Santosh Watpade, Baswaraj Raigond, P D Thakur, Anil Handa, K K Pramanick, Y P Sharma, Manica Tomar
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引用次数: 16
摘要
苹果褪绿叶斑病病毒;毛状病毒(Betaflexiviridae genus Trichovirus)是侵染苹果(Malus × domestica Borkh.)的重要经济潜伏病毒之一。采用逆转录聚合酶链反应(RT-PCR)方法扩增ACLSV外壳蛋白基因。在使用的5个引物集合中,两个引物集合(1F1R和1F2R)扩增了预期大小的片段(432 bp)。琼脂糖凝胶上可见的产品是用从苹果叶中提取的模板生产的。利用引物集1F - 1R从苹果叶片中扩增出432 bp的序列片段,进一步验证了结果。与已发表的序列比较表明,该分离物与苹果ACLSV分离物对应区域的同源性高达91%。选取的引物对(1F1R)进一步筛选了来自印度喜马偕尔邦苹果产区的42株优质母本,其中17株无ACLSV。利用苹果线粒体mRNA中的NAD5基因作为内控,降低了常规RT-PCR检测可能出现假阴性结果的风险。
Molecular Detection of Latent Apple chlorotic leaf spot virus in Elite Mother Plants of Apple.
Apple chlorotic leaf spot virus (ACLSV; family Betaflexiviridae genus Trichovirus) is one of the economically important latent virus infecting apple (Malus × domestica Borkh.). Reverse transcriptase polymerase chain reaction (RT-PCR) procedures were used to amplify coat protein gene of ACLSV. Among 5 primer sets used, two primer sets (1F1R and 1F2R) amplified fragments of expected size (432 bp). Products visible on agarose gel were produced using templates extracted from apple leaves. The results were further validated by sequencing fragment of 432 bp which was amplified from leaf of apple by using primer set 1F 1R. Comparisons with published sequences indicated that the isolate have very high 91 % identity values to the corresponding region of ACLSV isolate from apple. Selected primer pair (1F1R) was further used for screening 42 elite mother plants collected from apple growing areas of Himachal Pradesh, India, where in 17 were found free from ACLSV. Use of NAD5 gene in mitochondrial mRNA of the apple as an internal control, reduced the risk of false negative results that may occur with routine RT-PCR assays.