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巴基斯坦棉花感染黄秋葵脉突叶卷曲病毒及相关的棉花叶卷曲木尔坦β卫星和棉花叶卷曲木尔坦α卫星的首次报道:棉花叶卷曲病复合体的一个新成员

First Report of Okra enation leaf curl virus and Associated Cotton leaf curl Multan betasatellite and Cotton leaf curl Multan alphasatellite Infecting Cotton in Pakistan: A New Member of the Cotton Leaf Curl Disease Complex.

作者信息

Hameed U, Zia-Ur-Rehman M, Herrmann H-W, Haider M S, Brown J K

机构信息

Institute of Agricultural Sciences, University of the Punjab, Quaid-i-Azam Campus, Lahore, Pakistan.

School of Plant Sciences, The University of Arizona, Tucson 85721.

出版信息

Plant Dis. 2014 Oct;98(10):1447. doi: 10.1094/PDIS-04-14-0345-PDN.

Abstract

Cotton (Gossypium hirsutum L.) is an important and widely cultivated crop in Pakistan, upon which many rely for economic security. Cotton leaf curl disease (CLCuD) is caused by a complex comprising of more than eight species in the genus Begomovirus (family Geminiviridae) with associated betasatellite and alphasatellites. During 2011, characteristic symptoms of leaf curl disease were widespread (>40%), and the whitefly Bemisia tabaci (Genn.) vector of the leaf curl complex was abundant in commercial cotton fields in Burewala, Pakistan. Symptoms included vein thickening, upward or downward leaf curling, and foliar enations. To test for the presence of a begomovirus(es), total DNA was extracted from 100 mg of symptomatic leaf tissues from five different plants (isolates CLCuDBur1 to 5) using the CTAB method (1). Total DNA extracts were used for rolling circle amplification (RCA) using TempliPhi DNA Amplification Kit (GE Healthcare). Of the five field isolates, the RCA product for only one, CLCuDBur3, digested with HindIII, produced an apparently full-length ~2.7 kb fragment, suggesting that CLCuD-Bur3 represented a distinct isolate. The 2.7-kb fragment was cloned into the plasmid vector pGEM-3Zf+ (Promega, Madison, WI). To test for the presence of associated alphasatellites and betasatellites, the PCR primers, AlphaF/R and BetaF/R (2), were used to amplify the putative 1.4-kbp molecules. The resultant 1.4-kb PCR products were ligated into the pGEMT-Easy vector and cloned. Cloned inserts for each were subjected to DNA sequencing, bidirectionally. The cloned monopartite, helper begomovirus genome (HF567945), one betasatellite (HF567946), and one alphasatellite (HF567947) sequences were determined and found to be 2,742, 1,358, and 1,376 bases long, respectively. Pairwise sequence comparisons were carried out for each using the 10 most closely related species or strains (identified in GenBank using BLASTn) using MEGA5 software. The CLCuDBur3 genome sequence shared its highest identity (99.6%) with Okra enation leaf curl virus (OELCuV) (KC019308), so CLCuDBur3 is a variant of OELCuV, a begomovirus reported previously from Abelmoschus esculentus (L.) (okra) plants in India. The betasatellite and alphasatellite shared their highest nt identity at 96 and 98.7% with Cotton leaf curl Multan betasatellite (CLCuMB) (AM774311) and Cotton leaf curl Multan alphasatellite (CLCuMA), respectively (misnamed as CLCuBuA in GenBank) (FN658728). Additionally, the HindIII-digested RCA products were analyzed by Southern blot hybridization using a DIG-labeled DNA probe specific for the intergenic region of either Cotton leaf curl Burewala virus (CLCuBuV) or OELCuV. The OELCuV, but not the CLCuBuV, probe hybridized with HindIII digested RCA products (CLCuDBur3 genome), confirming the presence of OELCuV and the absence of CLCuBuV, the latter being the most prevalent begomovirus species infecting cotton in Pakistan. This is the first report of OELCuV infecting cotton plants in Pakistan, underscoring the discovery of yet another begomovirus member of the CLCuD complex. Further, the possible co-infection of cotton by OELCuV and other recognized species of the CLCuD complex could facilitate further diversification (potentially, through recombination) and lead to the emergence of new variants with the potential to cause damage to the cotton crop in Pakistan. References: (1) J. J. Doyle and J. L. Doyle. Focus. 12:13, 1990. (2) M. Zia-Ur-Rehman et al. Plant Dis. 97:1122, 2013.

