Sokhandan Bashir N, Nematollahi S, Torabi E
Plant Protection Department, University of Tabriz, 29 Bahman Blvd., Tabriz 51664, Iran.
Acta Virol. 2008;52(4):237-42.
To monitor genetic variation between Cucumber mosaic virus (CMV) isolates of northwest Iran, samples of cucurbitaceous plants expressing symptoms similar to those caused by CMV were collected. The samples were first screened by ELISA to detect CMV and to determine its subgroup. All detected CMV isolates appeared to be subgroup I (S-I). When total RNA from the samples was subjected to RT-PCR with a pair of primers corresponding to the CMV coat protein (CP) flanking regions, the expected ~870 bp DNA fragment was amplified at 18 samples of 34 tested. MspI restriction analysis of 18 amplified products produced two DNA fragments with sizes about 530 and 330 bp corresponding to MspI profile of CMV S-I. The amplification products of four representative samples were cloned and nucleotide sequences of 1-5 clones from each isolate were determined. The clones from each isolate were over 99% identical and also the isolates themselves were only up to 2% divergent. These isolates clustered in subgroup IA clade on a consensus phylogenetic tree and formed a distinct subclade suggesting that the isolates have originated from a common source.
为监测伊朗西北部黄瓜花叶病毒(CMV)分离株之间的遗传变异,采集了表现出与CMV引起的症状相似的葫芦科植物样本。首先通过ELISA对样本进行筛选,以检测CMV并确定其亚组。所有检测到的CMV分离株似乎都属于亚组I(S-I)。当用一对对应于CMV外壳蛋白(CP)侧翼区域的引物对样本的总RNA进行RT-PCR时,在34个测试样本中的18个样本中扩增出了预期的约870 bp DNA片段。对18个扩增产物进行MspI酶切分析,产生了两个大小约为530和330 bp的DNA片段,对应于CMV S-I的MspI酶切图谱。对四个代表性样本的扩增产物进行克隆,并测定每个分离株1-5个克隆的核苷酸序列。每个分离株的克隆之间的同一性超过99%,并且分离株本身之间的差异也仅高达2%。这些分离株在一个共有系统发育树上聚集在亚组IA分支中,并形成一个独特的亚分支,表明这些分离株起源于一个共同的来源。