Robertson N L, French R
USDA, Agricultural Research Service, Subarctic Agricultural Research Unit, Arctic Germplasm Introduction and Research Project, University of Alaska-Fairbanks, Palmer Research Station, Palmer, AK 99645, USA.
Arch Virol. 2007 Feb;152(2):369-82. doi: 10.1007/s00705-006-0846-4. Epub 2006 Oct 2.
A new plant virus belonging to the family Luteoviridae and isolated from diseased oat (Avena sativa L.) plants was discovered in Alaska in 2003. Even though plants with red/orange leaves were indicative of barley yellow dwarf disease, they were not reactive to specific antibodies corresponding to barley yellow dwarf virus (BYDV)-MAV, -PAV, -SGV, and cereal yellow dwarf virus-RPV from enzyme-linked immunosorbent assays (ELISA). An alternative RT-PCR assay that incorporated Shu-F/Yan-R primers for detection of BYDV-MAV, -PAS, -PAV, and SGV was effective in producing approximately 830-nt fragments that contained genomic sequences to the 3'-terminus of the polymerase gene (ORF 2), the intergenic region ( approximately 113 nt), the coat protein gene (ORF 3), and the putative movement gene (ORF 4). The Alaskan isolates were most similar to BYDV-MAV with only about 77 and 80% amino acid identity in the CP and ORF 4, respectively. The Alaska isolates coat protein gene sequences differed in several regions that otherwise are conserved among BYDV-MAV isolates, and may be important in serological variations, accounting for the negative ELISA results. Based upon sequence and serological differences, we concluded that the Alaskan BYDV-MAV-like isolates formed a novel species tentatively in the genus Luteovirus, and propose the name BYDV-ORV (oat red-leaf virus).
2003年在阿拉斯加发现了一种属于黄症病毒科的新型植物病毒,它是从患病的燕麦( Avena sativa L.)植株中分离出来的。尽管叶片呈红色/橙色的植株表明感染了大麦黄矮病,但通过酶联免疫吸附测定(ELISA),它们与对应于大麦黄矮病毒(BYDV)-MAV、-PAV、-SGV以及禾谷类黄矮病毒-RPV的特异性抗体没有反应。一种采用Shu-F/Yan-R引物检测BYDV-MAV、-PAS、-PAV和SGV的替代逆转录聚合酶链反应(RT-PCR)检测方法,有效地产生了约830个核苷酸的片段,这些片段包含了聚合酶基因(开放阅读框2)3'端、基因间隔区(约113个核苷酸)、外壳蛋白基因(开放阅读框3)以及假定的移动基因(开放阅读框4)的基因组序列。阿拉斯加分离株与BYDV-MAV最为相似,在外壳蛋白(CP)和开放阅读框4中氨基酸同一性分别仅约为77%和80%。阿拉斯加分离株的外壳蛋白基因序列在几个区域存在差异,而这些区域在BYDV-MAV分离株中通常是保守的,可能在血清学变异中起重要作用,这解释了ELISA结果为阴性的原因。基于序列和血清学差异,我们得出结论,阿拉斯加的BYDV-MAV样分离株在黄症病毒属中初步形成了一个新种,并提议将其命名为BYDV-ORV(燕麦红叶病毒)。