Abstract:
:A full-length cDNA of cucurbit aphid-borne yellows virus (CABYV) has been constructed and expressed either as an in vitro transcript, under control of a bacteriophage T7 RNA polymerase promoter, or in vivo, under control of the cauliflower mosaic virus 35S promoter in an agroinfection vector. The biological activity of the cloned cDNA was demonstrated by the ability of its in vitro transcript to replicate in protoplasts and of the agroinfection vector to infect agroinoculated plants. Virus in the agroinfected plants cold be transmitted by the aphid vectors Myzus persicae and Aphis gossypii. The specificity of luteovirus RNA packaging was investigated by replacing (1) the CABYV coat protein gene (and the overlapping ORF5) by the corresponding region of potato leafroll luteovirus or (2) the CABYV readthrough domain by the readthrough domain of beet western yellows luteovirus. The resulting chimeric transcripts replicated in protoplasts and produced virions.
journal_name
Virologyjournal_title
Virologyauthors
Prüfer D,Wipf-Scheibel C,Richards K,Guilley H,Lecoq H,Jonard Gdoi
10.1006/viro.1995.9945subject
Has Abstractpub_date
1995-12-01 00:00:00pages
150-8issue
1eissn
0042-6822issn
1096-0341pii
S0042-6822(85)79945-Xjournal_volume
214pub_type
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