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Complementary (c)DNA clones corresponding to the full‐length genome of T36CA (a Californian isolate of  Citrus tristeza virus  with the T36 genotype), which shares 99.1% identity with that of T36FL (a T36 isolate from Florida), were made into a vector system to express the green fluorescent protein (GFP). Agroinfiltration of two prototype T36CA‐based vectors (pT36CA) to  Nicotiana benthamiana  plants resulted in local but not systemic GFP expression/viral infection. This contrasted with agroinfiltration of the T36FL‐based vector (pT36FL), which resulted in both local and systemic GFP expression/viral infection. A prototype T36CA systemically infected RNA silencing‐defective  N. benthamiana  lines, demonstrating that a genetic basis for its defective systemic infection was RNA silencing. We evaluated the in planta bioactivity of chimeric pT36CA‐pT36FL constructs and the results suggested that nucleotide variants in several open reading frames of the prototype T36CA could be responsible for its defective systemic infection. A single amino acid substitution in each of two silencing suppressors, p20 (S107G) and p25 (G36D), of prototype T36CA facilitated its systemic infectivity in  N. benthamiana  (albeit with reduced titre relative to that of T36FL) but not in  Citrus macrophylla  plants. Enhanced virus accumulation and, remarkably, robust systemic infection of T36CA in  N. benthamiana  and  C. macrophylla  plants, respectively, required two additional amino acid substitutions engineered in p65 (N118S and S158L), a putative closterovirus movement protein. The availability of pT36CA provides a unique opportunity for comparative analysis to identify viral coding and noncoding nucleotides or sequences involved in functions that are vital for in planta infection.

molecular plant pathology

Comparative analysis identifies amino acids critical for citrus tristeza virus (T36CA) encoded proteins involved in suppression of RNA silencing and differential systemic infection in two plant species