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茄茉莉中马铃薯M病毒和菊花矮化类病毒的首次报道

First Report of Potato virus M and Chrysanthemum stunt viroid in Solanum jasminoides.

作者信息

Verhoeven J Th J, Jansen C C C, Roenhorst J W

机构信息

Plant Protection Service, Unit Virology, P.O. Box 9102, 6700 HC Wageningen, the Netherlands.

出版信息

Plant Dis. 2006 Oct;90(10):1359. doi: 10.1094/PD-90-1359A.

Abstract

In 2005, a plant of the ornamental crop Solanum jasminoides from the Netherlands was submitted for testing on viruses and viroids because of its intended use for propagation. Sap from this plant was mechanically inoculated to the test plant species Chenopodium quinoa, Nicotiana benthamiana, N. hesperis-67A, and N. occidentalis-P1 (3). N. hesperis-67A showed chlorotic local lesions and rugosity followed by vein necrosis, N. occidentalis-P1 showed necrotic local lesions and systemic leaf distortion, and the two other test plant species remained symptomless. Potato virus M (PVM) was identified by double antibody sandwich enzyme-linked immunosorbent assay using leaves from S. jasminoides and N. hesperis-67A. The plant of S. jasminoides was also tested for the presence of viroids by reverse transcriptase-polymerase chain reaction (RT-PCR) with universal pospiviroid primers Pospi1-RE/FW (2). This reaction yielded an amplicon of the expected size of 198 bp. The sequence showed 100% identity to an isolate of Chrysanthemum stunt viroid (CSVd; NCBI GenBank Accession No. AF394453). Subsequently, the complete sequence of our viroid isolate (GenBank Accession No. DQ406591) was determined from the amplicon obtained after RT-PCR using specific primers for the detection of CSVd (1). The viroid isolate from S. jasminoides consisted of 354 nucleotides and showed the highest identity (98.6%) to a chrysanthemum isolate of CSVd (GenBank Accession No. AB055974). Therefore, the viroid was identified as CSVd. To our knowledge, this is the first report of PVM and CSVd in S. jasminoides. Reference: (1) R. Hooftman et al. Acta Hortic. 432:120, 1996. (2) J. Th. J. Verhoeven et al. Eur. J. Plant Pathol. 110:823, 2004. (3) J. Th. J. Verhoeven and J. W. Roenhorst, EPPO Bull. 33:305, 2003.

摘要

2005年,一株来自荷兰的观赏作物茉莉茄因其用于繁殖的预期用途而被提交进行病毒和类病毒检测。将该植物的汁液机械接种到藜麦、本氏烟草、N. hesperis - 67A和N. occidentalis - P1这几种测试植物上(3)。N. hesperis - 67A出现褪绿局部病斑和皱缩,随后叶脉坏死;N. occidentalis - P1出现坏死局部病斑和系统性叶片扭曲;另外两种测试植物则无症状。使用来自茉莉茄和N. hesperis - 67A的叶片,通过双抗体夹心酶联免疫吸附测定法鉴定出马铃薯M病毒(PVM)。还使用通用马铃薯纺锤块茎类病毒引物Pospi1 - RE/FW,通过逆转录聚合酶链反应(RT - PCR)对茉莉茄植株进行类病毒检测(2)。该反应产生了预期大小为198 bp的扩增子。序列分析显示其与菊花矮化类病毒(CSVd;NCBI基因库登录号AF394453)的一个分离株具有100%的同一性。随后,使用用于检测CSVd的特异性引物,从RT - PCR后获得的扩增子中确定了我们的类病毒分离株的完整序列(1)。来自茉莉茄的类病毒分离株由354个核苷酸组成,与CSVd的一个菊花分离株(基因库登录号AB055974)具有最高的同一性(98.6%)。因此,该类病毒被鉴定为CSVd。据我们所知,这是关于茉莉茄中PVM和CSVd的首次报道。参考文献:(1) R. Hooftman等人,《园艺学报》432:120,1996年。(2) J. Th. J. Verhoeven等人,《欧洲植物病理学报》110:823,2004年。(X) J. Th. J. Verhoeven和J. W. Roenhorst,《欧洲和地中海植物保护组织通报》33:305,2003年。 (注:原文中的(X)在中文里无对应,可能是编号错误之类的,这里保留原样)

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