Bipartite geminivirus host adaptation determined cooperatively by coding and noncoding sequences of the genome

Citation
Itd. Petty et al., Bipartite geminivirus host adaptation determined cooperatively by coding and noncoding sequences of the genome, VIROLOGY, 277(2), 2000, pp. 429-438
Citations number
24
Categorie Soggetti
Microbiology
Journal title
VIROLOGY
ISSN journal
00426822 → ACNP
Volume
277
Issue
2
Year of publication
2000
Pages
429 - 438
Database
ISI
SICI code
0042-6822(20001125)277:2<429:BGHADC>2.0.ZU;2-A
Abstract
Bipartite geminiviruses are small, plant-infecting viruses with genomes com posed of circular, single-stranded DNA molecules, designated A and B. Altho ugh they are closely related genetically, individual bipartite geminiviruse s frequently exhibit host-specific adaptation. Two such viruses are bean go lden mosaic virus (BGMV) and tomato golden mosaic virus (TGMV), which are w ell adapted to common bean (Phaseolus vulgaris) and Nicotiana benthamiana, respectively. In previous studies, partial host adaptation was conferred on BGMV-based or TGMV-based hybrid viruses by separately exchanging open read ing frames (ORFs) on DNA A or DNA B. Here we analyzed hybrid viruses in whi ch all of the ORFs on both DNAs were exchanged except for AL1, which encode s a protein with strictly virus-specific activity. These hybrid viruses exh ibited partial transfer of host-adapted phenotypes. In contrast, exchange o f noncoding regions (NCRs) upstream from the AR1 and BR1 ORFs did not confe r any host-specific gain of function on hybrid viruses. However, when the e xchangeable ORFs and NCRs from TGMV were combined in a single BGMV-based hy brid virus, complete transfer of TGMV-like adaptation to N. benthamiana was achieved. Interestingly, the reciprocal TGMV-based hybrid virus displayed only partial gain of function in bean. This may be, in part, the result of defective virus-specific interactions between TGMV and BGMV sequences prese nt in the hybrid, although a potential role in adaptation to bean for addit ional regions of the BGMV genome cannot be ruled out. (C) 2000 Academic Pre ss.