Vives María Carmen, Martín Susana, Ambrós Silvia, Renovell Agueda, Navarro Luis, Pina Jose Antonio, Moreno Pedro, Guerri José
Centro de Protección Vegetal y Biotecnología, Instituto Valenciano de Investigaciones Agrarias (IVIA), 46113 Moncada, Valencia, Spain.
Mol Plant Pathol. 2008 Nov;9(6):787-97. doi: 10.1111/j.1364-3703.2008.00501.x.
Citrus leaf blotch virus (CLBV), a member of the family Flexiviridae, has a ~9-kb single-stranded, positive-sense genomic RNA encapsidated by a 41-kDa coat protein. CLBV isolates are associated with symptom production in citrus including leaf blotching of Dweet tangor and stem pitting in Etrog citron (Dweet mottle disease), and some isolates are associated with bud union crease on trifoliate rootstocks, but Koch's postulates for this virus were not fulfilled. A full-genome cDNA of CLBV isolate SRA-153, which induces bud union crease, was placed under the T7 promoter (clone T7-CLBV), or between the 35S promoter and the Nos-t terminator, with or without a ribozyme sequence downstream of the CLBV sequence (clones 35SRbz-CLBV and 35S-CLBV). RNA transcripts from T7-CLBV failed to infect Etrog citron and Nicotiana occidentalis and N. benthamiana plants, whereas agro-inoculation with binary vectors carrying 35SRbz-CLBV or 35S-CLBV, and the p19 silencing suppressor, caused systemic infection and production of normal CLBV virions. Virus accumulation was similar in citron plants directly agro-infiltrated, or mechanically inoculated with wild-type or 35SRbz-CLBV-derived virions from Nicotiana, and the three sources incited the symptoms characteristic of Dweet mottle disease, but not bud union crease. Our results show that (1) virions derived from an infectious clone show the same replication, movement and pathogenicity characteristics as the wild-type CLBV; (2) CLBV is the causal agent of Dweet mottle disease but not of the bud union crease syndrome; and (3) for the first time an RNA virus could be successfully agro-inoculated on citrus plants. This infectious clone may become a useful viral vector for citrus genomic studies.
柑橘叶斑病毒(CLBV)是柔线病毒科的成员,其约9kb的单链正义基因组RNA由一种41kDa的外壳蛋白包裹。CLBV分离株与柑橘的症状产生有关,包括Dweet橘柚的叶片斑点和Etrog枸橼的茎陷点(Dweet斑驳病),一些分离株与三叶砧木上的芽接痕有关,但该病毒的柯赫氏法则未得到满足。诱导芽接痕的CLBV分离株SRA - 153的全基因组cDNA被置于T7启动子下(克隆T7 - CLBV),或置于35S启动子和Nos - t终止子之间,CLBV序列下游有或没有核酶序列(克隆35SRbz - CLBV和35S - CLBV)。来自T7 - CLBV的RNA转录本未能感染Etrog枸橼、西方烟草和本氏烟草植株,而用携带35SRbz - CLBV或35S - CLBV以及p19沉默抑制子的二元载体进行农杆菌接种,会导致系统感染并产生正常的CLBV病毒粒子。在直接进行农杆菌浸润或用来自烟草的野生型或35SRbz - CLBV衍生的病毒粒子进行机械接种的枸橼植株中,病毒积累情况相似,并且这三种来源引发了Dweet斑驳病的特征性症状,但没有引发芽接痕。我们的结果表明:(1)来自感染性克隆的病毒粒子表现出与野生型CLBV相同的复制、移动和致病特性;(2)CLBV是Dweet斑驳病的病原体,但不是芽接痕综合征的病原体;(3)首次成功地在柑橘植株上进行了RNA病毒的农杆菌接种。这种感染性克隆可能成为柑橘基因组研究中有用的病毒载体。