Characterization of Citrus Tristeza Virus Subgenomic RNAs in Infected Tissue

• Published in: Virology (New York, N.Y.) N.Y.), 1995-04, Vol.208 (2), p.576-582
• Main Authors: Hilf, Mark E., Karasev, Alexander V., Pappu, Hanumantha R., Gumpf, David J., Niblett, Charles L., Garnsey, Stephen M.
• Format: Article
• Language: English
• Subjects: adn; arn; citrus; Citrus - virology; clone; clones; closterovirus; Closterovirus - genetics; closteroviruses; dna; DNA Probes; infeccion; infection; Open Reading Frames - genetics; plant viruses; rna; RNA, Double-Stranded - analysis; RNA, Double-Stranded - genetics; RNA, Viral - analysis; RNA, Viral - genetics; Serial Passage; Virion - chemistry; virus de las plantas; virus des vegetaux
• ISSN: 0042-6822; 1096-0341
• DOI: 10.1006/viro.1995.1188

Citrus tristeza virus (CTV) specific RNAs extracted from infected citrus tissue were analyzed by Northern blot hybridization. RNAs were characterized by size and identified using cDNA probes specific to nine open reading frames (ORFs) identified by the analysis of sequence obtained from cDNA clones of the T36 isolate of CTV. Sequence specific cDNA probes identified the genomic RNA as well as subgenomic RNAs representing the p33, p65, p61, p27, p25, p18, p13, p20, and p23 ORFs in extracts of total or double-stranded RNA (dsRNA) isolated from infected tissue. A probe derived from the 3′ terminal ORF (p23) hybridized to each of these subgenomic RNAs, indicating that the RNAs are 3′ coterminal. The relative amounts of the different subgenomic RNAs varied widely. The RNAs for the p20 and p23 ORFs were the most abundant and surpassed the amount of the p25 or capsid protein specific subgenomic RNA. The number and sizes of the CTV subgenomic RNAs were the same in total RNA and dsRNA preparations. Propagation of T36 in seven different citrus hosts did not alter the pattern of subgenomic RNAs.