Polymorphism of a specific region in gene p23 of Citrus tristeza virus allows discrimination between mild and severe isolates

• Published in: Archives of virology 2003-12, Vol.148 (12), p.2325-2340
• Main Authors: SAMBADE, A, LOPEZ, C, RUBIO, L, FLORES, R, GUERRI, J, MORENO, P
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Biological and medical sciences; Citrus - virology; Citrus fruits; Citrus tristeza virus; Closterovirus - classification; Closterovirus - genetics; Fundamental and applied biological sciences. Psychology; Genes, Viral; Human viral diseases; Infectious diseases; Medical sciences; Microbiology; Miscellaneous; Molecular Sequence Data; p23 gene; Phylogeny; Polymorphism; Polymorphism, Genetic; Proteins; Reverse Transcriptase Polymerase Chain Reaction; RNA-Binding Proteins - genetics; Viral diseases; Virology; Virulence; Viruses
• ISSN: 0304-8608; 1432-8798
• DOI: 10.1007/s00705-003-0191-9

The pathogenicity determinants of Citrus tristeza virus (CTV) are presently unknown, although transgenic Mexican limes over-expressing CTV p23, an RNA-binding protein involved in regulating the asymmetrical accumulation of viral RNA strands, display typical CTV symptoms. Here we compared the predominant sequence variants of gene p23 from 18 CTV isolates of different geographic origin and pathogenicity characteristics. Phylogenetic analysis of these sequences revealed three groups of isolates: i) mild, inducing only symptoms in lime and/or decline of citrus species grafted on sour orange rootstock, ii) severe, causing additionally stem pitting on sweet orange and/or grapefruit, and iii) an atypical group of isolates inciting variable symptoms. The sequences of the isolates located at the periphery of each group were recombinants. Pairwise comparisons of the predicted amino acid sequences showed that residues at positions 78-80 were characteristic of each group of isolates. Group-specific primers based on these differences allowed RT-PCR detection of each sequence type in dsRNA-rich preparations from infected tissues. While mild isolates contained only the sequence characteristic of this group, most severe isolates contained the sequences characteristic of their group, and additionally, sequences characteristic of the mild and/or the atypical groups, suggesting that the severe phenotype is associated with the presence of the severe and/or the atypical sequence types. This association can be exploited for quick detection of potentially damaging sequence variants and for monitoring cross protection.