Olszewski J, Miller L K
Department of Genetics, University of Georgia, Athens 30602, USA.
J Virol. 1997 Jul;71(7):5040-50. doi: 10.1128/JVI.71.7.5040-5050.1997.
The defect in a temperature-sensitive mutant of Autographa californica nuclear polyhedrosis virus, tsN1054, was mapped and characterized. At the nonpermissive temperature of 33 degrees C, this mutant fails to form plaques upon infection of Sf-21 cultured insect cells; infection is limited to a single cell, even though the infection proceeds through the very late phase. Marker rescue mapping and DNA sequencing identified the gene, ORF 54, which was altered by a single nucleotide substitution in tsN1054. Transcriptional analysis of the ORF 54 region identified multicistronic RNAs, from early to very late times of infection, that potentially encode the ORF 54 gene product. Polyclonal antiserum raised to a TrpE-VP1054 fusion protein recognized a 42-kDa late protein, VP1054, in infected-cell lysates. VP1054 was found to be a component of both budded virus and occlusion-derived virions. The level of VP1054 was dramatically reduced in tsN1054-infected Sf-21 cells propagated at 33 degrees C, and electron microscopic analysis of these cells showed that nucleocapsids failed to form in the nuclei of these infected cells. Instead, novel round, electron-dense bodies were found associated with the virogenic stroma in tsN1054-infected cells. Therefore, VP1054 is a virus structural protein required for nucleocapsid assembly.
对苜蓿银纹夜蛾核型多角体病毒(Autographa californica nuclear polyhedrosis virus)的温度敏感突变体tsN1054的缺陷进行了定位和表征。在33℃的非允许温度下,该突变体感染Sf-21培养的昆虫细胞后无法形成噬菌斑;尽管感染会持续到非常晚期阶段,但感染仅限于单个细胞。通过标记拯救定位和DNA测序确定了基因ORF 54,它在tsN1054中因单个核苷酸替换而发生改变。对ORF 54区域的转录分析确定了从感染早期到非常晚期的多顺反子RNA,它们可能编码ORF 54基因产物。针对TrpE-VP1054融合蛋白产生的多克隆抗血清在感染细胞裂解物中识别出一种42 kDa的晚期蛋白VP1054。发现VP1054是出芽病毒和包埋衍生病毒粒子的组成成分。在33℃下培养的tsN1054感染的Sf-21细胞中,VP1054的水平显著降低,对这些细胞的电子显微镜分析表明,这些感染细胞的细胞核中未能形成核衣壳。相反,在tsN1054感染的细胞中,发现与病毒发生基质相关的新型圆形电子致密体。因此,VP1054是核衣壳组装所需的病毒结构蛋白。