Howley P M, Lafont B, Spehner D, Kaelin K, Billeter M A, Drillien R
Etablissement de Transfusion Sanguine de Strasbourg, CJF 94-03 INSERM, France.
J Virol Methods. 1999 Apr;79(1):65-74. doi: 10.1016/s0166-0934(99)00012-9.
Measles virus encodes three proteins required for the encapsidation, transcription and replication of viral genomes. The genes for these proteins have been inserted into the vaccinia virus genome together with the gene for the bacteriophage T7 RNA polymerase. Cells infected with this recombinant virus were able to encapsidate, transcribe and replicate a CAT gene positioned in the negative polarity behind a T7 promoter and flanked by measles virus genomic termini. Inhibition of the accumulation of the nucleocapsid proteins by actinomycin D led to an increase in CAT expression. Thus the measles virus polymerase activity, encoded by the vaccinia genome, was regulated by the level of measles proteins just as the authentic polymerase. The recombinant vaccinia described in this study could be useful for the production of measles virus-like particles encoding foreign genes and employed in vaccination or gene therapy strategies.
麻疹病毒编码病毒基因组衣壳化、转录和复制所需的三种蛋白质。这些蛋白质的基因已与噬菌体T7 RNA聚合酶的基因一起插入痘苗病毒基因组中。感染这种重组病毒的细胞能够将位于T7启动子后方且两侧为麻疹病毒基因组末端的负链CAT基因进行衣壳化、转录和复制。放线菌素D对核衣壳蛋白积累的抑制导致CAT表达增加。因此,由痘苗基因组编码的麻疹病毒聚合酶活性如同真正的聚合酶一样受到麻疹病毒蛋白水平的调节。本研究中描述的重组痘苗病毒可用于生产编码外源基因的麻疹病毒样颗粒,并应用于疫苗接种或基因治疗策略。