Venktesh A, Watt F, Xu Z Z, Both G W
Molecular Science, CSIRO, North Ryde, NSW, Australia.
J Gen Virol. 1998 Mar;79 ( Pt 3):509-16. doi: 10.1099/0022-1317-79-3-509.
Ovine adenovirus OAV287 (OAV) is the prototype of a virus group which is phylogenetically distinct from the mastadenoviruses and aviadenoviruses. The genome arrangement of OAV showed that virus-associated (VA) RNA genes were not located between the reading frames for p52/55K and terminal protein as these overlapped. To determine whether VA genes were located elsewhere, several approaches were used. Nuclear extracts containing RNA polymerase III activity were used to transcribe OAV genome fragments in vitro. A product of approximately 120 bp was produced from two widely separated coding regions of the genome. However, when these were subcloned and used as radiolabelled probes to analyse RNA from OAV-infected cells, no VA-like RNA was detected, although late mRNAs that were transcribed from the regions were identified. In addition, 5' radiolabelling of small RNA species in control- and OAV-infected cells followed by gel analysis did not identify candidate VA RNAs. Radiolabelling of proteins in control- and OAV-infected cells showed that there was little preferential translation of viral proteins compared with host polypeptides, in contrast to the situation for adenovirus 5 (Ad5). In addition, the kinetics of OAV infection were slower than observed for human adenoviruses. Collectively, the data suggest that OAV is unique in that it does not produce VA RNA during infection. This conclusion is supported by a comparison of the genomes of the phylogenetically related OAV and egg drop syndrome viruses which shows that the VA gene identified in the latter is located in a region absent from OAV.
绵羊腺病毒OAV287(OAV)是一个病毒组的原型,该病毒组在系统发育上与哺乳动物腺病毒和禽腺病毒不同。OAV的基因组排列显示,病毒相关(VA)RNA基因并不位于p52/55K阅读框和末端蛋白之间,因为它们相互重叠。为了确定VA基因是否位于其他位置,采用了几种方法。利用含有RNA聚合酶III活性的核提取物在体外转录OAV基因组片段。从基因组的两个相距很远的编码区域产生了一个约120 bp的产物。然而,当将这些片段亚克隆并用作放射性标记探针来分析OAV感染细胞的RNA时,未检测到VA样RNA,尽管从这些区域转录的晚期mRNA被鉴定出来。此外,对对照细胞和OAV感染细胞中的小RNA物种进行5'放射性标记,随后进行凝胶分析,未鉴定出候选VA RNA。对对照细胞和OAV感染细胞中的蛋白质进行放射性标记显示,与腺病毒5(Ad5)的情况相反,与宿主多肽相比,病毒蛋白几乎没有优先翻译。此外,OAV感染的动力学比人类腺病毒观察到的要慢。总体而言,数据表明OAV的独特之处在于它在感染过程中不产生VA RNA。系统发育相关的OAV和减蛋综合征病毒的基因组比较支持了这一结论,该比较表明在后者中鉴定出的VA基因位于OAV不存在的区域。