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多米尼加共和国田间番茄自然感染马铃薯纺锤块茎类病毒的首次报道。

First Report of Potato spindle tuber viroid Naturally Infecting Field Tomatoes in the Dominican Republic.

作者信息

Ling K-S, Li R, Groth-Helms D, Assis-Filho F M

机构信息

USDA-ARS, U.S. Vegetable Laboratory, Charleston, SC 29414.

Agdia Inc., Elkhart, IN 46514.

出版信息

Plant Dis. 2014 May;98(5):701. doi: 10.1094/PDIS-09-13-0992-PDN.

Abstract

In recent years, viroid disease outbreaks have resulted in serious economic losses to a number of tomato growers in North America (1,2,3). At least three pospiviroids have been identified as the causal agents of tomato disease, including Potato spindle tuber viroid (PSTVd), Tomato chlorotic dwarf viroid (TCDVd), and Mexican papita viroid (MPVd). In the spring of 2013, a severe disease outbreak with virus-like symptoms (chlorosis and plant stunting) was observed in a tomato field located in the Dominican Republic, whose tomato production is generally exported to the United States in the winter months. The transplants were produced in house. The disease has reached an epidemic level with many diseased plants pulled and disposed of accordingly. Three samples collected in May of 2013 were screened by ELISA against 16 common tomato viruses (Alfalfa mosaic virus, Cucumber mosaic virus, Impatiens necrotic spot virus, Pepino mosaic virus, Potato virus X, Potato virus Y, Tobacco etch virus, Tobacco mosaic virus, Tobacco ringspot virus, Tomato aspermy virus, Tomato bushy stunt virus, Tomato mosaic virus, Tomato ringspot virus, Tomato spotted wilt virus, Groundnut ringspot virus, and Tomato chlorotic spot virus), a virus group (Potyvirus group), three bacteria (Clavibacter michiganensis subsp. michiganensis, Pectobacterium atrosepticum, and Xanthomonas spp.), and Phytophthora spp. No positive result was observed, despite the presence of symptoms typical of a viral-like disease. Further analysis by RT-PCR using Agdia's proprietary pospiviroid group-specific primer resulted in positive reactions in all three samples. To determine which species of pospiviroid was present in these tomato samples, full-genomic products of the expected size (~360 bp) were amplified by RT-PCR using specific primers for PSTVd (4) and cloned using TOPO-TA cloning kit (Invitrogen, CA). A total of 8 to 10 clones from each isolate were selected for sequencing. Sequences from each clone were nearly identical and the predominant sequence DR13-01 was deposited in GenBank (Accession No. KF683200). BLASTn searches into the NCBI database demonstrated that isolate DR13-01 shared 97% sequence identity to PSTVd isolates identified in wild Solanum (U51895), cape gooseberry (EU862231), or pepper (AY532803), and 96% identity to the tomato-infecting PSTVd isolate from the United States (JX280944). The relatively lower genome sequence identity (96%) to the tomato-infecting PSTVd isolate in the United States (JX280944) suggests that PSTVd from the Dominican Republic was likely introduced from a different source, although the exact source that resulted in the current disease outbreak remains unknown. It may be the result of an inadvertent introduction of contaminated tomato seed lots or simply from local wild plants. Further investigation is necessary to determine the likely source and route of introduction of PSTVd identified in the current epidemic. Thus, proper control measures could be recommended for disease management. The detection of this viroid disease outbreak in the Dominican Republic represents further geographic expansion of the viroid disease in tomatoes beyond North America. References: (1). K.-S. Ling and M. Bledsoe. Plant Dis. 93:839, 2009. (2) K.-S. Ling and W. Zhang. Plant Dis. 93:1216, 2009. (3) K.-S. Ling et al. Plant Dis. 93:1075, 2009. (4) A. M. Shamloul et al. Can. J. Plant Pathol. 19:89, 1997.

摘要

近年来,类病毒病的爆发给北美的一些番茄种植者造成了严重的经济损失(1,2,3)。至少有三种马铃薯纺锤块茎类病毒被确定为番茄疾病的病原体,包括马铃薯纺锤块茎类病毒(PSTVd)、番茄褪绿矮缩类病毒(TCDVd)和墨西哥番木瓜类病毒(MPVd)。2013年春季,在多米尼加共和国的一个番茄田中观察到了一次严重的疾病爆发,出现了类似病毒的症状(黄化和植株矮化),该国的番茄产量通常在冬季出口到美国。这些移植苗是在当地培育的。这种疾病已经达到了流行程度,许多患病植株被拔除并进行了相应处理。2013年5月采集的三个样本通过酶联免疫吸附测定(ELISA)针对16种常见的番茄病毒(苜蓿花叶病毒、黄瓜花叶病毒、凤仙坏死斑病毒、佩佩诺花叶病毒、马铃薯X病毒、马铃薯Y病毒、烟草蚀纹病毒、烟草花叶病毒、烟草环斑病毒、番茄不孕病毒、番茄丛矮病毒、番茄花叶病毒、番茄环斑病毒、番茄斑萎病毒、花生环斑病毒和番茄褪绿斑病毒)、一个病毒组(马铃薯Y病毒组)、三种细菌(密执安棒形杆菌密执安亚种、黑胫果胶杆菌和黄单胞菌属)以及疫霉属进行了检测。尽管存在类似病毒疾病的典型症状,但未观察到阳性结果。使用艾迪亚公司专有的马铃薯纺锤块茎类病毒组特异性引物通过逆转录聚合酶链反应(RT-PCR)进行的进一步分析在所有三个样本中均产生了阳性反应。为了确定这些番茄样本中存在哪种马铃薯纺锤块茎类病毒,使用针对PSTVd的特异性引物通过RT-PCR扩增出预期大小(约360 bp)的全基因组产物,并使用TOPO-TA克隆试剂盒(Invitrogen,加利福尼亚州)进行克隆。从每个分离株中总共选择8至10个克隆进行测序。每个克隆的序列几乎相同,主要序列DR13-01已存入GenBank(登录号KF683200)。在NCBI数据库中进行的BLASTn搜索表明,分离株DR13-01与在野生茄属植物(U51895)、灯笼果(EU862231)或辣椒(AY532803)中鉴定出的PSTVd分离株具有97%的序列同一性,与来自美国的感染番茄的PSTVd分离株(JX280944)具有96%的同一性。与来自美国的感染番茄的PSTVd分离株(JX280944)相对较低的基因组序列同一性(96%)表明,来自多米尼加共和国的PSTVd可能是从不同来源引入的,尽管导致当前疾病爆发的确切来源仍然未知。这可能是无意中引入受污染的番茄种子批次的结果,或者仅仅是来自当地野生植物。有必要进行进一步调查以确定当前疫情中鉴定出的PSTVd的可能来源和引入途径。因此,可以推荐适当的控制措施来进行疾病管理。在多米尼加共和国检测到这种类病毒病的爆发代表了类病毒病在番茄中超出北美范围的进一步地理扩展。参考文献:(1)。K.-S. Ling和M. Bledsoe。植物病害。93:第839页,2年。(2)K.-S. Ling和W. Zhang。植物病害。93:第1216页,2009年。(3)K.-S. Ling等人。植物病害。93:第1075页,2009年。(4)A. M. Shamloul等人。加拿大植物病理学杂志。19:第89页,1997年。

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