用套式PCR方法检测和鉴定香蕉相关植原体

Saurma Mona Astrid Sibarani, T. Joko, S. Subandiyah
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引用次数: 4

摘要

已知在来自不同科的大约300种植物中,植原体与植物疾病有关。关于在印度尼西亚香蕉中存在植原体作为可导致香蕉疾病的病原体之一的信息从未报道过。本研究旨在通过嵌套PCR方法检测香蕉植原体的存在,并基于16S rRNA基因的序列分析鉴定获得的植原体。使用P1/P7初级对进行标准PCR,然后分别使用一对R16F2n/R16R2m23SR引物进行嵌套PCR,该引物可以在1600bp处连续扩增靶16S rRNA基因。BLAST分析结果表明,来自马来西亚塔西克马拉的manggala和来自班珠尔的Raja nangka两个香蕉细胞质核苷酸的系统发育分析结果与致死性枯萎病油棕植原体(Candidatus PhytopPlas asteris)具有更接近的遗传关系。该植原体属于16SrI-B组(紫荆黄)。
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Detection and Identification of Banana-associated Phytoplasma Using Nested-PCR Method
Phytoplasma is known to be associated with plant diseases in about 300 plant species from various families. Information on the presence of phytoplasma in bananas as one of the pathogens that can cause disease in bananas in Indonesia has never been reported. This research was conducted with the aim to detect the presence of banana phytoplasma by the nested-PCR method and to identify phytoplasma obtained based on the sequence analysis of the 16S rRNA gene. Standard PCR was carried out using P1/P7 primary pairs, followed by nested-PCR using a pair of R16F2n/R16R2m23SR primers separately that could amplify the target 16S rRNA genes in a row at 1600 bp. BLAST analysis shows that the results of phylogenetic analysis of banana phytoplasmic nucleotide cv. manggala from Tasikmalaya and cv. Raja nangka from Banjar has a genetic relationship that is closer to lethal wilt oil palm Phytoplasma (Candidatus Phytoplasma asteris). This phytoplasma belongs to the 16SrI-B group (aster yellows).
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审稿时长
12 weeks
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