microscopic analysis revealed that the CTRV virion is extremely elongated, unlike virions of rhabdoviruses, which are generally bullet shaped. Northern hybridization confirmed that a large transcript (approximately 6,500 nucleotides [nt]) from the CTRV L gene was present in the infected cells. Strand-specific reverse transcription-PCR (RT-PCR) analyses identified the intron-exon boundaries and the 76-nt intron sequence, which contains the typical motif for eukaryotic spliceosomal intron-splice donor/acceptor sites (GU-AG), a predicted branch point, and a polypyrimidine tract. In situ hybridization exhibited that viral RNAs are primarily localized in the nucleus of infected cells, indicating that CTRV replicates in the nucleus and is allowed to utilize the host's nuclear splicing machinery. This is the first report of RNA splicing among the members of the family Rhabdoviridae.
在单负股病毒目中的成员中,只有博纳病毒科发现有 RNA 剪接事件。在这里,我们报告一种从三带喙库蚊中分离出的新的弹状病毒,它在感染细胞的核内复制,并需要 RNA 剪接来成熟病毒 mRNA。该病毒被命名为三带喙库蚊弹状病毒(CTRV),与其他弹状病毒具有相似的基因组组织,除了 L 蛋白编码区存在一个假定的内含子。分子系统发育研究表明,CTRV 属于 Rhabdoviridae 科,但尚未被分配属。电子显微镜分析表明,CTRV 病毒粒子非常细长,与弹状病毒的病毒粒子不同,后者通常呈子弹状。 northern 杂交证实,感染细胞中存在来自 CTRV L 基因的大转录本(约 6500 个核苷酸 [nt])。链特异性反转录 PCR(RT-PCR)分析鉴定了内含子-外显子边界和 76-nt 内含子序列,其中包含典型的真核剪接体内含子剪接供体/受体位点(GU-AG)、预测的分支点和多嘧啶序列。原位杂交显示病毒 RNA 主要定位于感染细胞的核内,表明 CTRV 在核内复制,并允许利用宿主的核剪接机制。这是 Rhabdoviridae 科成员中首次报道 RNA 剪接。