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波兰甜菜土壤传播病毒的首次报告。

First Report of Beet soilborne virus in Poland.

作者信息

Borodynko N, Hasiów B, Pospieszny H

机构信息

Institute of Plant Protection, Department of Virology and Bacteriology, Miczurina 20, 60-318 Pozna, Poland.

出版信息

Plant Dis. 2006 Jan;90(1):112. doi: 10.1094/PD-90-0112B.

Abstract

Beet necrotic yellow vein virus (BNYVV), the casual agent of rhizomania disease, was identified in sugar beet plants from several fields in the Wielkopolska Region of Poland (1). In greenhouse studies, sugar beets were grown in the soil from one of these fields to bait soilborne viruses. Of 200 sugar beet plants, three developed symptoms of vein clearing, vein banding, and mosaic. Crude sap from symptomatic plants was used for mechanical inoculation of various plants species. In Chenopodium quinoa, C. amaranticolor, and Tetragonia expansa only local lesions were observed. Electron microscope examination of negatively stained leaf-dip preparations from symptomatic sugar beet plants showed a mixture of rod-shape particles from 70 to 400 nm long. Using double-antibody sandwich enzyme-linked immunosorbent assay tests, two symptomatic sugar beet plants gave positive reactions with antiserum against BNYVV (Bio-Rad, Hercules, CA) and a third plant gave a positive reaction with antisera against BNYVV and Beet soilborne virus (BSBV). Total RNA was extracted from roots and leaves of the symptomatic plants and used in a multiplex reverse transcription-polymerase chain reaction (mRT-PCR) assay. Specific primers were designed to amplify a fragment of the RNA1 for BSBV and RNA2 for BNYVV and Beet virus Q (BVQ) (2). Two mRT-PCR products amplified with the primers specific to BNYVV and BSBV were obtained and sequenced. A 274-nt amplicon sequence (GenBank Accession No. DQ012156) had 98% nucleotide sequence identity with the German BNYVV isolate F75 (GenBank Accession No. AF19754) and a 376-nt amplicon sequence (GenBank Accession No. AY999690) had 98% nucleotide and 98% amino acid sequence identity with the German BSBV isolate (GenBank Accession No. Z97873). The Polish BSBV isolate had 88% nucleotide and 62% amino acid sequence identity with BVQ, another pomovirus (GenBank Accession No. AJ 223596 formerly known as serotype Wierthe of BSBV (2). In 2005, mRT-PCR was used on samples collected from two fields of the Wielkopolska Region. Of 15 tested sugar beet plants, 12 gave positive reactions with primers specific for BSBV and nine with primers specific to BNYVV. To our knowledge, this is first report of BSBV in Poland. In Europe, BSBV was previously reported in England, the Netherlands, Belgium, Sweden, Germany, France, and Finland (2,3). References: (1) M. Jezewska and J. Piszczek. Phytopathol. Polonica, 21:165, 2001. (2) A. Maunier et al. Appl. Environ. Microbiol. 69:2356, 2003. (3) C. M. Rush and G. B. Heidel. Plant Dis. 79:868, 1995.

摘要

甜菜坏死黄脉病毒(BNYVV)是根肿病的致病因子,在波兰大波兰地区多个田地的甜菜植株中被发现(1)。在温室研究中,将甜菜种植在其中一块田地的土壤中,以诱捕土壤传播的病毒。在200株甜菜植株中,有三株出现了叶脉黄化、叶脉带状和花叶症状。将有症状植株的粗汁液用于对多种植物进行机械接种。在藜、苋色藜和番杏中仅观察到局部病斑。对有症状甜菜植株的负染色叶浸液制剂进行电子显微镜检查,发现有长度为70至400纳米的杆状颗粒混合物。使用双抗体夹心酶联免疫吸附测定试验,两株有症状的甜菜植株与抗BNYVV抗血清(Bio-Rad,美国加利福尼亚州赫拉克勒斯)呈阳性反应,第三株植株与抗BNYVV抗血清和甜菜土壤传播病毒(BSBV)抗血清均呈阳性反应。从有症状植株的根和叶中提取总RNA,并用于多重逆转录-聚合酶链反应(mRT-PCR)分析。设计了特异性引物,用于扩增BSBV的RNA1片段以及BNYVV和甜菜病毒Q(BVQ)的RNA2片段(2)。获得了用BNYVV和BSBV特异性引物扩增的两个mRT-PCR产物并进行了测序。一个274个核苷酸的扩增子序列(GenBank登录号DQ012156)与德国BNYVV分离株F75(GenBank登录号AF19754)的核苷酸序列同一性为98%,一个376个核苷酸的扩增子序列(GenBank登录号AY999690)与德国BSBV分离株(GenBank登录号Z97873)的核苷酸和氨基酸序列同一性均为98%。波兰的BSBV分离株与另一种马铃薯Y病毒属病毒BVQ(GenBank登录号AJ 223596,以前称为BSBV的Wierthe血清型(2))的核苷酸序列同一性为88%,氨基酸序列同一性为62%。2005年,对从大波兰地区两块田地采集的样本进行了mRT-PCR检测。在15株检测的甜菜植株中,12株对BSBV特异性引物呈阳性反应,9株对BNYVV特异性引物呈阳性反应。据我们所知,这是BSBV在波兰的首次报道。在欧洲,此前在英国、荷兰、比利时、瑞典、德国、法国和芬兰报道过BSBV(2,3)。参考文献:(1)M. Jezewska和J. Piszczek。《波兰植物病理学》,21:165,2001。(2)A. Maunier等人。《应用与环境微生物学》,69:2356,2003。(3)C. M. Rush和G. B. Heidel。《植物病害》,79:868,199

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