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Efficient inoculation with CaMV 35 S promoter-driven DNA clones of the tobravirus PEBV
S A MacFarlane1, D Gilmer, J W Davies
1Department of Virus Research, John Innes Institute, John Innes Centre for Plant Science Research, Norwich, United Kingdom.
Virology
|April 1, 1992
Abstract:
Clones have been constructed containing full-length cDNA copies of PEBV RNA1 and RNA2, flanked by the CaMV 35 S RNA promoter and the nopaline synthase terminator. The clones are infectious when inoculated onto Nicotiana benthamiana plants. Both the viral RNAs and the virus particles were identified in infected plants.
