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Distinct phylogenetic positions of Grapevine fanleaf virus isolates from Iran based on the movement protein gene

机译:基于运动蛋白基因的伊朗扇叶病毒分离株的不同系统发生位置

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In DAS-ELISAs of 86 grapevine samples from northwestern Iran, Grapevine fanleaf virus (GFLV) was detected in 18 samples. RT-PCR with two primer pairs (M2/M4 or M0/M4) corresponding to GFLV movement protein (MP) amplified the expected 854- and/or 1,489-bp fragment(s), respectively, from all ELISA-positive samples. Four smaller and three larger PCR products were cloned and sequenced, which revealed that the MP region of the isolates was 1,044 nucleotides (nt) long, corresponding to the GFLV MP. There were 83–86% nucleotide and 93–94% amino acid identities deduced between the MPs of the sequenced isolates. Nucleotide sequence identities of 81–87 and 75–79% were found between the MP regions of these isolates and that of previously published GFLV and Arabis mosaic virus (ArMV) strains/isolates, respectively. On a consensus parsimony tree based on the nucleotide sequences, isolates La208 and X300 remained distinct from previously reported GFLVs. This is the first molecular characterization of GFLV MP isolates from Iran.
机译:在来自伊朗西北部的86个葡萄样品的DAS-ELISA中,在18个样品中检测到葡萄扇叶病毒(GFLV)。使用对应于GFLV运动蛋白(MP)的两个引物对(M2 / M4或M0 / M4)进行RT-PCR,从所有ELISA阳性样品中分别扩增了预期的854-和/或1,489-bp片段。克隆了四个较小的和三个较大的PCR产物并进行了测序,结果表明,分离株的MP区域长1,044个核苷酸(nt),对应于GFLV MP。在测序的分离物的MP之间推断出83-86%的核苷酸同一性和93-94%的氨基酸同一性。在这些分离物的MP区域与先前发表的GFLV和Arabis花叶病毒(ArMV)菌株/分离物的MP区域之间发现的核苷酸序列同一性分别为81-87%和75-79%。在基于核苷酸序列的共有简约树上,分离株La208和X300与以前报道的GFLV仍然不同。这是来自伊朗的GFLV MP分离株的第一个分子表征。

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