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Molecular Detection and Characterization of Little Leaf Disease in Brinjal

机译:茄子小叶病的分子检测与表征

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A nested Polymerase Chain Reaction (PCR) was optimised to detect the phytoplasma pathogen of brinjal showing little leaf symptoms. The second round primers amplicon was then cloned with pGEMT vector and fully sequenced. A 1200 bp DNA fragment encodingthe portion from 16S rRNA gene of brinjal phytoplasma consistently amplified by universal primers and 890 bp from second round specific primers. The amplicon was cloned and sequenced. Nucleotide analyses of the fragment (GQ184436) showed that the gene was closely related to members of candidates phytoplasma. The sequence identity similarity with members of the clover proliferation group (16Sr VI) was >99%, while the sequence identity with members of other groups (16Sr VI Elm yellows group) showed 97-98% similarity. On the basis of sequence identity and phylogenetic relationship studies, it was concluded that the phytoplasma infecting brinjal in Tamil Nadu, India belonged to the clover proliferation group.
机译:优化了嵌套式聚合酶链反应(PCR),以检测显示很少叶片症状的茄子的植物质原体病原体。然后用pGEMT载体克隆第二轮引物扩增子并完全测序。 1200 bp DNA片段编码了茄属植物质体16S rRNA基因的一部分,该片段通过通用引物不断扩增,而从第二轮特异性引物扩增出890 bp。扩增子被克隆并测序。对该片段(GQ184436)的核苷酸分析表明,该基因与候选植物质体的成员密切相关。与三叶草增殖组成员(16Sr VI)的序列同一性相似度> 99%,而与其他组成员(16Sr VI Elm yellows组)的序列同一性相似性为97-98%。根据序列同一性和系统发育关系研究,可以得出结论,印度泰米尔纳德邦的茄子属感染茄子属属于三叶草增殖群。

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