Argaud O, Croizier L, López-Ferber M, Croizier G
Unité de Génétique des Virus, Station de Recherches de Pathologie Comparée, INRA-URA CNRS 2209, Saint Christol-Lés Alès, France.
J Gen Virol. 1998 Apr;79 ( Pt 4):931-5. doi: 10.1099/0022-1317-79-4-931.
Autographa californica nucleopolyhedrovirus (AcMNPV) does not replicate in Bombyx mori cells (Bm5, BmN). We have shown previously that when a short DNA sequence within AcMNPV ORF95, which encodes the viral helicase P143, is replaced with the colinear region of B. mori nucleopolyhedrovirus (BmNPV), AcMNPV gains the ability to replicate in Bm5 cells. To determine the mutational events in the p143 gene required to allow AcMNPV replication in B. mori cells, AcMNPV recombinants produced in Sf9 cells were screened in vivo in B. mori larvae, which are more permissive to baculovirus infection than B. mori cell lines. Eight combinations of mutations were tested and characterization of viral DNA extracted from dead larvae showed that amino acid changes at position 564 and 577 are required to kill B. mori larvae.
苜蓿银纹夜蛾核型多角体病毒(AcMNPV)不能在家蚕细胞(Bm5、BmN)中复制。我们之前已经表明,当AcMNPV ORF95内编码病毒解旋酶P143的一段短DNA序列被家蚕核型多角体病毒(BmNPV)的共线区域取代时,AcMNPV获得了在Bm5细胞中复制的能力。为了确定使AcMNPV在家蚕细胞中复制所需的p143基因中的突变事件,在Sf9细胞中产生的AcMNPV重组体在更易受杆状病毒感染的家蚕幼虫体内进行筛选。测试了八种突变组合,从死亡幼虫中提取的病毒DNA的特征表明,564位和577位的氨基酸变化是杀死家蚕幼虫所必需的。