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番木瓜环斑病毒侵染波兰西葫芦植株的首次报道。

First Report of Papaya ringspot virus Infecting Zucchini Plants in Poland.

作者信息

Hasiów-Jaroszewska B, Borodynko N, Rymelska N, Pospieszny H

机构信息

Institute of Plant Protection-National Research Institute, Department of Virology and Bacteriology, W. Węgorka 20, 60-318 Poznań, Poland.

出版信息

Plant Dis. 2010 May;94(5):633. doi: 10.1094/PDIS-94-5-0633C.

Abstract

Papaya ringspot virus (PRSV), a member of the aphid-transmitted genus Potyvirus, is the cause of a destructive disease and a major limiting factor for papaya and cucurbit cultivation worldwide. The virus occurs in China, France, Germany, India, Italy, Mexico, Taiwan, and the United States. Its P biotype is a devastating pathogen of papaya crops and its W biotype is a pathogen of cucurbits (4). In 2009, zucchini plants with leaf mosaic and marbled fruit were collected from the Kujawsko-Pomorskie Region of Poland. Samples came from the same region where Zucchini yellow mosaic virus (ZYMV) (3) and Watermelon mosaic virus (WMV) (1) have been found previously. Forty leaf and ten fruit samples of zucchini (Cucurbita pepo cv. giromontina) were tested by double-antibody sandwich (DAS)-ELISA with commercial antisera against WMV, ZYMV, and PRSV (DSMZ, Braunschweig, Germany). PRSV was found in two samples tested. Leaf extracts from infected plants were mechanically inoculated onto Carborundum-dusted leaves of the following indicator plants: Cucumis sativus, Chenopodium quinoa, Cucurbita pepo, Nicotiana benthamiana, and N. tabacum cv. Xanthi. After 2 weeks, symptoms of leaf chlorosis on cucumber and chlorotic lesions on zucchini were observed. Total RNA was extracted from infected leaves with a phenol-chloroform based extraction procedure. The presence of PRSV was confirmed by reverse transcription (RT)-PCR reaction using primers 04-02 and 04-04, which amplify the coat protein gene (2). Amplified DNA was gel purified with a Qiaex Kit (Qiagen, Valencia, CA) and cloned into pGEM-T easy (Promega, Madison, WI). Overlapping sequences were obtained using universal M13F and M13R primers. BioEdit software ( http://www.mbio.ncsu.edu/BioEdit/bioedit.html ) was used to assemble the nucleotide consensus sequence. The obtained sequence (861 bp encoding 287 amino acids) was deposited in the GenBank database under Accession No. GQ927328. The comparison with PRSV sequences retrieved from the GenBank database were carried out to investigate the genetic diversity between Polish PRSV isolates and establish their molecular relationships to the previously characterized PRSV isolates from different parts of the world. The sequences of PRSV Polish isolates obtained from two infected plant samples were identical. Comparisons revealed that the Polish isolate designated PRSV-BON shared the highest identity (97%) with three Australian isolates (U14739, U14740, and U14744). To our knowledge, this is the first report of PRSV infecting zucchini plants in Poland. The occurrence of subtropic viruses like PRSV in Poland indicated the introduction of new pathogens that likely affect cucurbit production in this country and beyond. References: (1) N. Borodynko et al. Plant Pathol. 58:783, 2009. (2) M. Chin et al. Arch. Virol. 152:2101, 2007. (3) H. Pospieszny et al. Plant Dis. 91:639, 2007. (4) D. J. Purcifull et al. CMI/AAB Descriptions of Plant Viruses. No. 292, 1984.

摘要

番木瓜环斑病毒(PRSV)是由蚜虫传播的马铃薯Y病毒属成员,是一种毁灭性病害的病原体,也是全球番木瓜和葫芦科作物种植的主要限制因素。该病毒在中国、法国、德国、印度、意大利、墨西哥、台湾和美国均有发生。其P生物型是番木瓜作物的毁灭性病原体,W生物型是葫芦科作物的病原体(4)。2009年,从波兰库亚维-波美拉尼亚地区采集了出现叶片花叶和果实大理石花纹症状的西葫芦植株。样本来自之前发现过西葫芦黄花叶病毒(ZYMV)(3)和西瓜花叶病毒(WMV)(1)的同一地区。用针对WMV、ZYMV和PRSV的商业抗血清,通过双抗体夹心(DAS)-ELISA法对40份西葫芦(Cucurbita pepo cv. giromontina)叶片样本和10份果实样本进行检测(德国不伦瑞克的德国微生物和细胞培养物保藏中心)。在检测的两份样本中发现了PRSV。将感染植株的叶片提取物机械接种到以下指示植物经金刚砂摩擦处理的叶片上:黄瓜、藜麦、西葫芦、本氏烟草和烟草品种Xanthi。2周后,观察到黄瓜叶片褪绿症状和西葫芦叶片褪绿斑。用基于苯酚-氯仿的提取方法从感染叶片中提取总RNA。使用引物04-02和04-04通过逆转录(RT)-PCR反应确认PRSV的存在,这对引物扩增外壳蛋白基因(2)。用Qiaex试剂盒(Qiagen公司,加利福尼亚州瓦伦西亚)对扩增的DNA进行凝胶纯化,并克隆到pGEM-T easy载体(Promega公司,威斯康星州麦迪逊)中。使用通用M13F和M13R引物获得重叠序列。使用BioEdit软件(http://www.mbio.ncsu.edu/BioEdit/bioedit.html)组装核苷酸共有序列。获得的序列(861 bp,编码287个氨基酸)已存入GenBank数据库,登录号为GQ927328。与从GenBank数据库检索到的PRSV序列进行比较,以研究波兰PRSV分离株之间的遗传多样性,并确定它们与世界不同地区先前鉴定的PRSV分离株的分子关系。从两份感染植株样本中获得的波兰PRSV分离株序列相同。比较结果显示,命名为PRSV-BON的波兰分离株与三份澳大利亚分离株(U14739、U14740和U14744)的同源性最高(97%)。据我们所知,这是PRSV在波兰感染西葫芦植株的首次报道。像PRSV这样的亚热带病毒在波兰出现,表明引入了可能影响该国及其他地区葫芦科作物生产的新病原体。参考文献:(1)N. Borodynko等人,《植物病理学》58:783,2009年。(2)M. Chin等人,《病毒学档案》152:2101,2007年。(3)H. Pospieszny等人,《植物病害》91:639,2007年。(4)D. J. Purcifull等人,《CMI/AAB植物病毒描述》,第292号,1984年。

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