首页> 外文期刊>Journal of Phytopathology >Detection and Characterization of Phytoplasma and Sugarcane Yellow Leaf Virus Associated with Leaf Yellowing of Sugarcane
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Detection and Characterization of Phytoplasma and Sugarcane Yellow Leaf Virus Associated with Leaf Yellowing of Sugarcane

机译:与甘蔗叶黄有关的植原体和甘蔗黄叶病毒的检测与鉴定

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Leaves from sugarcane were collected from Egyptian plantation fields and tested for phytoplasma (Sugarcane yellows phytoplasma, SCYP) and Sugarcane yellow leaf virus (SCYLV) using nested PCR (with different primers) and RT-PCR, respectively. These results showed significant differences in the amplification of the PCR assays. The primer MLO-X/MLO-Y, which amplified the 16S-23S rDNA spacer region, was the most precise to detect the phytoplasma in sugarcane plants. Sequencing and restriction fragment length polymorphism analysis revealed that all tested phytoplasmas belonged to the 16SrI (aster yellows phytoplasma) group, with the exception of cultivar G84-47 belonged to the 16SrXI (Rice yellow dwarf phytoplasma) group. Three Egyptian sugarcane cultivars were phytoplasma free. Phylogenetic analyses of 34 screened accessions of 16S ribosomal DNA gene sequences of Candidatus phytoplasma including the ones collected from Egypt used in this study and those extracted from GenBank showed that they split into two distinct clusters. The phylogenetic analyses indicated that these phytoplasmas are closely related and share a common ancestor. All tested Egyptian sugarcane plants were infected by SCYLV with the exception of cultivar Phil-8013 which was virus free.
机译:从埃及人工林中收集甘蔗的叶片,并分别使用巢式PCR(使用不同引物)和RT-PCR进行了植原体(甘蔗黄植物原体,SCYP)和甘蔗黄叶病毒(SCYLV)的测试。这些结果显示出PCR测定法扩增的显着差异。扩增16S-23S rDNA间隔区的引物MLO-X / MLO-Y是检测甘蔗植物中植物质体的最精确方法。测序和限制性片段长度多态性分析表明,除G84-47品种属于16SrXI(水稻黄矮化植物)组外,所有测试的植物质均属于16SrI(紫黄植物质体)组。三个埃及甘蔗品种没有植物浆原体。系统发育分析植物假丝酵母的16S核糖体DNA基因序列的34个筛选部分,包括从本研究中使用的埃及收集的和从GenBank中提取的序列,显示它们分为两个不同的簇。系统发育分析表明,这些植原体密切相关并具有共同的祖先。除无病毒的Phil-8013品种外,所有测试的埃及甘蔗植物均受SCYLV感染。

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