利用聚合酶链反应灵敏检测香蕉束顶和蚕豆坏死黄病毒感染叶片、离体组织培养和毒蚜

A. Shamloul, A. Hadidi, M. Madkour, K. Makkouk
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引用次数: 13

摘要

根据香蕉束顶病毒(BBTV)和蚕豆坏死黄病毒(FBNYV)含有病毒推定复制酶基因的DNA成分1的核苷酸序列,构建了两种病毒的DNA引物。每种病毒的三对引物用于标准聚合酶链反应(PCR)或免疫捕获(IC) PCR扩增。从bbtv感染的香蕉叶、离体组织培养和毒蚜提取液中扩增出439、446和476 bp的DNA片段。从感染fbnyv的蚕豆植株和病毒载体提取液中扩增出487,931和1002 bp的DNA片段。扩增的DNA片段通过大小、核苷酸序列和(或)杂交分析进行鉴定。未感染的香蕉和蚕豆组织以及非病毒蚜虫的扩增提取物中没有病毒特异性DNA片段。pcr扩增的埃及人BBTV DNA组分1的主要部分(923个核苷酸)的核苷酸序列…
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Sensitive detection of banana bunchy top and faba bean necrotic yellows viruses from infected leaves, in vitro tissue cultures, and viruliferous aphids using polymerase chain reaction
DNA primers for banana bunchy top virus (BBTV) and for faba bean necrotic yellows virus (FBNYV) were constructed based on the nucleotide sequence of DNA component 1 of each virus that contains the viral putative replicase gene. Three pairs of primers for each virus were utilized for standard polymerase chain reaction (PCR) or immunocapture (IC) PCR amplification. DNA fragments of 439, 446, and 476 bp were amplified from extracts of BBTV-infected banana leaves, in vitro tissue culture, and viruliferous aphids. DNA fragments of 487, 931, and 1002 bp from extracts of FBNYV-infected faba bean plants and viruliferous vectors were also amplified. The amplified DNA fragments were identified by size, nucleotide sequence, and (or) hybridization analysis. Virus-specific DNA fragments were absent from amplified extracts of uninfected banana and faba bean tissues as well as from non-viruliferous aphids. The nucleotide sequence of the PCR-amplified major portion (923 nucleotides) of BBTV DNA component 1 of an Egyptian...
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