McGeoch D J
Medical Research Council Virology Unit, Institute of Virology, University of Glasgow, Church Street, Glasgow G11 5JR, UK.
Philos Trans R Soc Lond B Biol Sci. 2001 Apr 29;356(1408):421-35. doi: 10.1098/rstb.2000.0775.
Genomic sequences available for members of the gamma-Herpesvirinae allow analysis of many aspects of the group's evolution. This paper examines four topics: (i) the phylogeny of the group; (ii) the histories of gamma-herpesvirus-specific genes; (iii) genomic variation of human herpesvirus 8 (HHV-8); and (iv) the relationship between Epstein-Barr virus types 1 and 2 (EBV-1 and EBV-2). A phylogenetic tree based on eight conserved genes has been constructed for eight gamma-herpesviruses and extended to 14 species with smaller gene sets. This gave a generally robust assignment of evolutionary relationships, with the exception of murine herpesvirus 4 (MHV-4), which could not be placed unambiguously on the tree and which has evidently experienced an unusually high rate of genomic change. The gamma-herpesviruses possess a variable complement of genes with cellular homologues. In the clearest cases these virus genes were shown to have originated from host genome lineages in the distant past. HHV-8 possesses at its left genomic terminus a highly diverse gene (K1) and at its right terminus a gene (K15) having two diverged alleles. It was proposed that the high diversity of K1 results from a positive selection on K1 and a hitchhiking effect that reduces diversity elsewhere in the genome. EBV-1 and EBV-2 differ in their alleles of the EBNA-2, EBNA-3A, EBNA-3B and EBNA-3C genes. It was suggested that EBV-1 and EBV-2 may recombine in mixed infections so that their sequences outside these genes remain homogeneous. Models for genesis of the types, by recombination between diverged parents or by local divergence from a single lineage, both present difficulties.
γ-疱疹病毒亚科成员的基因组序列有助于分析该类病毒进化的诸多方面。本文探讨了四个主题:(i)该类病毒的系统发育;(ii)γ-疱疹病毒特异性基因的历史;(iii)人类疱疹病毒8型(HHV-8)的基因组变异;以及(iv)爱泼斯坦-巴尔病毒1型和2型(EBV-1和EBV-2)之间的关系。基于八个保守基因构建了八株γ-疱疹病毒的系统发育树,并扩展到基因集较小的14个物种。这给出了一个总体上可靠的进化关系归属,但鼠疱疹病毒4型(MHV-4)除外,它无法明确地置于该树上,且显然经历了异常高的基因组变化率。γ-疱疹病毒拥有与细胞同源物可变的基因互补。在最明显的情况下,这些病毒基因被证明起源于遥远过去的宿主基因组谱系。HHV-8在其基因组左末端有一个高度多样化的基因(K1),在其右末端有一个具有两个分歧等位基因的基因(K15)。有人提出,K1的高度多样性是由对K1的正选择以及降低基因组其他部位多样性的搭便车效应导致的。EBV-1和EBV-2在EBNA-2、EBNA-3A、EBNA-3B和EBNA-3C基因的等位基因上存在差异。有人认为,EBV-1和EBV-2可能在混合感染中发生重组,从而使这些基因之外的序列保持一致。通过分化亲本之间的重组或从单一谱系的局部分化来产生这些类型的模型都存在困难。