Detection and Genetic Fingerprint of Lethal Yellowing Disease Associated with Candidates Phytoplasma Palma in Egypt

Ahmed Ali, A. Elshazly, A. Metwaly, S. Darwish
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Abstract

The date palm (Phoenix dactylifera L.) is one of the oldest cultivated trees and is an important all-purpose tree. About 105 million date palms are planted in Africa and Central America, Spain and Italy, but in Egypt have 16 million. The date palm is one of the important crops that is considered a strategic crop, and the date palm suffers from diseases, the symptomatic tree streaking’s and yellowing to phytoplasma infection. The most important of which is phytoplasma disease, which is difficult to identify, this study using Molecular genetics has recently entered detection and genetic fingerprint of lethal yellowing disease, Polymerase chain reaction (PCR) assays using primer pairs designed for identification of phytoplasma using universal (R16mF2/R16mR1) primer 16Sr DNA sequences and specific nested (R16F2n/R16R2) a sensitive means of detecting this phytoplasma pathogen and a wide array of. The universal primer pair specifically for initiated amplification of among phytoplasma strains resulted in a DNA size of approximately 1500 bp in using gel electrophoresis. Nested PCR assays using the specific primer of phytoplasma in infected tissues resulted on a DNA of approximately 1200 bp. and Detection of LY-phytoplasma by the pathogen-specific primer pair LY1 (5ˋ-CAT ATT TTA TTT CCT TTG CAA TCTG-3ˋ), LY2 (5ˋ-TCG TTT TGA TGA TCT TTC ATT TGAC-3ˋ) designed for genomic DNA isolated from lethal yellow of windmill palm and electronics microscopy by transmission electron microscope At 70 kV, and Applied SEM Technology at sections of the infected leaves. This is examination of a phytoplasma associated with streak yellows on date palm in Egypt.
埃及与候选植物原体Palma相关的致死性黄化病的检测和遗传指纹图谱
枣椰树(Phoenix dactylifera L.)是最古老的人工栽培树种之一,是一种重要的多用途树种。在非洲、中美洲、西班牙和意大利种植了大约1.05亿棵椰枣树,但在埃及种植了1600万棵。枣椰树是我国重要的战略作物之一,枣椰树因受植物原体侵染而出现病状,出现有症状的树条病和黄化。其中最重要的是植物原体病,这是一种难以鉴定的致病性疾病,本研究利用分子遗传学方法最近进入了致病性黄化病的检测和遗传指纹,采用聚合酶链反应(PCR)方法设计了用于植物原体鉴定的引物对,采用通用(R16mF2/R16mR1)引物16Sr DNA序列和特异性嵌套(R16F2n/R16R2)一种灵敏的方法检测这种植物原体病原体和多种多样。凝胶电泳结果显示,用于植物原体菌株间起始扩增的通用引物对DNA大小约为1500 bp。利用感染组织中植原体的特异性引物进行巢式PCR分析,得到约1200 bp的DNA。利用设计的风棕毒黄基因组DNA特异引物LY1 (5 -CAT ATT TTA TTT CCT TTG CAA TCTG-3)、LY2 (5 -TCG TTT TGA TGA TCT TTC ATT TGAC-3)和70 kV透射电子显微镜对其进行检测,并应用扫描电镜技术对侵染叶片切片进行检测。这是对埃及枣椰树上与条纹黄有关的植物原体的检查。
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