Presley J F, Polo J M, Johnston R E, Brown D T
Cell Research Institute, University of Texas, Austin 78712-7640.
J Virol. 1991 Apr;65(4):1905-9. doi: 10.1128/JVI.65.4.1905-1909.1991.
We have shown previously that processing of the Sindbis virus envelope protein precursor PE2 to envelope protein E2 is not required for virus maturation in cultured vertebrate fibroblast cells and that unprocessed PE2 can be incorporated into infectious virus in place of E2 (J. F. Presley and D. T. Brown, J. Virol. 63:1975-1980, 1989; D. L. Russell, J. M. Dalrymple, and R. E. Johnston, J. Virol. 63:1619-1629, 1989). To better understand the role of this processing event in the invertebrate vector portion of the alphavirus life cycle, we have examined the maturation of Sindbis virus mutants defective in PE2 processing in cultured mosquito cells. We found that although substantial amounts of structural proteins PE2, E1, and C were produced in infected mosquito (aedine) cell lines, very little infectious virus was released. When the period of infection was extended, plaque size variants appeared, some of which exhibited a restored ability to grow in mosquito cells. The nucleotide sequences of two such variants were determined. These variants contained point mutations that restored PE2 cleavage, indicating a genetic linkage between failure to cleave PE2 and failure to grow in mosquito cells.
我们之前已经表明,在培养的脊椎动物成纤维细胞中,辛德毕斯病毒包膜蛋白前体PE2加工成包膜蛋白E2对于病毒成熟并非必需,并且未加工的PE2可以代替E2掺入感染性病毒中(J.F.普雷斯利和D.T.布朗,《病毒学杂志》63:1975 - 1980,1989;D.L.拉塞尔、J.M.达尔林普尔和R.E.约翰斯顿,《病毒学杂志》63:1619 - 1629,1989)。为了更好地理解这一加工事件在甲病毒生命周期的无脊椎动物载体部分中的作用,我们研究了在培养的蚊细胞中PE2加工有缺陷的辛德毕斯病毒突变体的成熟情况。我们发现,尽管在感染的蚊(伊蚊属)细胞系中产生了大量的结构蛋白PE2、E1和C,但释放的感染性病毒却很少。当感染时间延长时,出现了噬斑大小变异体,其中一些表现出在蚊细胞中生长能力恢复。测定了两个这样的变异体的核苷酸序列。这些变异体包含恢复PE2切割的点突变,表明PE2切割失败与在蚊细胞中生长失败之间存在遗传联系。