Tavassoli M, Shahraeen N, Ghorbani S
Division of Microbiology, College of Science, Alzahra University, Tehran, Iran.
Pak J Biol Sci. 2008 Dec 1;11(23):2624-8. doi: 10.3923/pjbs.2008.2624.2628.
During 2006-2007 growing seasons, survey were carried to identify a virus disease causing mosaic of soybean in the field in Southern region (Khozestan Province) of Iran. To detect the viral infection, diseased leaf samples showing mild mosaic and leaf malformation were collected from soybean fields in Dezful, located in Khozestan Province. Infected samples were carried to the lab in a proper condition on ice packages. TPIA and DAS-ELISA serological tests were applied to identify the viral agent. To investigate the host-range, several indicator plants were mechanically inoculated under green-house condition. Seed transmission of CPMMV was examined using the seeds obtained from infected plants. The virus isolate was not found to be seed-borne in Clark variety of soybean. Different steps of ultracentrifugation including sucrose density gradient (10-40%) were carried out in order to obtain partial purified virus. On the basis of biological, serological and EM results, CPMMV-Carla virus was identified in the infected soybean samples. This is the first report of CPMMV infection of soybean in Iran.
在2006 - 2007年生长季期间,开展了调查以鉴定伊朗南部地区(胡齐斯坦省)田间导致大豆花叶病的一种病毒病。为检测病毒感染情况,从位于胡齐斯坦省的迪兹富尔的大豆田采集了表现出轻度花叶和叶片畸形的患病叶片样本。将感染样本用冰袋妥善包装后送往实验室。应用TPIA和双抗夹心酶联免疫吸附测定血清学检测来鉴定病毒病原体。为研究寄主范围,在温室条件下对几种指示植物进行了机械接种。使用从受感染植株获得的种子检测了辣椒脉斑驳病毒(CPMMV)的种传情况。在大豆的克拉克品种中未发现该病毒分离物通过种子传播。进行了包括蔗糖密度梯度(10 - 40%)在内的不同步骤超速离心以获得部分纯化的病毒。基于生物学、血清学和电子显微镜结果,在受感染的大豆样本中鉴定出了辣椒脉斑驳病毒 - 卡拉病毒。这是伊朗大豆感染辣椒脉斑驳病毒的首次报道。