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樱桃病毒A:双链RNA的cDNA克隆、核苷酸序列分析及血清学研究揭示甜樱桃中的一种新型植物毛病毒

Cherry virus A: cDNA cloning of dsRNA, nucleotide sequence analysis and serology reveal a new plant capillovirus in sweet cherry.

作者信息

Jelkmann W

机构信息

Federal Biological Research Centre for Agriculture and Forestry, Institute for Plant Protection in Fruit Crops, Dossenheim, Federal Republic of Germany.

出版信息

J Gen Virol. 1995 Aug;76 ( Pt 8):2015-24. doi: 10.1099/0022-1317-76-8-2015.

Abstract

The nucleotide sequence (7383 nucleotides) of a newly identified member of the genus Capillovirus, cherry virus A (CVA), was obtained from cDNA clones. The cDNA was generated from dsRNA extracted from plant tissue infected with little cherry virus (LCV). Small amounts of LCV dsRNA served as template nucleic acid and enabled the construction of a library of which, unexpectedly, 7.5% of the recombinant plasmids were specific for CVA. The genome organization of CVA resembles that of apple stem grooving virus (ASGV), the type member of the genus Capillovirus and is composed of a 266 kDa polyprotein (ORF1), a 52 kDa ORF2 located within ORF1 and a poly(A) tail. The 266 kDa ORF1 contains all the elements of a replication-related protein and has high identity with 'Sindbis-like' viruses. The ORF encodes the coat protein (CP) in the C-terminal region. The 52 kDa ORF2 has high identities with the putative viral cell-to-cell movement proteins of capillo- and trichoviruses. The CP was identified in immunoblot analysis and estimated to have a molecular mass of 24 kDa. Antiserum was obtained by expression of antigens as fusion proteins in Escherichia coli. There is significant sequence identity between CVA CP and the corresponding proteins of other capillo- and trichoviruses. However, no serological cross-reaction was obtained in immunoblot analysis with ASGV, apple chlorotic leafspot trichovirus (ACLSV), apple stem pitting virus (ASPV) and cherry mottle leaf virus (CMLV) antisera. Flexuous filamentous CVA virions were identified in extracts of sweet cherry by immunosorbent electron microscopy (ISEM) and decorated with the antiserum to the fusion protein. CVA was identified in three cherry sources of different disease status by ISEM, immunoblot analysis and hybridization to dsRNA. CVA is not closely related to any of the currently described diseases in cherry but it has all the properties of a capillovirus. It is suggested that CVA should be classified as a new member of the genus capillovirus.

摘要

从cDNA克隆中获得了一种新鉴定的毛形病毒属成员——樱桃病毒A(CVA)的核苷酸序列(7383个核苷酸)。该cDNA由从小樱桃病毒(LCV)感染的植物组织中提取的双链RNA(dsRNA)生成。少量的LCV dsRNA用作模板核酸,从而构建了一个文库,出乎意料的是,该文库中7.5%的重组质粒对CVA具有特异性。CVA的基因组结构类似于苹果茎沟病毒(ASGV),即毛形病毒属的典型成员,由一个266 kDa的多聚蛋白(开放阅读框1,ORF1)、一个位于ORF1内的52 kDa的ORF2和一个聚腺苷酸尾组成。266 kDa的ORF1包含复制相关蛋白的所有元件,并且与“辛德比斯样”病毒具有高度同源性。该开放阅读框在C末端区域编码外壳蛋白(CP)。52 kDa的ORF2与毛形病毒属和苹果花叶病毒属假定的病毒细胞间运动蛋白具有高度同源性。通过免疫印迹分析鉴定出CP,估计其分子量为24 kDa。通过在大肠杆菌中表达抗原作为融合蛋白获得了抗血清。CVA CP与其他毛形病毒属和苹果花叶病毒属的相应蛋白之间存在显著的序列同源性。然而,在免疫印迹分析中,用ASGV、苹果褪绿叶斑病毒(ACLSV)、苹果茎痘病毒(ASPV)和樱桃斑驳叶病毒(CMLV)抗血清未获得血清学交叉反应。通过免疫吸附电子显微镜(ISEM)在甜樱桃提取物中鉴定出了柔性丝状CVA病毒粒子,并用针对融合蛋白的抗血清进行了标记。通过ISEM、免疫印迹分析和与dsRNA杂交,在三种不同病害状态的樱桃来源中鉴定出了CVA。CVA与目前所描述的樱桃中的任何病害都没有密切关系,但它具有毛形病毒的所有特性。建议将CVA归类为毛形病毒属的一个新成员。

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