Ambrós S, Desvignes J C, Llácer G, Flores R
Instituto de Biología Molecular y Celular de Plantas (UPV-CSIC), Universidad Politécnica de Valencia, Spain.
J Gen Virol. 1995 Oct;76 ( Pt 10):2625-9. doi: 10.1099/0022-1317-76-10-2625.
The sequences of several cDNA clones of pear blister canker viroid (PBCVd) P1914T and P47A isolates have been determined. Seven out of eight P1914T clones analysed have a constant sequence which differs at six positions from that of the P2098T isolate reported previously. The remaining P1914T clone (8) has a single nucleotide substitution. The same six changes have been also observed in most of the ten P47A clones sequenced. However, some P47A clones show additional variability in positions on both strands of the central conserved region (CCR) and in another conserved sequence at the left-terminal region. This is the first report of a change affecting the upper strand of a viroid CCR. Reasons why such a change is tolerated are discussed. Infectivity bioassays have demonstrated that PBCVd is the causal agent of PBC disease.
已确定梨疱溃疡类病毒(PBCVd)P1914T和P47A分离株的几个cDNA克隆的序列。在分析的8个P1914T克隆中,有7个具有恒定序列,该序列与先前报道的P2098T分离株在6个位置上不同。其余的P1914T克隆(8)有一个单核苷酸取代。在测序的10个P47A克隆中的大多数中也观察到了相同的6个变化。然而,一些P47A克隆在中央保守区(CCR)的两条链上的位置以及左末端区域的另一个保守序列中表现出额外的变异性。这是关于影响类病毒CCR上链的变化的首次报道。讨论了这种变化被容忍的原因。感染性生物测定表明PBCVd是梨疱溃疡病的病原体。