Abdalla O A, Ali A
Department of Biological Science, The University of Tulsa, OK 74104.
Plant Dis. 2012 Nov;96(11):1705. doi: 10.1094/PDIS-07-12-0630-PDN.
Alfalfa mosaic virus (AMV), a member of the genus Alfamovirus, family Bromoviridae (1), has been reported in 44 states in the United States excluding Oklahoma. During a cucurbit survey in the summer of 2010, severe mosaic and mottling symptoms were observed on many peppers (Capsicum annuum) and white clover (Trifolium repens) plants in Tulsa, Oklahoma. Symptomatic leaf samples from 15 pepper and two white clover plants were collected in the Bixby area and analyzed serologically by dot-immunobinding assay (DIBA) using specific polyclonal antibodies against AMV (Agdia, Inc). Seven out of 15 pepper samples and both white clover samples were tested positive by DIBA to AMV. The remaining symptomatic samples were positive to Cucumber mosaic virus (CMV). Total RNA was extracted from DIBA positive AMV samples by Tri-reagent method. A small aliquot of total RNA was tested by reverse transcription (RT)-PCR using specific primers: AMV-F 5' GTCCGCGATCTCTTAAAT 3' and AMV-R 5' GAAGTTTGGGTCGAGAGA 3' that were designed to amplify 900 bp of the AMV-RNA 3. Analysis of the PCR products on agarose gel electrophoreses showed that all tested samples showed a band of the expected size while DIBA negative AMV samples did not produce any band. The amplified PCR product (900 bp) obtained from pepper and white clover were cleaned with PCR purification kit (Qiagen, Germantown, MD) and directly sequenced bi-directionally using the above primers. Sequence analysis confirmed that this virus shared 97% identity at nucleotide sequence with RNA 3 of AMV isolate from Madison-USA (GenBank Accession No. K02703). For biological and morphological characterization of the virus, eight pepper plants were mechanically inoculated using 0.1 M KHPO buffer (pH 7.2) with total RNA extracted from AMV positive pepper or white clover plant samples. One to two weeks post-inoculation, all inoculated plants produced severe mosaic, mottling, and stunting. Virus-like particles preparations were obtained from these symptomatic plants according to our previously described method (2) and electron microcopy examination showed typical AMV particles. These biological and morphological data further confirmed the presence of AMV infecting pepper and clover in Oklahoma. AMV is a significant pathogen worldwide and infects more than 600 species in 70 families, especially alfalfa, pepper, soybean, and tobacco (3). AMV has a worldwide distribution, including the United States, and particularly the Midwestern U.S. where the incidence of the virus is on the rise recently because of the presence of its vector (Aphis glycines) (4). To our knowledge, this is the first report of AMV infecting crops in Oklahoma, which could pose a threat to other economic crops grown in Oklahoma, especially soybean. References: (1) E. E. Mueller et al. Plant Dis. 91:266, 2007. (2) A. Ali et al. Plant Dis. 96:243, 2012. (3) J. F. Bol. Mol. Plant Path.4:1, 2003. (4) M. Malapi-Nelson et al. Plant Dis.93:1259, 2009.
苜蓿花叶病毒(AMV)是雀麦花叶病毒科苜蓿花叶病毒属的成员(1),在美国除俄克拉何马州外的44个州均有报道。在2010年夏季的一次葫芦科植物调查中,俄克拉何马州塔尔萨市的许多辣椒(辣椒属)和白三叶草(白车轴草)植株上观察到严重的花叶和斑驳症状。从比克斯比地区15株辣椒和2株白三叶草的有症状叶片样本中采集样本,并使用针对AMV的特异性多克隆抗体(Agdia公司)通过斑点免疫结合试验(DIBA)进行血清学分析。15份辣椒样本中的7份以及两份白三叶草样本通过DIBA检测对AMV呈阳性。其余有症状样本对黄瓜花叶病毒(CMV)呈阳性。通过Tri-reagent法从DIBA阳性的AMV样本中提取总RNA。使用特异性引物:AMV-F 5' GTCCGCGATCTCTTAAAT 3'和AMV-R 5' GAAGTTTGGGTCGAGAGA 3'通过逆转录(RT)-PCR对一小部分总RNA进行检测,这些引物设计用于扩增AMV-RNA 3的900 bp片段。在琼脂糖凝胶电泳上对PCR产物进行分析表明,所有检测样本均显示出预期大小的条带,而DIBA阴性的AMV样本未产生任何条带。从辣椒和白三叶草中获得的扩增PCR产物(900 bp)用PCR纯化试剂盒(Qiagen公司,马里兰州杰曼敦)进行纯化,并使用上述引物直接进行双向测序。序列分析证实,该病毒在核苷酸序列上与来自美国麦迪逊的AMV分离株的RNA 3具有97%的同一性(GenBank登录号:K02703)。为了对该病毒进行生物学和形态学特征分析,使用0.1 M KHPO缓冲液(pH 7.2)和从AMV阳性辣椒或白三叶草植株样本中提取的总RNA对8株辣椒植株进行机械接种。接种后1至2周,所有接种植株均出现严重的花叶、斑驳和矮化症状。根据我们之前描述的方法(2)从这些有症状的植株中获得病毒样颗粒制剂,电子显微镜检查显示典型的AMV颗粒。这些生物学和形态学数据进一步证实了俄克拉何马州存在感染辣椒和三叶草的AMV。AMV是一种在全球范围内重要的病原体,可感染70个科的600多种植物,尤其是苜蓿、辣椒、大豆和烟草(3)。AMV在全球范围内分布,包括美国,特别是美国中西部地区,由于其传播媒介(大豆蚜)的存在,该病毒的发病率最近有所上升(4)。据我们所知,这是AMV感染俄克拉何马州作物的首次报道,这可能对俄克拉何马州种植的其他经济作物,尤其是大豆构成威胁。参考文献:(1)E. E. Mueller等人,《植物病害》91:266,2007年。(2)A. Ali等人,《植物病害》96:243,2012年。(3)J. F. Bol,《分子植物病理学》4:1,2003年。(4)M. Malapi-Nelson等人,《植物病害》93:1259,2009年。