Weng Qingbei, Yang Kai, Xiao Wei, Yuan Meijin, Zhang Wenjun, Pang Yi
School of Life Sciences, Guizhou Normal University, Guiyang 550001, PR China.
State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou 510275, PR China.
J Gen Virol. 2009 Dec;90(Pt 12):2871-2876. doi: 10.1099/vir.0.013334-0. Epub 2009 Aug 12.
After serially undiluted passage of Spodoptera exigua multiple nucleopolyhedrovirus (SeMNPV), persistently infected Se301 cells were established. A cell strain, in which no polyhedra or viral particles were observed, was cloned and designated P8-Se301-C1. The P8-Se301-C1 cells are morphologically similar to but grow slower than Se301 cells and they can homologously interfere with SeMNPV. PCR analysis showed that SeMNPV ie-0 and polyhedrin genes were present but DNA polymerase and orf67 genes were absent in P8-Se301-C1, suggesting that the cells harbour incomplete SeMNPV genomes. Dot-blot analysis demonstrated that 0.32+/-0.16 ng SeMNPV DNA was present in 1.25 x 10(5) P8-Se301-C1 cells. A quantitative real-time PCR assay showed that there were 13.2+/-4.3 copies of the SeMNPV polyhedrin gene in each cell. Nested RT-PCR demonstrated the presence of SeMNPV polyhedrin transcripts in P8-Se301-C1 cells. The fact that P8-Se301-C1 cells carry low levels of partial viral genome but do not produce viral progeny suggests a latent-like viral infection in the cells.
在对甜菜夜蛾多粒包埋核型多角体病毒(SeMNPV)进行连续无稀释传代后,建立了持续感染的Se301细胞。克隆了一个未观察到多角体或病毒粒子的细胞株,并命名为P8-Se301-C1。P8-Se301-C1细胞在形态上与Se301细胞相似,但生长速度比Se301细胞慢,并且它们可以同源干扰SeMNPV。PCR分析表明,P8-Se301-C1中存在SeMNPV ie-0和多角体蛋白基因,但不存在DNA聚合酶和orf67基因,这表明这些细胞含有不完整的SeMNPV基因组。斑点杂交分析表明,在1.25×10(5)个P8-Se301-C1细胞中存在0.32±0.16 ng的SeMNPV DNA。定量实时PCR分析表明,每个细胞中存在13.2±4.3个SeMNPV多角体蛋白基因拷贝。巢式RT-PCR证明P8-Se301-C1细胞中存在SeMNPV多角体蛋白转录本。P8-Se301-C1细胞携带低水平的部分病毒基因组但不产生病毒后代这一事实表明细胞中存在类似潜伏的病毒感染。