首页> 外文期刊>Journal of Plant Biochemistry and Biotechnology >Molecular Variability in the Replicase Gene of Viruses Causing Tomato Leaf Curl Disease in India
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Molecular Variability in the Replicase Gene of Viruses Causing Tomato Leaf Curl Disease in India

机译:在印度引起番茄卷毛病的病毒复制酶基因中的分子变异性

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Tomato Leaf Curl Virus (ToLCV)-infected samples collected from four different ecological zones of India: Northern zone, New-Delhi (IARI) [ToLCNDV-IARI]; Central zone, Jabalpur [ToLCV-Jb], Raipur [ToLCV-Rp] and Southern zone, Dharwad [ToLCV-Dh] were maintained by whitefly transmission into tomato cv Pusa Early Dwarf. Replicase gene coding for replication initiator protein (Rep) was amplified by PCR using gene specific primers, yielding an amplicon of 1086 bp for all the isolates. Sequence analysis ofthe rep amplicons of all the Indian isolates of ToLCV causing the disease clearly shows the presence of two subgroups irrespective of their geographical evolution. Isolates belonging to subgroup I comprising of tomato leaf curl virus-New Delhi (ToLCV-NDe) having bipartite genome are conserved within themselves and showed 94-95% nucleotide sequence homology. Second subgroup comprising of tomato leaf curl virus-Bangalore (ToLCBV) having monopartite genome and conserved among themselves, but showed only 73-75% homology with the subgroup I. In phylogenetic tree analysis, ToLCV-NDe appeared in a different cluster than ToLCV-Ban. All the four isolates used in this study fall in ToLCV-NDe group based on their replicase gene sequences. The specificity determinant located at N terminal suggests ToLCV-NDe and ToLCV-Rp as mild isolates.
机译:番茄叶卷曲病毒(ToLCV)感染的样本来自印度的四个不同生态区域:北部区域,新德里(IARI)[ToLCNDV-IARI];贾巴尔普尔(Jabalpur)的中部地区[ToLCV-Jb],赖布尔(Raipur)[ToLCV-Rp]和达瓦尔(Dharwad)南部地区[ToLCV-Dh]通过将粉虱传播到番茄Cusa Pusa Early Dwarf中来维持。使用基因特异性引物通过PCR扩增编码复制起始蛋白(Rep)的复制酶基因,所有分离物的扩增子均为1086 bp。对印度所有导致该病的ToLCV分离株的rep扩增子进行的序列分析清楚地表明,存在两个亚组,而与它们的地理进化无关。属于具有二分基因组的番茄叶片卷曲病毒-新德里(ToLCV-NDe)的第一亚组的分离物在其内部是保守的,并显示出94-95%的核苷酸序列同源性。第二亚组由番茄叶片卷曲病毒-班加罗尔(ToLCBV)组成,具有单部分基因组并且彼此保守,但与I亚组仅显示73-75%的同源性。在系统树分析中,ToLCV-NDe与ToLCV-C的簇不同。禁止。根据其复制酶基因序列,本研究中使用的所有四种分离株均属于ToLCV-NDe组。位于N末端的特异性决定子表明ToLCV-NDe和ToLCV-Rp为轻度分离株。

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