Catalucci Daniele, Sporeno Elisabetta, Cirillo Agostino, Ciliberto Gennaro, Nicosia Alfredo, Colloca Stefano
Istituto di Ricerche di Biologia Molecolare P. Angeletti, Via Pontina Km 30.600, 00040 Pomezia, Roma, Italy.
J Virol. 2005 May;79(10):6400-9. doi: 10.1128/JVI.79.10.6400-6409.2005.
Production of multiply deleted adenoviral (Ad) vectors with increased cloning capacity and reduced immunogenicity to adenovirus gene products requires the concomitant generation of efficient packaging cell lines. High expression levels of the complementing genes must be achieved in a coordinated fashion with viral replication. This is a particularly difficult task in light of the significant cytotoxicity displayed by adenoviral proteins. To this end, we developed a novel adenovirus-based amplicon with an Epstein-Barr virus origin of replication, Ad type 5 (Ad5) inverted terminal repeats, all Ad5 early region 2 (E2) genes, and the early region 4 (E4) open reading frame 6 (ORF6) under the control of a tetracycline-dependent promoter. The amplicon (pE2) was stably maintained in multiple copies in the nuclei of 293 cells stably expressing the Epstein-Barr virus nuclear antigen 1 (EBNA1) and allowed replication as a linear DNA upon induction of E2 and ORF6 gene expression. A stable cell line (2E2) was generated by introducing pE2 into 293EBNATet cells expressing the tetracycline-dependent transcriptional silencer and the reverse Tet transactivator (rtTA2). Upon induction with doxicycline, 2E2 cells produced higher levels of polymerase, precursor terminal protein (pTP), and DNA binding protein than noninduced 2E2 cells infected with first-generation Ad5 vector and supported efficient amplification of a multiply deleted Ad5 vector lacking E1, E2, E3, and E4 genes (Ad5DeltaE(1-4)). The high cloning capacity of Ad5DeltaE(1-4) (up to 12.6 kb) was exploited to construct a vector encoding the entire hepatitis C virus (HCV) polyprotein. Infection of HeLa cells by the resulting vector showed high levels of correctly processed HCV proteins.
生产具有更高克隆能力且对腺病毒基因产物免疫原性降低的多重缺失腺病毒(Ad)载体,需要同时构建高效的包装细胞系。互补基因的高表达水平必须与病毒复制以协调的方式实现。鉴于腺病毒蛋白表现出的显著细胞毒性,这是一项特别困难的任务。为此,我们开发了一种新型的基于腺病毒的扩增子,其具有爱泼斯坦 - 巴尔病毒复制起点、5型腺病毒(Ad5)反向末端重复序列、所有Ad5早期区域2(E2)基因以及在四环素依赖性启动子控制下的早期区域4(E4)开放阅读框6(ORF6)。该扩增子(pE2)在稳定表达爱泼斯坦 - 巴尔病毒核抗原1(EBNA1)的293细胞的细胞核中以多拷贝形式稳定维持,并在诱导E2和ORF6基因表达时作为线性DNA进行复制。通过将pE2引入表达四环素依赖性转录沉默子和反向Tet反式激活因子(rtTA2)的293EBNATet细胞中,产生了一个稳定的细胞系(2E2)。在用强力霉素诱导后,2E2细胞产生的聚合酶、前体末端蛋白(pTP)和DNA结合蛋白水平高于感染第一代Ad5载体的未诱导2E2细胞,并支持对缺乏E1、E'、E3和E4基因的多重缺失Ad5载体(Ad5DeltaE(1-4))进行高效扩增。利用Ad5DeltaE(1-4)的高克隆能力(高达12.6 kb)构建了一个编码整个丙型肝炎病毒(HCV)多聚蛋白的载体。所得载体感染HeLa细胞后显示出高水平的正确加工的HCV蛋白。