Analysis of Soybean mosaic virus genetic diversity in Iran allows the characterization of a new mutation resulting in overcoming Rsv4-resistance

被引:23
作者
Ahangaran, Akbar [1 ]
Habibi, Mina Koohi [1 ]
Mohammadi, Gholam-Hossein Mosahebi [1 ]
Winter, Stephan [2 ]
Garcia-Arenal, Fernando [3 ,4 ]
机构
[1] Univ Tehran, Univ Coll Agr & Nat Resources, Dept Plant Protect, Karaj, Iran
[2] Deutsch Sammlung Mikroorganism Zellkultur GmbH, German Collect Microorganisms & Cell Cultures, Braunschweig, Germany
[3] Univ Politecn Madrid, Ctr Biotecnol & Genom Plantas UPM INIA, Madrid, Spain
[4] Univ Politecn Madrid, ETSI Agronomos, Madrid, Spain
关键词
RNA VIRUSES; HYPERSENSITIVE RESPONSE; P3; PROTEIN; CONFERRING RESISTANCE; MOLECULAR EVOLUTION; RECOMBINATION; VIRULENCE; STRAINS; RATES; POPULATION;
D O I
10.1099/vir.0.055434-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The genetic variation and population structure of Soybean mosaic virus (SMV) in Iran was analysed through the characterization of a set of isolates collected in the soybean-growing provinces of Iran. The partial nucleotide sequence of these isolates showed a single, undifferentiated population with low genetic diversity, highly differentiated from other SMV world populations. These traits are compatible with a population bottleneck associated with the recent introduction of SMV in Iran. Phylogenetic analyses suggest that SMV was introduced into Iran from East Asia, with at least three introduction events. The limited genetic diversification of SMV in Iran may be explained by strong negative selection in most viral genes eliminating the majority of mutations, together with recombination purging deleterious mutations. The pathogenicity of Iranian SMV isolates was typified on a set of soybean differential lines either susceptible or carrying different resistance genes or alleles to SMV. Two pathotypes were distinguished according to the ability to overcome Rsv4 resistance in line V94-5152. Amino acid sequence comparisons of virulent and avirulent isolates on V94-5152 (Rsv4), plus site-directed mutagenesis in a biologically active cDNA clone, identified mutation S1 053N in the P3 protein as the determinant for virulence on V94-5152. Codon 1053 was shown to be under positive selection, and S1 053N-determined Rsv4-virulence occurred in isolates with different genealogies. The V94-5152 (Rsv4)-virulence determinant in Iranian isolates maps into a different amino acid position in the P3 protein than those previously reported, indicating different evolutionary pathways towards resistance breaking that might be conditioned by sequence context.
引用
收藏
页码:2557 / 2568
页数:12
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