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海南黄灯笼辣椒顶死病病原病毒的分离鉴定
引用本文:王健华,刘志昕,王运勤,吉训聪,肖敏,郑服丛.海南黄灯笼辣椒顶死病病原病毒的分离鉴定[J].热带作物学报,2005,26(3):96-102.
作者姓名:王健华  刘志昕  王运勤  吉训聪  肖敏  郑服丛
作者单位:1. 中国热带农业科学院热带生物技术研究所,热带作物生物技术国家重点实验室,海口,571101;华南热带农业大学植物保护学院,海南,儋州,571737
2. 中国热带农业科学院热带生物技术研究所,热带作物生物技术国家重点实验室,海口,571101
3. 海南省农业科学院植保所,海口,571100
4. 华南热带农业大学植物保护学院,海南,儋州,571737
基金项目:海南省2003年科学事业费项目,华南热带农业大学2003年校基金项目.
摘    要:从海南省黄灯笼辣椒顶死病株上分离纯化得到一个病毒分离物.研究结果表明,该病毒分离物能通过汁液磨擦接种侵染供试植物中的4科11种植物,可由桃蚜传播;提纯病毒粒子呈球形,直径28~30 nm,外壳蛋白分子量约为28 ku;分离物与CMV抗血清在ELISA测定中呈阳性反应;提取病毒分离物RNA,应用RT-PCR方法克隆了病毒外壳蛋白(CP)基因.CP基因675 bp,编码218个氨基酸.对CP基因序列分析表明,该病毒分离物的CP基因核苷酸序列与黄瓜花叶病毒亚组Ⅰ分离物的同源性均在92.1%以上,所推导的氨基酸序列同源性在96.3%以上,而与亚组Ⅱ分离物的核苷酸序列同源性均低于77.3%,所推导的氨基酸序列同源性均低于80.7%.据此将该病毒分离物鉴定为黄瓜花叶病毒,归属于亚组Ⅰ.

关 键 词:黄灯笼辣椒  顶死  黄瓜花叶病毒  亚组Ⅰ  序列分析
收稿时间:2005-01-25
修稿时间:2005-01-252005-06-13

Etiological Identification of Tip Necrosis Disease in Capsicum chinense in Hainan
Wang Jianhua,Liu Zhixin,Wang Yunqin,Ji Xuncong,Xiao Min,Zheng Fucong.Etiological Identification of Tip Necrosis Disease in Capsicum chinense in Hainan[J].Chinese Journal of Tropical Crops,2005,26(3):96-102.
Authors:Wang Jianhua  Liu Zhixin  Wang Yunqin  Ji Xuncong  Xiao Min  Zheng Fucong
Institution:1 State Key Biotechnology Laboratory for Tropical Crops/Institute of Tropical Bioscience and Biotechnology, CATAS, Haikou 571101; 2 Hainan Academy of Agricultural Sciences, Haikou 571100; 3 Plant Protection College, SCUTA, Danzhou 571737
Abstract:An isolate of cucumber mosaic virus (CMV) was obtained from Capsicum ch inense leaves whose tip showed necrosis. The study of the host responses to viru s infection suggested that the isolate could infect plants of 11species from 4 f amilies, and was transmitted by Myzus persicae. Electron microscopy study reveal ed that the purified virus particle was spherical in shape and 28~30 nm in diame ter. The molecular weight of the coat protein (CP) subunit was about 28 ku based on SDS-PAGE. The isolate showed positive reaction when detected with the CMV an tiserum by ELISA. The CP gene was amplified by RT-PCR using the genomic RNA as t emplate and a pair of primers specific to CMV. Sequencing results showed that th e CP gene of the isolate had 675 bp encoding 218 amino acids. The nucleotide seq uences and amino acid sequences of the isolate shared over 92.1 % and 96.3 % hom ology with those of other isolates belonging to the subgroup I of CMV, respectiv ely, but less than 77.3 % and 80.7 % homology with those of other isolates belon ging to the subgroup II, respectively. In this context, the isolate was identifi ed as an isolate of CMV, belonging to the subgroup I.
Keywords:Capsicum chinense tip necrosis cucumber mosaic virus (CMV) subgroup I sequencing
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