COMPARATIVE SUSCEPTIBILITY OF TRANSGENIC TOBACCO PLANTS AND PROTOPLASTS EXPRESSING THE COAT PROTEIN GENE OF CUCUMBER MOSAIC-VIRUS TO INFECTION WITH VIRIONS AND RNA

Citation
T. Okuno et al., COMPARATIVE SUSCEPTIBILITY OF TRANSGENIC TOBACCO PLANTS AND PROTOPLASTS EXPRESSING THE COAT PROTEIN GENE OF CUCUMBER MOSAIC-VIRUS TO INFECTION WITH VIRIONS AND RNA, Phytopathology, 83(5), 1993, pp. 542-547
Citations number
39
Categorie Soggetti
Plant Sciences
Journal title
ISSN journal
0031949X
Volume
83
Issue
5
Year of publication
1993
Pages
542 - 547
Database
ISI
SICI code
0031-949X(1993)83:5<542:CSOTTP>2.0.ZU;2-4
Abstract
A cDNA clone encoding the coat protein (CP) gene of cucumber mosaic vi rus (CMV, Y strain), linked to the caulifiower mosaic virus (CaMV) 35S transcript promoter, was introduced into tobacco tissues by either el ectroporation or Agrobacterium-mediated gene transfer. The inoculated and upper systemic leaves of transgenic tobacco plants expressing the CMV-CP gene were highly protected from infection with CMV, even when t he concentration of CMV-virion inoculum was 100 mug/ml. Inoculated lea ves, however, often showed greater susceptibility to CMV RNA than to C MV virions. Protoplasts isolated from these transgenic plants also wer e protected from infection when inoculated with CMV virions but were a s susceptible as the control protoplasts when inoculated with CMV RNA and unrelated viruses, such as tobacco mosaic virus and brome mosaic v irus (BMV), and their respective RNAs. The results suggest protection from virus infection in transgenic protoplasts expressing the CMV-CP g ene was specific to infection by CMV virions, and interference with an early event in the infection process, such as uncoating virus particl es, is probably involved in the resistance of transgenic tobacco plant s expressing the CMV-CP gene. The observed resistance against CMV RNA in whole plants suggests virus replication may occur in primary infect ed cells, but the initiation of the replication process in adjacent ce lls may be inhibited by the resident CMV-CP gene if RNA encapsidation or binding to the CP is required for cell-to-cell and long-distance tr ansport.