Kikhno Iryna, Gutiérrez Serafín, Croizier Liliane, Croizier Guy, Ferber Miguel López
Laboratoire de Pathologie Comparée, UMR 5087 INRA/CNRS/Université de Montpellier II, 30380 Saint Christol les Alès, France1.
J Gen Virol. 2002 Dec;83(Pt 12):3013-3022. doi: 10.1099/0022-1317-83-12-3013.
During plaque purification of Spodoptera littoralis nucleopolyhedrovirus in S. littoralis Sl52 cell culture, a deletion mutant virus was isolated. Analysis of the biological properties of this mutant virus revealed an absence of per os infectivity of the occluded virus. Infectivity by injection of the non-occluded (budded) virus is not different between the wild-type and the deleted virus. Restriction analysis of the mutant virus genome revealed a 4.5 kb deletion within the NotI D fragment. The observed phenotype was mapped to the deleted region by rescue experiments. The deletion was characterized and the equivalent DNA fragment on the wild-type virus was sequenced. By co-transfecting the DNA of the deleted virus with plasmids derived from the wild-type virus, it was possible to determine that ORF 7 in this fragment is responsible for the observed phenotype. ORF 7, called pif (per os infectivity factor), is homologous to ORF 119 of Autographa californica nucleopolyhedrovirus. Similar ORFs are present in all sequenced baculoviruses. The product of this gene is an occlusion body-derived virion structural protein required only for the first steps of larva infection, as viruses being produced in cells expressing the gene but not containing it in their genomes are able to produce successful infections.
在斜纹夜蛾核型多角体病毒于斜纹夜蛾Sl52细胞培养物中进行噬菌斑纯化期间,分离出一种缺失突变病毒。对该突变病毒生物学特性的分析显示,被包埋病毒缺乏经口感染性。野生型病毒和缺失病毒通过注射非包埋(出芽型)病毒的感染性并无差异。对突变病毒基因组的限制性分析显示,在NotI D片段内有一个4.5 kb的缺失。通过拯救实验将观察到的表型定位到缺失区域。对该缺失进行了表征,并对野生型病毒上的等效DNA片段进行了测序。通过将缺失病毒的DNA与源自野生型病毒的质粒共转染,得以确定该片段中的开放阅读框7(ORF 7)是导致观察到的表型的原因。ORF 7被称为经口感染性因子(pif),与苜蓿银纹夜蛾核型多角体病毒的ORF 119同源。所有已测序的杆状病毒中都存在类似的开放阅读框。该基因的产物是一种源自包涵体的病毒粒子结构蛋白,仅在幼虫感染的最初阶段是必需的,因为在表达该基因但基因组中不包含该基因的细胞中产生的病毒能够成功感染。