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Molecular characterization of whole genomic RNA2 from Iranian isolates of Grapevine fanleaf virus.

机译:来自伊朗扇叶病毒伊朗分离株的完整基因组RNA2的分子表征。

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Grapevine fanleaf virus (GFLV) is the major causal agent of the grapevine degeneration disease. To characterize the genomic RNA2 segment from Iranian isolates of GFLV, leaf samples were collected from infected vineyards in different locations with a long history of vine cultivation. Four isolates were selected for cloning and sequencing on the basis of the restriction profiles of RT-PCR products. The sequencing data revealed that the RNA2 of the Iranian GFLV isolates were the shortest compared with that of all previously described GFLV isolates. The sizes were 3730 nucleotides (nt) for Shir-Amin and Urmia isolates and 3749 nt for Takestan and Bonab isolates (excluding the poly (A) tail), due to deletion events in both 5' and 3' non-coding regions. In the phylogenetic tree based on the full-length nucleotide sequences of GFLV RNA2, all the GFLV isolates clustered into two groups with the exception of the Hungarian isolate (GHu). The Iranian isolates grouped as a distinct cluster. Recombination analyses showed that GFLV-NW (Germany), GFLV-F13 (reference isolate), GFLV isolate Shir-Amin (Iran) and Arabis mosaic virus isolate Lv were recombinant isolates and one of their parents belonged to the same lineage as the Iranian isolates. These findings suggest that these isolates originated from a common ancestor.Digital Object Identifier http://dx.doi.org/10.1111/jph.12089
机译:葡萄扇叶病毒(GFLV)是葡萄变性疾病的主要病因。为了表征来自GFLV伊朗分离物的基因组RNA2片段,从葡萄树栽培历史悠久的不同位置的受感染葡萄园中收集了叶片样品。根据RT-PCR产物的限制性酶切图谱,选择了四种分离株进行克隆和测序。测序数据显示,与所有先前描述的GFLV分离株相比,伊朗GFLV分离株的RNA2最短。由于5'和3'非编码区的缺失事件,Shir-Amin和Urmia分离株的大小为3730核苷酸(nt),Takestan和Bonab分离株的大小为3749 nt(不包括poly(A)尾部)。在基于GFLV RNA2全长核苷酸序列的系统树中,除匈牙利分离株(GHu)外,所有GFLV分离株均分为两组。伊朗隔离株分为不同的簇。重组分析表明,GFLV-NW(德国),GFLV-F13(参考分离株),GFLV分离株Shir-Amin(伊朗)和Arabis花叶病毒分离株Lv是重组分离株,它们的父母之一与伊朗分离株属于同一血统。 。这些发现表明这些分离株起源于共同祖先。数字对象标识符http://dx.doi.org/10.1111/jph.12089

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