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黄瓜花叶病毒亚组II在印度侵染番茄的首次报道。

First Report of Cucumber mosaic virus Subgroup II Infecting Lycopersicon esculentum in India.

作者信息

Sudhakar N, Nagendra-Prasad D, Mohan N, Murugesan K

机构信息

Centre for Advanced Studies in Botany, University of Madras, Guindy campus, Chennai-600 025, India.

出版信息

Plant Dis. 2006 Nov;90(11):1457. doi: 10.1094/PD-90-1457B.

Abstract

During a survey in January 2006 near Salem in Tamil Nadu (south India), Cucumber mosaic virus was observed infecting tomatoes with an incidence of more than 70%. Plants exhibiting severe mosaic, leaf puckering, and stunted growth were collected, and the virus was identified using diagnostic hosts, evaluation of physical properties of the virus, compound enzyme-linked immunosorbent assay (ELISA) (ELISA Lab, Washington State University, Prosser), reverse-transcription polymerase chain reaction (RT-PCR), and restriction fragment length polymorphism analysis (DSMZ, S. Winter, Germany). To determine the specific CMV subgroup, total RNA was extracted from 50 infected leaf samples using the RNeasy plant RNA isolation kit (Qiagen, Hilden, Germany) and tested for the presence of the complete CMV coat protein gene using specific primers as described by Rizos et al. (1). A fragment of the coat protein was amplified and subsequently digested with MspI to reveal a pattern of two fragments (336 and 538 bp), indicating CMV subgroup II. No evidence of mixed infection with CMV subgroup I was obtained when CMV isolates representing subgroups I (PV-0419) and II (PV-0420), available at the DSMZ Plant Virus Collection, were used as controls. Only CMV subgroup I has been found to predominantly infect tomato in the Indian subcontinent, although Verma et al. (2) identified CMV subgroup II infecting Pelargonium spp., an ornamental plant. To our knowledge, this is the first report of CMV subgroup II infecting tomato crops in India. References: (1) H. Rizos et al. J. Gen. Virol. 73:2099, 1992. (2) N. Verma et al. J. Biol. Sci. 31:47, 2006.

摘要

2006年1月在印度南部泰米尔纳德邦塞勒姆附近进行的一项调查中,发现黄瓜花叶病毒感染番茄,发病率超过70%。采集了表现出严重花叶、叶片皱缩和生长受阻的植株,利用诊断寄主、病毒物理特性评估、复合酶联免疫吸附测定(ELISA)(华盛顿州立大学普罗瑟分校ELISA实验室)、逆转录聚合酶链反应(RT-PCR)以及限制性片段长度多态性分析(德国DSMZ的S. Winter)对病毒进行鉴定。为确定黄瓜花叶病毒的具体亚组,使用RNeasy植物RNA提取试剂盒(德国希尔德的Qiagen公司)从50个受感染叶片样本中提取总RNA,并按照Rizos等人(1)所述,使用特异性引物检测完整的黄瓜花叶病毒外壳蛋白基因的存在。扩增外壳蛋白的一个片段,随后用MspI酶切,显示出两条片段(336和5

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