Peeters B P, Gruijthuijsen Y K, de Leeuw O S, Gielkens A L
Institute for Animal Science and Health ID-Lelystad, The Netherlands.
Arch Virol. 2000;145(9):1829-45. doi: 10.1007/s007050070059.
We examined replication of Newcastle disease virus (NDV) by using minigenomes consisting of the 3' leader and 5' trailer regions of NDV flanking a reporter gene encoding secreted placental alkaline phosphatase (SEAP). Negative-sense minigenome RNA was generated from transfected plasmid DNA by means of in vivo transcription. Subsequent replication of minigenome RNA was determined either after infection with NDV helpervirus or after contransfection with helperplasmids that expressed the essential viral replication proteins NP, P, and L. In both systems, efficient replication of minigenome RNA was observed only if the genome size was a multiple of six nucleotides. Hence, in these systems, replication of NDV minigenome RNA's is strictly dependent on the rule-of-six. When the supernatant from helpervirus-infected, transfected cells was used to infect fresh monolayers, efficient transfer of SEAP activity by virus-like particles was observed only if the size of the minigenome RNA obeyed the rule-of-six. However, after several serial passages, we also observed efficient transfer of SEAP activity by virus-like particles derived from minigenome RNA's that did not obey the rule-of-six. Evidence was obtained which indicated that successful replication of these minigenomes was not due to a change in genome size.
我们通过使用由新城疫病毒(NDV)的3'前导区和5'尾区侧翼的报告基因组成的微型基因组来研究新城疫病毒(NDV)的复制,该报告基因编码分泌型胎盘碱性磷酸酶(SEAP)。通过体内转录从转染的质粒DNA产生负链微型基因组RNA。微型基因组RNA的后续复制在感染NDV辅助病毒后或与表达必需病毒复制蛋白NP、P和L的辅助质粒共转染后进行测定。在这两种系统中,只有当基因组大小是六个核苷酸的倍数时,才观察到微型基因组RNA的有效复制。因此,在这些系统中,NDV微型基因组RNA的复制严格依赖于六规则。当来自辅助病毒感染的转染细胞的上清液用于感染新鲜单层细胞时,只有当微型基因组RNA的大小遵循六规则时,才能观察到病毒样颗粒对SEAP活性的有效转移。然而,经过几次连续传代后,我们也观察到来自不遵循六规则的微型基因组RNA的病毒样颗粒对SEAP活性的有效转移。获得的证据表明,这些微型基因组的成功复制不是由于基因组大小的改变。