Frisque R J
Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park 16802, USA.
Dev Biol Stand. 1998;94:103-13.
Recombination between different primate polyomavirus genomes (SV40, JCV, BKV) or within the genome of the same species (e.g. archetype to rearranged type virus) might contribute to the establishment of SV40-like viruses within the human population. Alternatively, it is possible that these polyomaviruses might, upon co-infection of human cells, complement each other's growth through direct virus-virus interactions or by indirect effects on host cell permissiveness. Our laboratory has investigated the activity of JCV-BKV-SV40 chimaeras constructed in vitro, and some of them exhibit altered lytic, host range, and oncogenic behaviour. Our work has also included the PCR analysis of human tissue specimens for the presence of polyomaviral sequences. Archetype and rearranged variants of JC virus have been detected in normal and diseased tissues, but evidence for naturally arising JCV-BKV or JCV-SV40 recombinant genomes has not been obtained.
不同灵长类多瘤病毒基因组(SV40、JCV、BKV)之间或同一物种基因组内(例如原型病毒到重排型病毒)的重组可能有助于在人群中建立类似SV40的病毒。另外,这些多瘤病毒在共同感染人类细胞时,有可能通过病毒-病毒直接相互作用或对宿主细胞易感性的间接影响来相互补充生长。我们实验室研究了体外构建的JCV-BKV-SV40嵌合体的活性,其中一些表现出改变的裂解、宿主范围和致癌行为。我们的工作还包括对人类组织标本进行PCR分析,以检测多瘤病毒序列的存在。在正常和患病组织中已检测到JC病毒的原型和重排变体,但尚未获得自然产生的JCV-BKV或JCV-SV40重组基因组的证据。