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Molecular characterization of a cucumber mosaic cucumovirus isolated from lettuce in Egypt

机译:埃及莴苣中分离的黄瓜花叶黄瓜花叶病毒的分子特征

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Abstract Cucumber mosaic cucumovirus (CMV) was isolated from lettuce plants (Lactuca saliva) showing virus like symptoms. Isolation was performed depending on specific polyclonal antibodies and Chenopodium quinoa as a local lesion host. Virus was purified from 200 gm of virus-infected Nicotiana tabacum cv. White Burley leaves giving /426o/28o ratio of 1.21 and a yield of 1.7 mg. Purified virus preparation was used for rabbit immunization to produce specific polyclonal antibodies. IgGs were purified and evaluated by indirect enzyme linked immunosorbant assay (I-ELISA) to determine the dilution end point which found to be 1:512. Electron micrographs showed spherical virus particles of about 30 nm in diameter. Virus coat protein (CP) molecular weight was determined using sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), giving a single band of 25 kDa within resolving gel. Immunocapture-reverse transcriptase-polymerase chain reaction (IC-RT-PCR) was used for the amplification of CMVcoat protein gene (cp), the appearance of 657 bp bands confirmed the expected size of such gene. Comparing virus cp gene sequence with the sequences of seven overseas isolates confirmed that the under study isolate was related to the CMV subgroup I.
机译:摘要从表现出病毒样症状的莴苣植物(唾液乳杆菌)中分离出黄瓜花叶黄瓜花叶病毒(CMV)。根据特定的多克隆抗体和藜藜藜作为局部病变宿主进行分离。从200克病毒感染的烟草(Nicotiana tabacum)cv中纯化病毒。白白肋烟叶的/ 426o / 28o比为1.21,产量为1.7 mg。纯化的病毒制剂用于兔免疫,以产生特异的多克隆抗体。纯化IgG,并通过间接酶联免疫吸附测定(I-ELISA)进行评估,以确定稀释终点为1:512。电子显微照片显示直径约30 nm的球形病毒颗粒。使用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)测定病毒外壳蛋白(CP)的分子量,在分离凝胶中给出25 kDa的单条带。免疫捕获逆转录酶-聚合酶链反应(IC-RT-PCR)被用于CMVcoat蛋白基因(cp)的扩增,657 bp条带的出现证实了该基因的预期大小。将病毒cp基因序列与7个海外分离株的序列进行比较,证实了正在研究的分离株与CMV I组有关。

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