Caporale Marco, Cousens Christina, Centorame Patrizia, Pinoni Chiara, De las Heras Marcelo, Palmarini Massimo
Institute of Comparative Medicine, University of Glasgow Veterinary School, 464 Bearsden Road, Glasgow G61 1QH, Scotland.
J Virol. 2006 Aug;80(16):8030-7. doi: 10.1128/JVI.00474-06.
Jaagsiekte sheep retrovirus (JSRV) is the causative agent of ovine pulmonary adenocarcinoma (OPA). The expression of the JSRV envelope (Env) alone is sufficient to transform a variety of cell lines in vitro and induce lung cancer in immunodeficient mice. In order to determine the role of the JSRV Env in OPA tumorigenesis in sheep, we derived a JSRV replication-defective virus (JS-RD) which expresses env under the control of its own long terminal repeat (LTR). JS-RD was produced by transiently transfecting 293T cells with a two plasmid system, involving (i) a packaging plasmid, with the putative JSRV packaging signal deleted, expressing the structural and enzymatic proteins Gag, Pro, and Pol, and (ii) a plasmid which expresses env in trans for JS-RD particles and provides the genomes necessary to deliver JSRV env upon infection. During the optimization of the JS-RD system we determined that both R-U5 (in the viral 5' LTR) and the env region are important for JSRV particle production. Two independent experimental transmission studies were carried out with newborn lambs. Four of five lambs inoculated with JS-RD showed OPA lesions in the lungs at various times between 4 and 12 months postinoculation. Abundant expression of JSRV Env was detected in tumor cells of JS-RD-infected animals and PCR assays confirmed the presence of the deleted JS-RD genome. These data strongly suggest that the JSRV Env functions as a dominant oncoprotein in the natural immunocompetent host and that JSRV can induce OPA in the absence of viral spread.
绵羊肺腺瘤逆转录病毒(JSRV)是绵羊肺腺癌(OPA)的病原体。单独JSRV包膜(Env)的表达就足以在体外转化多种细胞系,并在免疫缺陷小鼠中诱发肺癌。为了确定JSRV Env在绵羊OPA肿瘤发生中的作用,我们构建了一种JSRV复制缺陷型病毒(JS-RD),其在自身长末端重复序列(LTR)的控制下表达env。通过用双质粒系统瞬时转染293T细胞来产生JS-RD,该系统包括:(i)一个包装质粒,其假定的JSRV包装信号被删除,表达结构和酶蛋白Gag、Pro和Pol;(ii)一个质粒,其为JS-RD颗粒反式表达env,并提供感染时传递JSRV env所需的基因组。在优化JS-RD系统的过程中,我们确定R-U5(在病毒5' LTR中)和env区域对JSRV颗粒的产生都很重要。对新生羔羊进行了两项独立的实验性传播研究。接种JS-RD的五只羔羊中有四只在接种后4至12个月的不同时间出现了肺部OPA病变。在JS-RD感染动物的肿瘤细胞中检测到JSRV Env的大量表达,PCR检测证实了缺失的JS-RD基因组的存在。这些数据有力地表明,JSRV Env在天然免疫健全宿主中作为一种显性癌蛋白发挥作用,并且JSRV在没有病毒传播的情况下也能诱发OPA。