Suppr超能文献

在巴基斯坦有症状的丝瓜中首次检测到棉花曲叶布尔埃瓦拉病毒及其同源的棉花曲叶木尔坦β卫星和达尔文棉无症状α卫星。

First Detection of Cotton leaf curl Burewala virus and Cognate Cotton leaf curl Multan betasatellite and Gossypium darwinii symptomless alphasatellite in Symptomatic Luffa cylindrica in Pakistan.

作者信息

Zia-Ur-Rehman M, Herrmann H-W, Hameed U, 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. 2013 Aug;97(8):1122. doi: 10.1094/PDIS-12-12-1159-PDN.

Abstract

Cotton leaf curl disease (CLCuD) is the major plant viral constraint to cotton production on the Indian subcontinent (2). CLCuD is primarily caused by begomovirus, Cotton leaf curl Burewala virus (CLCuBuV), and Cotton leaf curl Multan betasatellite (CLCuMB). During 2011 in Burewala, Pakistan, plants in a production field of Luffa cylindrica (Ghia tori) were infested with the whitefly Bemisia tabaci (Genn.), and ~60% of the plants exhibited leaf curling and stunting symptoms, reminiscent of those caused by begomoviruses (Geminiviridae). Total DNA was extracted from five different symptomatic leaf samples using the CTAB method (1), and extracts were analyzed by Southern blot hybridization. As a probe, we used a 1.1-kbp fragment of CLCuBuV and a positive signal was obtained from all five samples. Total DNA was used as template for rolling circle amplification (RCA) using the TempliPhi DNA Amplification Kit (GE Healthcare, Little Chalfont, United Kingdom). The amplified RCA products were digested with EcoRI, and the resulting ~2.7-kbp fragments from each isolate were directionally cloned into the EcoRI digested, pGEM-3Zf+ (Promega, Madison, WI) plasmid vector. PCR was used to amplify the prospective, associated betasatellite and alphasatellite molecules using the primers BetaF5'-GGTACCGCCGGAGCTTAGCWCKCC-3' and BetaR5'-GGTACCGTAGCTAAGGCTGCTGCG-3', and AlphaF5'-AAGCTTAGAGGAAACTAGGGTTTC-3' and AlphaR5'-AAGCTTTTCATACARTARTCNCRDG-3', respectively. The putative satellite amplicons, at ~1.4 kbp each were cloned in the plasmid vector pGEMT-Easy (Promega, Madison, WI) and sequenced. BLASTn comparisons of the apparently full-length begomoviral genomes, at 2,753 nt, against the NCBI database revealed that all five isolates were most closely related to CLCuBuV (FR750321). In addition, one each of beta- and alpha-satellite were amplified from all five samples at 1,393 and 1,378 bases, respectively. The beta- and alpha-satellites were most closely related to CLCuMB (HE985228) and the Gossypium darwinii symptomless alphasatellite (GDaSA) (FR877533), respectively. Pairwise sequence comparisons of the top 10 BLASTn hits using MEGA5 indicated that the helper begomovirus shared 99.9% identity with CLCuBuV (FR750321), the most prevalent helper virus currently associated with the leaf curl complex in Pakistan. Based on the ICTV demarcation for begomoviral species at <89%, it is considered a variant of CLCuBuV. The resultant beta- and alpha-satellite sequences were 98.1% and 97.8% identical to CLCuMB (HE985228) and GDaSA (FR877533), respectively, and are the most prevalent satellites associated with the CLCuD complex in Pakistan and India (2). To our knowledge, this is first report of the CLCuBuV-CLCuMB-GDaSA complex infecting a cucurbitaceous species, and the first report of L. cylindrica as a host of the CLCuD complex. This discovery of CLCuBuV and associated satellites in a cucurbitaceous host that is widely grown in Pakistan and India where this complex infects cotton indicates that the host range of CLCuBuV is broader than expected. This new information will aid in better understanding of cotton leaf curl disease epidemiology in the current epidemic areas. References: (1) J. J. Doyle and J. L. Doyle. Focus 12:13, 1990. (2) S. Mansoor et al. Trends Plant Sci. 11:209, 2006.

摘要

棉花卷叶病(CLCuD)是印度次大陆棉花生产面临的主要植物病毒制约因素(2)。CLCuD主要由双生病毒、棉花卷叶布尔埃瓦拉病毒(CLCuBuV)和棉花卷叶木尔坦β卫星(CLCuMB)引起。2011年在巴基斯坦布尔埃瓦拉,丝瓜(Ghia tori)生产田中的植株受到烟粉虱(Bemisia tabaci (Genn.))侵害,约60%的植株出现叶片卷曲和发育迟缓症状,类似于双生病毒(双生病毒科)引起的症状。使用CTAB法(1)从五个不同的有症状叶片样本中提取总DNA,并通过Southern杂交分析提取物。作为探针,我们使用了CLCuBuV的一个1.1 kbp片段,所有五个样本均获得阳性信号。以总DNA为模板,使用TempliPhi DNA扩增试剂盒(通用电气医疗集团,英国小查尔方特)进行滚环扩增(RCA)。将扩增的RCA产物用EcoRI消化,每个分离株产生的约2.7 kbp片段定向克隆到用EcoRI消化的pGEM-3Zf+(普洛麦格公司,威斯康星州麦迪逊)质粒载体中。使用引物BetaF 5'-GGTACCGCCGGAGCTTAGCWCKCC-3'和BetaR 5'-GGTACCGTAGCTAAGGCTGCTGCG-3',以及AlphaF 5'-AAGCTTAGAGGAAACTAGGGTTTC-3'和AlphaR 5'-AAGCTTTTCATACARTARTCNCRDG-3',分别通过PCR扩增预期的相关β卫星和α卫星分子。推定的卫星扩增子各约1.4 kbp,克隆到质粒载体pGEMT-Easy(普洛麦格公司,威斯康星州麦迪逊)中并测序。将长度为2753 nt的明显全长双生病毒基因组与NCBI数据库进行BLASTn比较,结果显示所有五个分离株与CLCuBuV(FR750321)关系最为密切。此外,从所有五个样本中分别扩增出一个β卫星和一个α卫星,长度分别为1393和1378个碱基。β卫星和α卫星分别与CLCuMB(HE985228)和达尔文棉无症状α卫星(GDaSA)(FR877533)关系最为密切。使用MEGA5对前10个BLASTn比对结果进行成对序列比较表明,辅助双生病毒与CLCuBuV(FR750321)的同一性为99.9%,CLCuBuV是目前与巴基斯坦卷叶复合体相关的最普遍辅助病毒。根据国际病毒分类委员会对双生病毒种的划分标准(<89%),它被认为是CLCuBuV的一个变种。所得的β卫星和α卫星序列分别与CLCuMB(HE985228)和GDaSA(FR877533)的同一性为98.1%和97.8%,是巴基斯坦和印度与CLCuD复合体相关的最普遍卫星(2)。据我们所知,这是关于CLCuBuV-CLCuMB-GDaSA复合体感染葫芦科物种的首次报道,也是丝瓜作为CLCuD复合体宿主的首次报道。在巴基斯坦和印度广泛种植的葫芦科宿主中发现CLCuBuV及其相关卫星,而该复合体在当地感染棉花,这表明CLCuBuV的宿主范围比预期更广。这些新信息将有助于更好地了解当前疫区的棉花卷叶病流行病学。参考文献:(1)J. J. Doyle和J. L. Doyle。《聚焦》12:13,1990。(2)S. Mansoor等人。《植物科学趋势》11:209,2006。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验