摘要

棉花(陆地棉)是巴基斯坦一种重要且广泛种植的作物,许多人依靠它来保障经济安全。棉花卷叶病(CLCuD)由双生病毒科(Geminiviridae)菜豆金色花叶病毒属(Begomovirus)的八种以上病毒复合侵染引起,并伴有相关的β卫星和α卫星。2011年期间,卷叶病的典型症状广泛出现(超过40%),并且卷叶病毒复合体的粉虱传毒介体烟粉虱(Bemisia tabaci (Genn.))在巴基斯坦布勒瓦拉的商业棉田中大量存在。症状包括叶脉增厚、叶片向上或向下卷曲以及叶面瘤状突起。为检测是否存在菜豆金色花叶病毒,采用十六烷基三甲基溴化铵(CTAB)法(1)从五株不同植物(分离物CLCuDBur1至5)的100 mg有症状叶片组织中提取总DNA。总DNA提取物使用TempliPhi DNA扩增试剂盒(GE Healthcare)进行滚环扩增(RCA)。在五个田间分离物中,只有一个(CLCuDBur3)的RCA产物经HindIII酶切后产生了一个约2.7 kb的明显全长片段,这表明CLCuD - Bur3代表一个独特的分离物。将该2.7 kb片段克隆到质粒载体pGEM - 3Zf +(Promega,麦迪逊,威斯康星州)中。为检测相关α卫星和β卫星的存在,使用PCR引物AlphaF/R和BetaF/R(2)扩增推定的1.4 kbp分子。将得到的1.4 kb PCR产物连接到pGEMT - Easy载体中并进行克隆。对每个克隆的插入片段进行双向DNA测序。测定了克隆的单分体辅助菜豆金色花叶病毒基因组(HF567945)、一个β卫星(HF567946)和一个α卫星(HF567947)序列,发现它们分别长2742、1358和1376个碱基。使用MEGA5软件,将每个序列与10个最密切相关的物种或菌株(使用BLASTn在GenBank中鉴定)进行成对序列比较。CLCuDBur3基因组序列与秋葵瘤状叶卷曲病毒(OELCuV)(KC019308)的同源性最高(99.6%),因此CLCuDBur3是OELCuV的一个变种,OELCuV是先前在印度的黄秋葵(Abelmoschus esculentus (L.))植株中报道的一种菜豆金色花叶病毒。该β卫星和α卫星分别与棉花卷叶木尔坦β卫星(CLCuMB)(AM774311)和棉花卷叶木尔坦α卫星(CLCuMA)(在GenBank中错误命名为CLCuBuA)(FN658728)的核苷酸同源性最高,分别为96%和98.7%。此外,使用针对棉花卷叶布勒瓦拉病毒(CLCuBuV)或OELCuV基因间隔区的DIG标记DNA探针,通过Southern杂交分析HindIII酶切的RCA产物。OELCuV探针而非CLCuBuV探针与HindIII酶切的RCA产物(CLCuDBur3基因组)杂交,证实存在OELCuV且不存在CLCuBuV,CLCuBuV是巴基斯坦感染棉花的最普遍的菜豆金色花叶病毒种类。这是OELCuV感染巴基斯坦棉花植株的首次报道,强调了发现了棉花卷叶病复合体的又一个菜豆金色花叶病毒成员。此外,OELCuV与棉花卷叶病复合体其他公认病毒种类的可能共同侵染可能促进进一步的多样化(可能通过重组),并导致有可能对巴基斯坦棉花作物造成损害的新变种出现。参考文献:(1)J. J. Doyle和J. L. Doyle。《聚焦》。12:13,1990。(2)M. Zia - Ur - Rehman等人。《植物病害》。97:1122,2013。

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