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两种天然存在的大豆花叶病毒分离株的鉴定及分子特征分析,这两种分离株密切相关,但在克服Rsv4抗性的能力上存在差异。

Identification and molecular characterization of two naturally occurring Soybean mosaic virus isolates that are closely related but differ in their ability to overcome Rsv4 resistance.

作者信息

Gagarinova Alla G, Babu Mohan, Poysa Vaino, Hill John H, Wang Aiming

机构信息

Southern Crop Protection and Food Research Centre, Agriculture and Agri-Food Canada, 1391 Sandford Street, London, Ontario, Canada N5V 4T3.

出版信息

Virus Res. 2008 Dec;138(1-2):50-6. doi: 10.1016/j.virusres.2008.08.010. Epub 2008 Sep 30.

DOI:10.1016/j.virusres.2008.08.010
PMID:18793685
Abstract

A naturally occurring Rsv4 resistance-breaking isolate (L-RB) and a closely related non-resistance-breaking isolate (L) of Soybean mosaic virus (SMV) were identified in soybean fields in London, Ontario, Canada. The viral genomes of L and L-RB were completely sequenced. Each isolate has a 9585-nucleotide genome with a single open reading frame encoding a polyprotein of approximately 350 kDa. L-RB and L have a very high sequence similarity (99.6%) at both the nucleotide and amino acid levels. Phylogenetic analysis showed that the two isolates belong to the G2 pathotype. Pathogenicity predictions of all virus/soybean combinations, based on the phylogenetic profile, were confirmed by pathogenicity tests using L and L-RB isolates and soybeans carrying different resistance genes, with an exception that L-RB infected a soybean cultivar carrying Rsv4 resistance. The temporal and spatial proximity of L and L-RB and their high sequence similarity suggest L-RB was likely derived from the SMV-L quasispecies. Recombination analysis did not reveal the evidence of genetic recombination for the emergence of L-RB. Mutations introduced by virus-encoded RNA-dependent RNA polymerase during viral genome replication and selection pressure probably contributed to the occurrence of L-RB.

摘要

在加拿大安大略省伦敦市的大豆田中,鉴定出一种天然存在的大豆花叶病毒(SMV)的Rsv4抗性突破分离株(L-RB)和一种密切相关的非抗性突破分离株(L)。对L和L-RB的病毒基因组进行了全序列测定。每个分离株都有一个9585个核苷酸的基因组,带有一个单一开放阅读框,编码一个约350 kDa的多蛋白。L-RB和L在核苷酸和氨基酸水平上都有非常高的序列相似性(99.6%)。系统发育分析表明,这两个分离株属于G2致病型。基于系统发育图谱对所有病毒/大豆组合的致病性预测,通过使用L和L-RB分离株以及携带不同抗性基因的大豆进行致病性试验得到了证实,但有一个例外,即L-RB感染了携带Rsv4抗性的大豆品种。L和L-RB在时间和空间上的接近以及它们的高序列相似性表明,L-RB可能源自SMV-L准种。重组分析未发现L-RB出现的基因重组证据。病毒编码的RNA依赖性RNA聚合酶在病毒基因组复制过程中引入的突变和选择压力可能促成了L-RB的出现。

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