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孟加拉国、老挝、马来西亚、缅甸和越南与番茄卷叶病相关的双生病毒的分子特征分析

Molecular Characterization of Begomoviruses Associated with Leafcurl Diseases of Tomato in Bangladesh, Laos, Malaysia, Myanmar, and Vietnam.

作者信息

Green S K, Tsai W S, Shih S L, Black L L, Rezaian A, Rashid M H, Roff M M N, Myint Y Y, Hong L T A

机构信息

The Asian Vegetable Research and Development Center (AVRDC), Shanhua, Tainan 741, Taiwan, Rep of China.

Commonwealth Scientific and Industrial Research Organization, Adelaide, Australia.

出版信息

Plant Dis. 2001 Dec;85(12):1286. doi: 10.1094/PDIS.2001.85.12.1286A.

Abstract

Production of tomato (Lycopersicon esculentum) in Bangladesh, Malaysia, Myanmar, Vietnam, and Laos has been severely affected by yellow leaf curl disease. Tomato leaf samples were collected from symptomatic tomato plants from farmers' fields in the five countries from 1997 to 1999. DNA was extracted from all samples, four from Vietnam, two each from Malaysia, Laos, and Myanmar, and seven from Bangladesh. Virus DNA was amplified by polymerase chain reaction (PCR) using the begomovirus-specific degenerate primer pair PAL1v 1978/PAR1c 715(1), which amplifies the top part of DNA A. All samples gave the expected 1.4-kb PCR product. The PCR product of one sample per country was cloned and sequenced. Based on the sequences of the 1.4-kb DNA products amplified by the first primer pair, specific primers were designed to complete each of the DNA A sequences. Computer-assisted sequence comparisons were performed with begomovirus sequences available in the laboratory at the Asian Vegetable Research and Development Center, Shanhua, Tainan, and in the GenBank sequence database. The five DNA species resembled DNA A of begomoviruses. For the detection of DNA B two degenerate primer pairs were used, DNABLC1/DNABLV2 and DNABLC2/DNABLV2 (DNABLC1: 5'-GTVAATGGRGTDCACTTCTG-3', DNABLC2: 5'-RGTDCACTT CTGYARGATGC-3', DNABLV2: 5'-GAGTAGTAGTGBAKGTTGCA-3'), which were specifically designed to amplify DNA B of Asian tomato geminiviruses. Only the virus associated with yellow leaf curl of tomato in Bangladesh was found to contain a DNA B component, which was detected with the DNABLC1/DNABLV2 primer pair. The DNA A sequence derived from the virus associated with tomato yellow leaf curl from Myanmar (GenBank Accession No. AF206674) showed highest sequence identity (94%) with tomato yellow leaf curl virus from Thailand (GenBank Accession No. X63015), suggesting that it is a closely related strain of this virus. The other four viruses were distinct begomoviruses, because their sequences shared less than 90% identity with known begomoviruses of tomato or other crops. The sequence derived from the virus associated with tomato yellow leaf curl from Vietnam (GenBank Accession No. AF264063) showed highest sequence identity (82%) with the virus associated with chili leaf curl from Malaysia (GenBank Accession No. AF414287), whereas the virus associated with yellow leaf curl symptoms in tomato in Bangladesh (GenBank Accession No. AF188481) had the highest sequence identity (88%) with a tobacco geminivirus from Yunnan, China (GenBank Accession No. AF240675). The sequence derived from the virus associated with tomato yellow leaf curl from Laos (GenBank Accession No. AF195782) had the highest sequence identity (88%) with the tomato begomovirus from Malaysia (GenBank Accession No. AF327436). This report provides further evidence of the great genetic diversity of tomato-infecting begomoviruses in Asia. Reference: M. R. Rojas et al. Plant Dis. 77:340, 1993.

摘要

孟加拉国、马来西亚、缅甸、越南和老挝的番茄(Lycopersicon esculentum)生产受到黄化曲叶病的严重影响。1997年至1999年期间,从这五个国家农民田地中出现症状的番茄植株上采集了番茄叶片样本。从所有样本中提取DNA,其中越南4份,马来西亚、老挝和缅甸各2份,孟加拉国7份。使用双生病毒特异性简并引物对PAL1v 1978/PAR1c 715(1)通过聚合酶链反应(PCR)扩增病毒DNA,该引物对扩增DNA A的顶部区域。所有样本均产生预期的1.4 kb PCR产物。每个国家选取一个样本的PCR产物进行克隆和测序。根据由第一对引物扩增出的1.4 kb DNA产物的序列,设计特异性引物以完成每个DNA A序列。利用亚洲蔬菜研究与发展中心(位于台南善化)实验室和GenBank序列数据库中已有的双生病毒序列进行计算机辅助序列比较。这五种DNA种类类似于双生病毒的DNA A。为检测DNA B,使用了两对简并引物,即DNABLC1/DNABLV2和DNABLC2/DNABLV2(DNABLC1:5'-GTVAATGGRGTDCACTTCTG-3',DNABLC2:5'-RGTDCACTT CTGYARGATGC-3',DNABLV2:5'-GAGTAGTAGTGBAKGTTGCA-3'),它们是专门设计用于扩增亚洲番茄双生病毒的DNA B的。结果发现,只有与孟加拉国番茄黄化曲叶病相关的病毒含有DNA B成分,使用DNABLC1/DNABLV2引物对检测到了该成分。源自缅甸番茄黄化曲叶病相关病毒的DNA A序列(GenBank登录号AF206674)与泰国番茄黄化曲叶病毒(GenBank登录号X63015)的序列一致性最高(94%),表明它是该病毒的一个密切相关菌株。其他四种病毒是不同的双生病毒,因为它们的序列与已知的番茄或其他作物双生病毒的序列一致性低于90%。源自越南番茄黄化曲叶病相关病毒的序列(GenBank登录号AF264063)与马来西亚辣椒曲叶病相关病毒(GenBank登录号AF414287)的序列一致性最高(82%),而与孟加拉国番茄黄化曲叶症状相关的病毒(GenBank登录号AF188481)与中国云南的一种烟草双生病毒(GenBank登录号AF

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