Replicase-Mediated Resistance to Cucumber Mosaic Virus in Transgenic Plants Involves Suppression of Both Virus Replication in the Inoculated Leaves and Long-Distance Movement

Tobacco plants transformed with a gene encoding a truncated cucumber mosaic virus (CMV) 2a replicase protein are resistant to systemic CMV disease. Experiments using protoplasts derived from plants of two R 2-generation CMV-resistant transgenic plant lines (lines R 2-2 and R 2-5) showed that resista...

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Published inVirology (New York, N.Y.) Vol. 199; no. 2; pp. 439 - 447
Main Authors Carr, John P., Gal-On, Amit, Palukaitis, Peter, Zaitlin, Milton
Format Journal Article
LanguageEnglish
Published San Diego, CA Elsevier Inc 01.03.1994
Elsevier
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Summary:Tobacco plants transformed with a gene encoding a truncated cucumber mosaic virus (CMV) 2a replicase protein are resistant to systemic CMV disease. Experiments using protoplasts derived from plants of two R 2-generation CMV-resistant transgenic plant lines (lines R 2-2 and R 2-5) showed that resistance operates at the single cell level. Low levels of CMV-specific RNAs were detected in CMV-inoculated protoplasts obtained from both R 2-2 and R 2-5 plants indicating that resistance is due at least in large part to a marked but incomplete suppression of virus replication. Leaves of immature plants belonging to line R 2-2 occasionally exhibited local chlorosis when inoculated with high concentrations of CMV. Areas of local chlorosis were sites of low but detectable levels of CMV RNA, CMV virions, and CMV replicase activity, but did not act as foci for subsequent systemic disease. An antiserum raised against the CMV 2a replicase protein overexpressed in Escherichia coli was used to detect the presence of trace amounts of the truncated CMV 2a replicase protein in CMV-resistant transgenic tobacco plants. It was concluded that expression of the transgene, potentially as protein, engenders resistance primarily by suppressing virus replication but may also, to a lesser extent, do so by inhibiting systemic movement of the virus.
Bibliography:9509388
H20
ObjectType-Article-2
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ISSN:0042-6822
1096-0341
DOI:10.1006/viro.1994.1142