Naeger L K, Salomé N, Pintel D J
Department of Molecular Microbiology and Immunology, School of Medicine, University of Missouri, Columbia 65212.
J Virol. 1993 Feb;67(2):1034-43. doi: 10.1128/JVI.67.2.1034-1043.1993.
Detailed analysis of five NS2 mutants of the autonomous parvovirus minute virus of mice (MVMp) has revealed the following. At low multiplicities of infection, NS2 mutants killed NB324K cells as well as wild-type (wt) MVM did and grew to high titers, while in contrast they grew poorly and did not readily kill murine A9 cells. Following CaPO4 transfection of murine fibroblasts, NS2 mutant infectious clones generated approximately 10-fold less monomer replicative-form DNA than wt and no detectable progeny single-stranded DNA. On nonmurine semipermissive NB324K cells, however, these mutant plasmid clones generated near wt levels of all replicative DNA forms. After infection of highly synchronized murine fibroblasts by NS2 mutant virus at inputs equivalent to those of the wt, mutant monomer replicative-form DNA was decreased 5- to 10-fold compared with that of the wt, and progeny single-stranded DNA accumulation was decreased to an even greater extent. Both total and cytoplasmic NS2 mutant RNA was decreased, but the amount of total viral mRNA generated, relative to accumulated viral DNA in the same experiments, was similar to that seen in wt infection. The accumulation of virus-generated proteins was also decreased in NS2 mutant infection; however, the magnitude of this decrease, compared with that of wt infections, was significantly greater than the concomitant decrease in mutant-generated levels of accumulated cytoplasmic RNA, and this effect was most dramatic for VP2. There was no such disparity between the relative accumulation of mutant-generated RNA and protein in cells permissive for the growth of these mutants. These results suggest that translation of MVM viral RNA is specifically reduced in NS2 mutant infection of restrictive cells. Because the affected viral proteins are required for the efficient production of viral replicative DNA forms, these results reveal a fundamental, although perhaps not the only, role for NS2 in parvovirus infection.
对自主型细小病毒小鼠微小病毒(MVMp)的五个NS2突变体进行的详细分析揭示了以下情况。在低感染复数下,NS2突变体与野生型(wt)MVM一样能杀死NB324K细胞,并能生长到高滴度,而相比之下,它们在鼠源A9细胞中生长不佳,且不易杀死该细胞。在用磷酸钙转染鼠源成纤维细胞后,NS2突变体感染性克隆产生的单体复制型DNA比野生型少约10倍,且未检测到子代单链DNA。然而,在非鼠源半允许性NB324K细胞上,这些突变体质粒克隆产生的所有复制型DNA水平接近野生型。在用相当于野生型的接种量的NS2突变体病毒感染高度同步化的鼠源成纤维细胞后,与野生型相比,突变体单体复制型DNA减少了5至10倍,子代单链DNA的积累减少得更为明显。NS2突变体的总RNA和细胞质RNA均减少,但在相同实验中,相对于积累的病毒DNA产生的总病毒mRNA量与野生型感染时相似。NS2突变体感染时病毒产生的蛋白质积累也减少;然而,与野生型感染相比,这种减少的幅度明显大于突变体产生的积累的细胞质RNA水平的相应降低,且这种效应在VP2上最为显著。在允许这些突变体生长的细胞中,突变体产生的RNA和蛋白质的相对积累之间没有这种差异。这些结果表明,在限制细胞的NS2突变体感染中,MVM病毒RNA的翻译被特异性降低。由于受影响的病毒蛋白是高效产生病毒复制型DNA形式所必需的,这些结果揭示了NS2在细小病毒感染中的一个基本作用,尽管可能不是唯一的作用。