Ammara U E, Al-Shihi A, Amin I, Al-Sadi A M
Department of Crop Sciences, College of Agricultural and Marine Sciences, Sultan Qaboos University, Al-Khod 123, Oman.
Agricultural Biotechnology Division, National Institute for Biotechnology and Genetic Engineering (NIBGE), Faisalabad, Pakistan.
Plant Dis. 2015 Mar;99(3):421. doi: 10.1094/PDIS-09-14-0912-PDN.
Leaf curl disease with severe curling, vein darkening, and vein thickening was observed on papaya plants in a field in Qurayat district of Oman during December 2013. Disease incidence ranged from 50 to 70%, particularly in young papaya plants. The presence of a large population of whiteflies and symptoms observed on papaya plants suggested that the causal agent could be begomoviruses (family Geminiviridae) and associated satellites. Four leaf samples with mild and severe leaf curling were collected from the field. Total nucleic acid extracted from symptomatic and healthy plants using the CTAB method were used as a template to amplify circular DNAs using Φ29 DNA polymerase, and products were digested with restriction enzymes to identify fragments of 2.6 to 2.8 kb typical of geminiviruses. BamHI yielded fragments of ~2.8 and 1.4 kb when the digested products were resolved by electrophoresis on a 1% agarose gel. These fragments were cloned and sequenced using a primer walking strategy in both directions. Sequencing results confirmed the exact sizes of 1,303, 1,358, and 2,765 bp; the sequences were deposited in GenBank under the accession numbers HG969296, HG969297, and HG969260, respectively. BLAST results showed that the first two sequences are Tomato leaf curl betasatellite (ToLCB; isolates Pap-2 and Pap-3) showing 97% sequence identity with a previously reported ToLCB sequence (Accession No. KF229728). Both satellites encode a single gene in the complementary sense strand referred to as βC1, which showed 97% sequence identity to ToLCB (HE800551). The viral sequence (isolate Pap-6) showed four genes in the complementary sense (the replication-associated protein [Rep] gene, the transcription-activator protein [TrAP] gene, the replication-enhancer protein [REn] gene, and the C4 gene) and two genes (pre-coat protein [V2] and coat protein [CP]) in virion-sense (2). BLAST analysis showed 95.2% sequence identity to Tomato leaf curl Albatinah virus (ToLCABV; FJ956700), reported earlier to infect tomato in Oman (3). Amino acid sequence comparison of the four predicted proteins (Rep, TrAP, Ren, and C4) encoded by Pap-6 shared 95, 96, 100, and 100% sequence identity, whereas virion-sense proteins (V1 and V2) shared 99% sequence identity with ToLCABV (FJ956700). According to the recommendations of the International Committee on Taxonomy of Viruses, these results indicate that the virus identified in association with papaya leaf curl disease in Oman is a variant of ToLCABV (1). All infected samples showed the presence of ToLCABV, while no hybridization was observed in healthy control DNA using ToLCABV probe. These findings are indicative of the rapid spread of diseases involving Begomovirus and betasatellites, which often result in increased host range, as is evident from this study. References: (1) C. M. Fauquet et al. Arch. Virol. 148:405, 2003. (2) L. Hanley-Bowdoin et al. Crit. Rev. Plant Sci. 18:71, 1999. (3) A. J. Khan et al. Arch. Virol. 159:445, 2013.
2013年12月,在阿曼库赖亚特地区的一块农田里,木瓜植株上出现了叶片卷曲病,症状表现为严重卷曲、叶脉变黑和叶脉增粗。发病率在50%至70%之间,尤其在幼嫩木瓜植株中更为明显。木瓜植株上大量烟粉虱的存在以及观察到的症状表明,致病因子可能是双生病毒科(Geminiviridae)的菜豆金色花叶病毒属病毒(begomoviruses)及其相关卫星分子。从田间采集了四个有轻度和重度叶片卷曲症状的叶片样本。使用CTAB法从有症状和健康的植株中提取总核酸,以此作为模板,用Φ29 DNA聚合酶扩增环状DNA,然后用限制性内切酶消化产物,以鉴定双生病毒典型的2.6至2.8 kb片段。当消化产物在1%琼脂糖凝胶上进行电泳分离时,BamHI产生了约2.8 kb和1.4 kb的片段。这些片段通过双向引物步移策略进行克隆和测序。测序结果证实了片段的确切大小分别为1303、1358和2765 bp;这些序列分别以登录号HG969296、HG969297和HG969260存入GenBank。BLAST结果显示,前两个序列是番茄卷叶β卫星分子(ToLCB;分离株Pap - 2和Pap - 3),与先前报道的ToLCB序列(登录号KF229728)具有97%的序列同一性。这两个卫星分子在互补链上编码一个单一基因,称为βC1,与ToLCB(HE800551)具有97%的序列同一性。病毒序列(分离株Pap - 6)在互补链上显示有四个基因(复制相关蛋白[Rep]基因、转录激活蛋白[TrAP]基因、复制增强蛋白[REn]基因和C4基因),在病毒链上有两个基因(前衣壳蛋白[V2]和衣壳蛋白[CP])。BLAST分析显示,与番茄卷叶阿尔巴蒂纳病毒(ToLCABV;FJ956700)具有95.