Quan S, Nelson R S, Deom C M
Department of Plant Pathology, Plant Sciences Building, The University of Georgia, Athens, GA 30602-7274, USA.
Arch Virol. 2008;153(8):1505-16. doi: 10.1007/s00705-008-0137-3. Epub 2008 Jul 6.
The type strain of cowpea chlorotic mottle virus (CCMV-T) induces a local and systemic infection in California Blackeye cowpea (Vigna unguiculata (L.) Walp. subs. unguiculata cv. California Blackeye), but accumulates to low levels in inoculated leaves and fails to accumulate systemically in the cowpea plant introduction (PI) 186465. CCMV-R, a mutant strain derived from CCMV-T, accumulates to higher levels than CCMV-T in inoculated leaves and systemically infects PI 186465 plants. The phenotypic determinant of CCMV-R was previously mapped to viral RNA1, but the location of the determinant within RNA1 was not identified. Pseudorecombinants generated from genomic cDNA clones of CCMV-T and CCMV-R indicated that the phenotypic differences on PI 186465 were independent of replication. Through the use of chimeric RNA1 cDNA clones containing portions of CCMV-T and CCMV-R and site-directed mutagenesis, two nucleotides, 299 (amino acid residue 77) and 951 (amino acid residue 294), were identified as being independently critical for the local and systemic accumulation patterns of CCMV-R in PI 186465 plants. A second independently derived CCMV-R-like mutant, identified nucleotide 216 (amino acid residue 49) as being critical for induction of the CCMV-R infection phenotype. Amino acid residues 49, 77, and 294 are within the methytransferase domain of the CCMV 1a protein, suggesting that the methytransferase domain has a role in cell-to-cell and systemic accumulation of the virus that is independent of replication.
豇豆褪绿斑驳病毒(CCMV-T)的模式菌株在加利福尼亚黑眼豇豆(Vigna unguiculata (L.) Walp. subs. unguiculata cv. California Blackeye)中引发局部和系统感染,但在接种叶片中积累水平较低,且在豇豆植株引进种(PI)186465中未能系统积累。CCMV-R是从CCMV-T衍生而来的突变菌株,在接种叶片中积累水平高于CCMV-T,并能系统感染PI 186465植株。CCMV-R的表型决定因素先前已定位到病毒RNA1,但RNA1内决定因素的位置尚未确定。由CCMV-T和CCMV-R的基因组cDNA克隆产生的假重组体表明,PI 186465上的表型差异与复制无关。通过使用包含CCMV-T和CCMV-R部分的嵌合RNA1 cDNA克隆以及定点诱变,确定了两个核苷酸299(氨基酸残基77)和951(氨基酸残基294)对CCMV-R在PI 186465植株中的局部和系统积累模式独立起关键作用。另一个独立衍生的类CCMV-R突变体确定核苷酸216(氨基酸残基49)对CCMV-R感染表型的诱导起关键作用。氨基酸残基49、77和294位于CCMV 1a蛋白的甲基转移酶结构域内,表明甲基转移酶结构域在病毒的细胞间和系统积累中具有独立于复制的作用。