Joo M, Banerjee S, Makino S
Department of Microbiology, University of Texas at Austin 78712-1095, USA.
J Virol. 1996 Sep;70(9):5769-76. doi: 10.1128/JVI.70.9.5769-5776.1996.
The positive-strand defective interfering (DI) RNA of the murine coronavirus mouse hepatitis virus (MHV), when introduced into MHV-infected cells, results in DI RNA replication and accumulation. We studied whether the introduction of negative-strand transcripts of MHV DI RNA would also result in replication. At a location downstream of the T7 promoter and upstream of the human hepatitis delta virus ribozyme domain, we inserted a complete cDNA clone of MHV DI RNA in reverse orientation; in vitro-synthesized RNA from this plasmid yielded a negative-strand RNA copy of the MHV DI RNA. When the negative-strand transcripts of the DI RNA were expressed in MHV-infected cells by a vaccinia virus T7 expression system, positive-strand DI RNAs accumulated in the plasmid-transfected cells. DI RNA replication depended on the expression of T7 polymerase and on the presence of the T7 promoter. Transfection of in vitro-synthesized negative-strand transcripts into MHV-infected cells and serial passage of virus samples from RNA-transfected cells also resulted in accumulation of the DI RNA. Positive-strand DI RNA transcripts were undetectable in sample preparations of the in vitro-synthesized negative-strand DI RNA transcripts, and DI RNA did not accumulate after cotransfection of a small amount of positive-strand DI RNA and truncated-replication-disabled negative-strand transcripts; clearly, the DI RNA replicated from the transfected negative-strand transcripts and not from minute amounts of positive-strand DI RNAs that might be envisioned as artifacts of T7 transcription. Sequence analysis of positive-strand DI RNAs in the cells transfected with negative-strand transcripts showed that DI RNAs maintained the DI-specific unique sequences introduced within the leader sequence. These data indicated that positive-strand DI RNA synthesis occurred from introduced negative-strand transcripts in the MHV-infected cells; this demonstration, using MHV, of DI RNA replication from transfected negative-strand DI RNA transcripts is the first such demonstration among all positive-stranded RNA viruses.
将鼠冠状病毒小鼠肝炎病毒(MHV)的正链缺陷干扰(DI)RNA导入MHV感染的细胞后,会导致DI RNA的复制和积累。我们研究了导入MHV DI RNA的负链转录本是否也会导致复制。在T7启动子下游和人丁型肝炎病毒核酶结构域上游的位置,我们反向插入了MHV DI RNA的完整cDNA克隆;从该质粒体外合成的RNA产生了MHV DI RNA的负链RNA拷贝。当通过痘苗病毒T7表达系统在MHV感染的细胞中表达DI RNA的负链转录本时,正链DI RNA在质粒转染的细胞中积累。DI RNA的复制依赖于T7聚合酶的表达和T7启动子的存在。将体外合成的负链转录本转染到MHV感染的细胞中,并对来自RNA转染细胞的病毒样本进行连续传代,也导致了DI RNA的积累。在体外合成的负链DI RNA转录本的样本制备中未检测到正链DI RNA转录本,并且在共转染少量正链DI RNA和截短的复制缺陷负链转录本后,DI RNA没有积累;显然,DI RNA是从转染的负链转录本复制而来,而不是从可能被视为T7转录假象的微量正链DI RNA复制而来。对用负链转录本转染的细胞中的正链DI RNA进行序列分析表明,DI RNA保留了在前导序列中引入的DI特异性独特序列。这些数据表明,在MHV感染的细胞中,正链DI RNA的合成是由导入的负链转录本产生的;利用MHV进行的这一从转染的负链DI RNA转录本复制DI RNA的证明,是所有正链RNA病毒中的首例此类证明。