Rebenstorf Kathrin, Candresse Thierry, Dulucq Marie Josée, Büttner Carmen, Obermeier Christian
Section Phytomedicine, Institute for Horticultural Sciences, Humboldt-Universität zu Berlin, Germany.
J Virol. 2006 Mar;80(5):2453-62. doi: 10.1128/JVI.80.5.2453-2462.2006.
Cherry leaf roll virus (CLRV) belongs to the Nepovirus genus within the family Comoviridae. It has a host range which includes a number of wild tree and shrub species. The serological and molecular diversity of CLRV was assessed using a collection of isolates and samples recovered from woody and herbaceous host plants from different geographical origins. Molecular diversity was assessed by sequencing a short (375-bp) region of the 3' noncoding region (NCR) of the genomic RNAs while serological diversity was assessed using a panel of seven monoclonal antibodies raised initially against a walnut isolate of CLRV. The genomic region analyzed was shown to exhibit a significant degree of molecular variability with an average pairwise divergence of 8.5% (nucleotide identity). Similarly, serological variability proved to be high, with no single monoclonal antibody being able to recognize all isolates analyzed. Serological and molecular phylogenetic reconstructions showed a strong correlation. Remarkably, the diversity of CLRV populations is to a large extent defined by the host plant from which the viral samples are originally obtained. There are relatively few reports of plant viruses for which the genetic diversity is structured by the host plant. In the case of CLRV, we hypothesize that this situation may reflect the exclusive mode of transmission in natural plant populations by pollen and by seeds. These modes of transmission are likely to impose barriers to host change by the virus, leading to rapid biological and genetic separation of CLRV variants coevolving with different plant host species.
樱桃叶卷病毒(CLRV)属于双分病毒科中的线虫传多面体病毒属。它的寄主范围包括多种野生树木和灌木物种。利用从不同地理来源的木本和草本寄主植物中分离得到的毒株和样本,对CLRV的血清学和分子多样性进行了评估。通过对基因组RNA的3'非编码区(NCR)的一个短片段(375bp)进行测序来评估分子多样性,而血清学多样性则使用一组最初针对CLRV核桃分离株产生的七种单克隆抗体进行评估。结果表明,所分析的基因组区域表现出显著程度的分子变异性,平均成对差异为8.5%(核苷酸同一性)。同样,血清学变异性也很高,没有一种单克隆抗体能够识别所有分析的分离株。血清学和分子系统发育重建显示出很强的相关性。值得注意的是,CLRV群体的多样性在很大程度上由最初获得病毒样本的寄主植物决定。由寄主植物构建遗传多样性的植物病毒报道相对较少。就CLRV而言,我们推测这种情况可能反映了其在天然植物群体中通过花粉和种子的独特传播方式。这些传播方式可能会给病毒造成寄主变化的障碍,导致与不同植物寄主物种共同进化的CLRV变体在生物学和遗传上迅速分离。