Khasa Ekta, Taloh Aido, Prabha T, Rao G P
Division of Plant Pathology, Indian Agricultural Research Institute, Pusa Campus, New Delhi, 110012, India.
Directorate of Floricultural Research College of Agriculture, MPKV, Shivajinagar, Pune, 411005, India.
3 Biotech. 2016 Dec;6(2):237. doi: 10.1007/s13205-016-0558-8. Epub 2016 Nov 11.
Suspected phytoplasma symptoms of little leaf, yellowing, chlorosis, phyllody, witches' broom, and stunting were observed on ten different ornamental plant species at New Delhi, Andhra Pradesh, Haryana, Bengaluru, and Pune, India, during March to July 2016. To investigate the possibility of phytoplasma etiology, PCR assays were performed using universal primer pairs (P1/P7 followed by 3Far/3Rev) specific to the phytoplasma 16Sr RNA gene. First round PCR amplification with primer pair P1/P7 did not yield expected 1.8 kb product of 16S rRNA region from any of the 17 symptomatic samples. However, 1.3 Kb amplicons were observed in nested PCR assays with 3Far/3Rev primer pair in symptomatic leaf samples of Hibiscus rosa-sinensis L. (Pune isolate), Saponaria officinalis L. (Pune isolate), and Allamanda cathartica L. (Delhi isolate). No amplifications were observed in any of the other tested symptomatic and non-symptomatic plant samples either in first round or second round of nested PCR assays with phytoplasma specific primer pairs. Pairwise sequence comparison of 16S rDNA sequences of the five positive phytoplasma strains of A. catharica, H. rosa-sinensis, and S. officinalis in the present study revealed 99-100% sequence identities with strains of 'clover proliferation' (16SrVI) group. Phylogenetic and virtual RFLP analysis of 16S rDNA sequences of the five identified phytoplasma strains belonging to three ornamental species further confirmed their clustering and grouping with member strains of 'clover proliferation' subgroup D. This is the first record of the phytoplasma association of 'clover proliferation' subgroup D with H. rosa-sinensis, S. officinalis, and A. cathartica in the world.
2016年3月至7月期间,在印度新德里、安得拉邦、哈里亚纳邦、班加罗尔和浦那,在10种不同的观赏植物品种上观察到疑似植原体症状,如小叶、黄化、褪绿、叶变花、扫帚状丛生和生长受阻。为了调查植原体病因的可能性,使用针对植原体16Sr RNA基因的通用引物对(P1/P7,随后是3Far/3Rev)进行了PCR检测。第一轮使用引物对P1/P7的PCR扩增未从17个有症状的样本中得到预期的16S rRNA区域1.8 kb产物。然而,在对芙蓉(浦那分离株)、肥皂草(浦那分离株)和黄蝉(德里分离株)的有症状叶片样本进行的嵌套PCR检测中,使用3Far/3Rev引物对观察到了1.3 Kb扩增子。在第一轮或第二轮使用植原体特异性引物对的嵌套PCR检测中,在任何其他测试的有症状和无症状植物样本中均未观察到扩增。本研究中对黄蝉、芙蓉和肥皂草的五个阳性植原体菌株的16S rDNA序列进行的成对序列比较显示,与“三叶草增殖”(16SrVI)组的菌株具有99 - 100%的序列同一性。对属于三个观赏物种的五个已鉴定植原体菌株的16S rDNA序列进行的系统发育和虚拟RFLP分析进一步证实了它们与“三叶草增殖”亚组D的成员菌株聚类和分组。这是世界上首次记录“三叶草增殖”亚组D的植原体与芙蓉、肥皂草和黄蝉相关联。