Shukla D D, Ward C W
CSIRO, Division of Biotechnology, Parkville Laboratory, Victoria, Australia.
Arch Virol. 1989;106(3-4):171-200. doi: 10.1007/BF01313952.
The identification and classification of potyviruses has been in a very unsatisfactory state due to the large size of the group, the apparent vast variation among the members and the lack satisfactory taxonomic parameters that will distinguish distinct viruses from strains. In the past, use of classical methods, such as host range and symptomatology, cross-protection, morphology of cytoplasmic inclusions and conventional serology, revealed a "continuum" implying that the "species" and "strain" concepts cannot be applied to potyviruses. In contrast nucleic acid and amino acid sequence data of coat proteins has clearly demonstrated that potyviruses can be divided into distinct members and strains. This sequence data in combination with information of the structure of the potyvirus particle has been used to develop simple techniques such as HPLC peptide profiling, serology (using polyclonal antibody probes obtained by cross-adsorption with core protein from trypsin treated particles) and cDNA hybridization. These findings, along with immunochemical analyses of overlapping synthetic peptides have established the molecular basis for potyvirus serology; explained many of the problems associated with the application of conventional serology; and provided a sound basis for the identification and classification of potyviruses. As a result, the virus/strain status of some potyviruses has been redefined, requiring a change in the potyvirus nomenclature. These new developments necessitate a re-evaluation of the earlier literature on symptomatology, cross-protection, cytoplasmic inclusion body morphology and serology.
由于马铃薯Y病毒组规模庞大、成员间存在明显的巨大差异,且缺乏能区分不同病毒与毒株的令人满意的分类学参数,马铃薯Y病毒的鉴定和分类一直处于非常不理想的状态。过去,使用经典方法,如寄主范围和症状学、交叉保护、细胞质内含体形态以及传统血清学,揭示了一种“连续体”,这意味着“种”和“株”的概念不适用于马铃薯Y病毒。相比之下,外壳蛋白的核酸和氨基酸序列数据清楚地表明,马铃薯Y病毒可分为不同的成员和毒株。这些序列数据与马铃薯Y病毒粒子结构信息相结合,已被用于开发简单技术,如高效液相色谱肽谱分析、血清学(使用通过用胰蛋白酶处理的粒子的核心蛋白交叉吸附获得的多克隆抗体探针)和cDNA杂交。这些发现,连同对重叠合成肽的免疫化学分析,为马铃薯Y病毒血清学奠定了分子基础;解释了许多与传统血清学应用相关的问题;并为马铃薯Y病毒的鉴定和分类提供了坚实的基础。结果,一些马铃薯Y病毒的病毒/毒株状态被重新定义,这需要改变马铃薯Y病毒的命名法。这些新进展需要重新评估早期关于症状学、交叉保护、细胞质包涵体形态和血清学的文献。