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胜红蓟黄脉中国病毒侵染越南百日草的首次报道

First Report of Ageratum yellow vein China virus Infecting Zinnia elegans in Vietnam.

作者信息

Li Z-B, Qin B-X, Cai J-H

机构信息

Institute of Plant Protection, Guangxi Academy of Agricultural Sciences, Nanning 530007, China.

出版信息

Plant Dis. 2013 Mar;97(3):431. doi: 10.1094/PDIS-10-12-0943-PDN.

Abstract

Whitefly-transmitted geminiviruses belong to the Geminiviridae family, which includes a group of plant DNA viruses that occurs in tropical and subtropical regions worldwide and caused severe leaf curl diseases on many crops. In July 2011, symptoms of mild yellowing and curling of leaves were observed on Zinnia elegans in Hue City, Vietnam. To identify possible begomoviruses, two samples with typical symptoms (Z1 and Z2) were collected and total DNA was extracted using PlantGen DNA Kit (CoWin Biotech Co., China). Using begomovirus-specific degenerate primer pair AV494 and AC1048 to amply geminivirus capsid protein gene (3), a 586-bp DNA fragment was amplified from both collected samples. The PCR products from Z1 and Z2 were cloned and sequenced. The partial sequences from two isolates had 96.8% similarity to each other and most closely related to Ageratum yellow vein China virus (AYVCNV) (98% identity to GenBank Accession Nos. AM940137.1 and AJ849916.1). Using two degenerate primer pairs bego1 (5'-ACMGGCCYATGWAYMGGAAG-3')/bego6 (5'-ACNGGDAARACRATGTGGGC-3') and bego2 (5'-CTTDATRTTBTCRTCCATCC-3')/bego3 (5'-CCWGGATTGCANARSAMGAT-3') to amplify full-length viral genome from Z1 (1). The complete DNA-A sequence from Z1 were determined to be 2,741 nucleotides (JX911332), showed high levels of sequence identity (89% [JN809812] to 98% [AJ849916.1 and AJ558120]) with AYVCNV and shared 98% nucleotide sequence identity with AYVCNV-G68 (AJ849916.1) and AYVCNV-G13 (AJ558120). No DNA-B component nor DNA-β could be detected using primers described previously (4). Zinnia leaf curl virus, Ageratum enation virus, Tobacco leaf curl virus, and Alternanthera yellow vein virus have been reported to be associated with Zinnia leaf curl disease (2). To our knowledge, this is the first report of AYVCNV infecting Z. elegans. AYVCNV was first reported in A. conyzoides on Hainan Island, China, and could infect L. esculentum (Solanaceae), A. conyzoides (Asteraceae), or tobacco (Solanaceae). Our results further corroborate that AYVCNV can infect Asteraceae plants. Therefore, this virus may pose a serious threat to many plants. References: (1) L. Lin et al. Plant Prot. 37:44, 2011. (2) P. Naveen et al. J. Biotechnol. Bioinform. 2:6, 2012. (3) S. D. Wyatt et al. Phytopathology 86:1288, 1996. (4) X. P. Zhou et al. J. Gen. Virol. 84:237, 2003.

摘要

粉虱传播的双生病毒属于双生病毒科,该科包括一组植物DNA病毒,它们分布于全球热带和亚热带地区,会在许多作物上引发严重的卷叶病。2011年7月,在越南顺化市的百日草上观察到叶片轻度黄化和卷曲的症状。为鉴定可能的菜豆金色花叶病毒属病毒,采集了两份具有典型症状的样本(Z1和Z2),并使用PlantGen DNA试剂盒(中国CoWin生物技术公司)提取了总DNA。使用菜豆金色花叶病毒属特异性简并引物对AV494和AC1048扩增双生病毒衣壳蛋白基因(3),从两份采集样本中均扩增出一个586 bp的DNA片段。对Z1和Z2的PCR产物进行克隆和测序。两个分离株的部分序列彼此相似性为96.8%,与藿香黄脉中国病毒(AYVCNV)关系最为密切(与GenBank登录号AM940137.1和AJ849916.1的同一性为98%)。使用两对简并引物bego1(5'-ACMGGCCYATGWAYMGGAAG-3')/bego6(5'-ACNGGDAARACRATGTGGGC-3')和bego2(5'-CTTDATRTTBTCRTCCATCC-3')/bego3(5'-CCWGGATTGCANARSAMGAT-3')从Z1扩增病毒全基因组(1)。Z1的完整DNA-A序列测定为2741个核苷酸(JX911332),与AYVCNV具有较高的序列同一性(与JN809812的同一性为89%,与AJ849916.1和AJ558120的同一性为98%),并与AYVCNV-G68(AJ849916.1)和AYVCNV-G13(AJ558120)共享98%的核苷酸序列同一性。使用先前描述的引物(4)未检测到DNA-B组分和DNA-β。据报道,百日草卷叶病毒、藿香耳突病毒、烟草卷叶病毒和莲子草黄脉病毒与百日草卷叶病有关(2)。据我们所知,这是AYVCNV感染百日草的首次报道。AYVCNV首次在中国海南岛的胜红蓟上被报道,可感染番茄(茄科)、胜红蓟(菊科)或烟草(茄科)。我们的结果进一步证实AYVCNV可感染菊科植物。因此,这种病毒可能对许多植物构成严重威胁。参考文献:(1)L. Lin等人,《植物保护》37:44,2011年。(2)P. Naveen等人,《生物技术与生物信息学杂志》2:6,2012年。(3)S. D. Wyatt等人,《植物病理学》86:1288,1996年。(4)X. P. Zhou等人,《普通病毒学杂志》84:237,2003年。

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