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通过小RNA深度测序增强对来自洪都拉斯和危地马拉甘薯中病毒的检测

Detection of Viruses in Sweetpotato from Honduras and Guatemala Augmented by Deep-Sequencing of Small-RNAs.

作者信息

Kashif M, Pietilä S, Artola K, Jones R A C, Tugume A K, Mäkinen V, Valkonen J P T

机构信息

Department of Agricultural Sciences, FI-00014 University of Helsinki, Finland.

School of Plant Biology and Institute of Agriculture, Faculty of Natural and Agricultural Sciences, University of Western Australia, Perth, WA 6009, and Department of Agriculture, Locked Bag No. 4, Bentley Delivery Centre, Perth, WA 6983, Australia.

出版信息

Plant Dis. 2012 Oct;96(10):1430-1437. doi: 10.1094/PDIS-03-12-0268-RE.

Abstract

Sweetpotato (Ipomoea batatas) plants become infected with over 30 RNA or DNA viruses in different parts of the world but little is known about viruses infecting sweetpotato crops in Central America, the center of sweetpotato domestication. Small-RNA deep-sequencing (SRDS) analysis was used to detect viruses in sweetpotato in Honduras and Guatemala, which detected Sweet potato feathery mottle virus strain RC and Sweet potato virus C (Potyvirus spp.), Sweet potato chlorotic stunt virus strain WA (SPCSV-WA; Crinivirus sp.), Sweet potato leaf curl Georgia virus (Begomovirus sp.), and Sweet potato pakakuy virus strain B (synonym: Sweet potato badnavirus B). Results were confirmed by polymerase chain reaction and sequencing of the amplicons. Four viruses were detected in a sweetpotato sample from the Galapagos Islands. Serological assays available to two of the five viruses gave results consistent with those obtained by SRDS, and were negative for six additional sweetpotato viruses tested. Plants coinfected with SPCSV-WA and one to two other viruses displayed severe foliar symptoms of epinasty and leaf malformation, purpling, vein banding, or chlorosis. The results suggest that SRDS is suitable for use as a universal, robust, and reliable method for detection of plant viruses, and especially useful for determining virus infections in crops infected with a wide range of unrelated viruses.

摘要

甘薯(Ipomoea batatas)植株在世界不同地区会感染30多种RNA或DNA病毒,但对于感染中美洲甘薯作物(甘薯驯化中心)的病毒却知之甚少。利用小RNA深度测序(SRDS)分析来检测洪都拉斯和危地马拉甘薯中的病毒,检测到甘薯羽状斑驳病毒RC株系和甘薯病毒C(马铃薯Y病毒属)、甘薯褪绿矮化病毒WA株系(SPCSV-WA;毛形病毒属)、甘薯叶卷曲佐治亚病毒(菜豆金色花叶病毒属)以及甘薯帕卡库伊病毒B株系(同义词:甘薯杆状DNA病毒B)。通过聚合酶链反应和扩增子测序对结果进行了确认。在来自加拉帕戈斯群岛的一个甘薯样本中检测到了四种病毒。针对五种病毒中的两种的血清学检测结果与SRDS获得的结果一致,并且对另外六种检测的甘薯病毒呈阴性。同时感染SPCSV-WA和一到两种其他病毒的植株表现出严重的叶片症状,如叶片向下卷曲、叶片畸形、发紫、叶脉黄化或褪绿。结果表明,SRDS适合用作检测植物病毒的通用、强大且可靠的方法,尤其有助于确定感染多种不相关病毒的作物中的病毒感染情况。

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