Moreno Pedro, Ambrós Silvia, Albiach-Martí Maria R, Guerri José, Peña Leandro
Instituto Valenciano de Investigaciones Agrarias, Cra. Moncada-Náquera Km. 4.5, Moncada, 46113- Valencia, Spain.
Mol Plant Pathol. 2008 Mar;9(2):251-68. doi: 10.1111/j.1364-3703.2007.00455.x.
Citrus tristeza virus (CTV) (genus Closterovirus, family Closteroviridae) is the causal agent of devastating epidemics that changed the course of the citrus industry. Adapted to replicate in phloem cells of a few species within the family Rutaceae and to transmission by a few aphid species, CTV and citrus probably coevolved for centuries at the site of origin of citrus plants. CTV dispersal to other regions and its interaction with new scion varieties and rootstock combinations resulted in three distinct syndromes named tristeza, stem pitting and seedling yellows. The first, inciting decline of varieties propagated on sour orange, has forced the rebuilding of many citrus industries using tristeza-tolerant rootstocks. The second, inducing stunting, stem pitting and low bearing of some varieties, causes economic losses in an increasing number of countries. The third is usually observed by biological indexing, but rarely in the field. CTV polar virions are composed of two capsid proteins and a single-stranded, positive-sense genomic RNA (gRNA) of approximately 20 kb, containing 12 open reading frames (ORFs) and two untranslated regions (UTRs). ORFs 1a and 1b, encoding proteins of the replicase complex, are directly translated from the gRNA, and together with the 5' and 3'UTRs are the only regions required for RNA replication. The remaining ORFs, expressed via 3'-coterminal subgenomic RNAs, encode proteins required for virion assembly and movement (p6, p65, p61, p27 and p25), asymmetrical accumulation of positive and negative strands during RNA replication (p23), or suppression of post-transcriptional gene silencing (p25, p20 and p23), with the role of proteins p33, p18 and p13 as yet unknown. Analysis of genetic variation in CTV isolates revealed (1) conservation of genomes in distant geographical regions, with a limited repertoire of genotypes, (2) uneven distribution of variation along the gRNA, (3) frequent recombination events and (4) different selection pressures shaping CTV populations. Measures to control CTV damage include quarantine and budwood certification programmes, elimination of infected trees, use of tristeza-tolerant rootstocks, or cross protection with mild isolates, depending on CTV incidence and on the virus strains and host varieties predominant in each region. Incorporating resistance genes into commercial varieties by conventional breeding is presently unfeasible, whereas incorporation of pathogen-derived resistance by plant transformation has yielded variable results, indicating that the CTV-citrus interaction may be more specific and complex than initially thought. A deep understanding of the interactions between viral proteins and host and vector factors will be necessary to develop reliable and sound control measures.
柑橘衰退病毒(CTV)(纤毛病毒属,长线形病毒科)是引发毁灭性疫情的病原体,改变了柑橘产业的发展进程。CTV适应在芸香科少数物种的韧皮部细胞中复制,并通过少数蚜虫物种传播,它与柑橘可能在柑橘植物的起源地共同进化了几个世纪。CTV传播到其他地区,并与新的接穗品种和砧木组合相互作用,导致了三种不同的症状,即衰退、茎陷点和幼苗黄化。第一种症状导致以酸橙为砧木繁殖的品种衰退,迫使许多柑橘产业使用耐衰退的砧木进行重建。第二种症状导致一些品种生长受阻、茎部出现陷点和结果率低,在越来越多的国家造成经济损失。第三种症状通常通过生物学鉴定观察到,但在田间很少见。CTV的极性病毒粒子由两种衣壳蛋白和一条约20 kb的单链正义基因组RNA(gRNA)组成,该gRNA包含12个开放阅读框(ORF)和两个非翻译区(UTR)。编码复制酶复合体蛋白的ORF 1a和1b直接从gRNA翻译而来,连同5'和3'UTR是RNA复制所需的唯一区域。其余的ORF通过3'共末端亚基因组RNA表达,编码病毒粒子组装和移动所需的蛋白(p6、p65、p61、p27和p25)、RNA复制过程中正链和负链的不对称积累(p23)或转录后基因沉默的抑制(p25、p20和p23),而蛋白p33、p18和p13的作用尚不清楚。对CTV分离株遗传变异的分析表明:(1)在遥远的地理区域基因组具有保守性,基因型种类有限;(2)gRNA上变异分布不均匀;(3)频繁发生重组事件;(4)不同的选择压力塑造了CTV群体。控制CTV危害的措施包括检疫和接穗认证计划、清除受感染的树木、使用耐衰退的砧木或用温和分离株进行交叉保护,具体措施取决于CTV的发病率以及每个地区主要的病毒株和寄主品种。通过常规育种将抗性基因导入商业品种目前不可行,而通过植物转化导入病原体衍生的抗性则产生了不同的结果,这表明CTV与柑橘的相互作用可能比最初认为的更加特异和复杂。要制定可靠且合理的控制措施,深入了解病毒蛋白与寄主及介体因子之间的相互作用是必要的。