巴基斯坦Pothwar地区黄瓜花叶病毒(CMV)外壳蛋白(CP)基因的血清学和分子鉴定

Z. Asad, M. Ahsan, M. Ashfaq
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摘要

黄瓜花叶病毒(Cucumber mosaic virus, CMV)是一种重要的植物病毒,对多种寄主具有重大威胁。巨细胞病毒在巴基斯坦的流行对蔬菜生产,特别是葫芦,是令人震惊的。本研究旨在估计该臭名昭著病毒的流行、分布和外壳蛋白碱基鉴定。2015-16年期间,在巴基斯坦Pothwar地区(拉瓦尔品第、阿托克、杰勒姆、查克瓦尔和伊斯兰堡)的黄瓜田记录了巨细胞病毒的发病率。在调查期间,收集了150份样品,并通过DASELISA(双抗体夹心酶联免疫吸附试验)进行了检测。结果表明,巨细胞病毒在整个地区普遍存在。疾病发病率最高的城市是拉瓦尔品第(50%),其次是查克瓦尔(46%)、阿托克(43%)、伊斯兰堡(40%)和杰勒姆(36%)。以指示植物辣椒(Capsicum annuum)、黄瓜(Cucumis sativus cv)、苋菜(Chenopodium amaranticolor)、藜麦(C. quinoa)、烟草(Nicotiana tabacum)和曼陀罗(Datura stramonium)为研究对象,采用机械接种法测定病毒的感染性。机械接种后,植株出现褪绿、坏死、花叶、发育迟缓、斑点等现象。通过聚合酶链式反应(Polymerase Chain Reaction, PCR)扩增出包衣蛋白(CP)基因特异性正向(CMVF-45)和反向(CMVR-45)引物,扩增出500bp片段。
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Serological and Molecular Identification Based on Coat Protein (CP) Gene of Cucumber mosaic Virus (CMV) Infecting Cucumber (Cucumis sativus L) in Pothwar Region of Pakistan
Cucumber mosaic virus (CMV) is one of the most important plant viruses and a major threat to a wide range of hosts. Prevalence of CMV in Pakistan is alarming for vegetable production especially cucurbits. The present study was done to estimate the prevalence, distribution as well as coat protein base identification of this notorious virus. During 2015-16 incidence of CMV was recorded in cucumber field in the Pothwar region of Pakistan (Rawalpindi, Attock, Jhelum, Chakwal, and Islamabad). During survey 150 samples were collected and tested through DASELISA (Double Antibody Sandwiched Enzyme Linked Immunosorbent Assay). Results show that CMV prevails throughout the region. Maximum disease incidence was recorded in Rawalpindi (50%) followed by Chakwal (46%), Attock (43%), Islamabad (40%) and Jhelum (36%). Virus infectivity was assayed by indicator plants (Capsicum annuum, Cucumis sativus cv, Chenopodium amaranticolor, C. quinoa, Nicotiana tabacum, and Datura stramonium) through mechanical inoculation. Upon mechanical inoculation, plants show Chlorotic lesion, Necrotic lesion, Mosaic, Stunting, Spots. Coat protein (CP) gene-specific forward (CMVF-45) and reverse (CMVR-45) primer amplified 500bp fragments through Polymerase Chain Reaction (PCR).
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