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Mutations in the P3 Protein of Soybean mosaic virus G2 Isolates Determine Virulence on Rsv4-Genotype Soybean

机译:大豆病毒G2分离株P3蛋白中的突变决定了RSV4-基因型大豆的毒力

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摘要

Two Soybean mosaic virus (SMV) G2 isolates, L and L-RB, sharing high-sequence similarly but differing in ability to break Rsv4-mediated resistance in soybean, were investigated. Infectious clones corresponding to these two isolates and their chimeric clones resulting from swapping different regions of genomic cDNA between L and L-RB were constructed. Only L-RB or chimeras containing the middle fragment of L-RB cDNA showed virulence on Rsv4-genotype soybean. Sequence comparison analysis revealed that the middle genomic region of L and L-RB encodes four different amino acids. Point mutagenesis demonstrated that a single amino acid substitution (Q1033K) in the P3 protein determined virulence toward Rsv4 resistance. In addition, six new SMV Rsv4 resistance-breaking isolates, variants of the second passage on Williams 82 infected with the chimeras or mutants noninfectious on soybean carrying Rsv4, were obtained. Sequencing data indicated that these new isolates contain either the Q1033K mutation or a new substitution (G1054R) in P3. Site-directed mutagenesis confirmed the virulence role of the G1054R mutation on Rsv4-genotype soybean. Taken together, these data suggest that P3 of the SMV G2 strain is an avirulent determinant for Rsv4 and one single nucleotide mutation in P3 may be sufficient to compromise its elicitor function.
机译:研究了两种大豆叶病毒(SMV)G2分离物,L和L-RB,同样分享高序列,但在大豆中破坏RSV4介导的抗性的能力不同。构建了对应于这两种分离株的传染性克隆及其通过在L和L-Rb之间交换不同区域CDNA的不同区域而导致的嵌合克隆。含有L-RB cDNA的中间片段的L-RB或嵌合体在RSV4基因型大豆上显示出毒力。序列比较分析显示L和L-Rb的中间基因组区域编码四种不同的氨基酸。点诱变证明,P3蛋白中的单个氨基酸取代(Q1033K)确定了对RSV4电阻的毒力。此外,获得了六个新的SMV RSV4阻力分离株,获得了威廉姆斯82上的第二通道的变体,感染了嵌合体或突变体载有RSV4的无排感。测序数据表明,这些新的隔离株包含Q1033K突变或P3中的新替换(G1054R)。定向诱变的诱变证实了G1054R突变对RSV4-基因型大豆的毒力作用。总之,这些数据表明SMV G2菌株的P3是RSV4的无毒决定因素,P3中的一个单一核苷酸突变可能足以损害其Elicitor功能。

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