German-Retana Sylvie, Walter Jocelyne, Le Gall Olivier
UMR1090 Génomique Diversité Pouvoir Pathogène, INRA Université de Bordeaux 2, F-33883 Villenave D'Ornon, France.
Mol Plant Pathol. 2008 Mar;9(2):127-36. doi: 10.1111/j.1364-3703.2007.00451.x.
Lettuce mosaic virus (LMV) belongs to the genus Potyvirus (type species Potato virus Y) in the family Potyviridae.
The virion is filamentous, flexuous with a length of 750 nm and a width of 15 nm. The particles are made of a genomic RNA of 10 080 nucleotides, covalently linked to a viral-encoded protein (the VPg) at the 5' end and with a 3' poly A tail, and encapsidated in a single type of capsid protein. The molecular weight of the capsid protein subunit has been estimated electrophoretically to be 34 kDa and estimated from the amino acid sequence to be 31 kDa.
The genome is expressed as a polyprotein of 3255 amino-acid residues, processed by three virus-specific proteinases into ten mature proteins.
LMV has a worldwide distribution and a relatively broad host range among several families. Weeds and ornamentals can act as local reservoirs for lettuce crops. In particular, many species within the family Asteraceae are susceptible to LMV, including cultivated and ornamental species such as common (Lactuca sativa), prickly (L. serriola) or wild (L. virosa) lettuce, endive/escarole (Cichorium endiva), safflower (Carthamus tinctorius), starthistle (Centaurea solstitialis), Cape daisy (Osteospermum spp.) and gazania (Gazania rigens). In addition, several species within the families Brassicaceae, Cucurbitaceae, Fabaceae, Solanaceae and Chenopodiaceae are natural or experimental hosts of LMV. Genetic control of resistance to LMV: The only resistance genes currently used to protect lettuce crops worldwide are the recessive genes mo1(1) and mo1(2) corresponding to mutant alleles of the gene encoding the translation initiation factor eIF4E in lettuce. It is believed that at least one intact copy of eIF4E must be present to ensure virus accumulation.
LMV is transmitted in a non-persistent manner by a high number of aphid species. Myzus persicae and Macrosiphum euphorbiae are particularly active in disseminating this virus in the fields. LMV is also seedborne in lettuce. The effectiveness of LMV transmission depends on the cultivar and the age of the seed carrier at the inoculation time.
The characteristic symptoms on susceptible lettuce cultivars are dwarfism, mosaic, distortion and yellowing of the leaves with sometimes a much reduced heart of lettuce (failure to form heads). The differences in virus strains, cultivars and the physiological stage of the host at the moment of the attack cause different symptom severity: from a very slight discoloration of the veins to severe necrosis leading to the death of the plant.
莴苣花叶病毒(LMV)属于马铃薯Y病毒科中的马铃薯Y病毒属(模式种为马铃薯Y病毒)。
病毒粒子呈丝状,弯曲状,长度为750纳米,宽度为15纳米。粒子由一条10080个核苷酸的基因组RNA组成,在5'端与病毒编码的蛋白质(VPg)共价连接,并带有3' poly A尾,且被包裹在单一类型的衣壳蛋白中。衣壳蛋白亚基的分子量经电泳估计为34 kDa,从氨基酸序列估计为31 kDa。
基因组表达为一个由3255个氨基酸残基组成的多聚蛋白,经三种病毒特异性蛋白酶加工成十种成熟蛋白。
LMV在全球范围内分布,在多个科中具有相对广泛的寄主范围。杂草和观赏植物可作为生菜作物的本地病毒库。特别是,菊科中的许多物种对LMV敏感,包括栽培和观赏物种,如普通生菜(生菜)、刺叶生菜(刺叶莴苣)或野生生菜(毒莴苣)、苦苣/宽叶苦苣(菊苣)、红花(红花)、矢车菊(夏至草)、南非万寿菊(蓝目菊属)和勋章菊(勋章菊)。此外,十字花科、葫芦科、豆科、茄科和藜科中的几个物种是LMV的天然或实验寄主。对LMV抗性的遗传控制:目前全球用于保护生菜作物的唯一抗性基因是隐性基因mo1(1)和mo1(2),它们对应于生菜中编码翻译起始因子eIF4E的基因突变等位基因。据信,必须存在至少一个完整的eIF4E拷贝以确保病毒积累。
LMV由大量蚜虫以非持久性方式传播。桃蚜和茄无网蚜在田间传播这种病毒方面特别活跃。LMV也可通过种子传播到生菜中。LMV传播的有效性取决于品种和接种时种子携带病毒的种子载体的年龄。
易感生菜品种的典型症状是矮化、花叶、叶片扭曲和黄化,有时生菜的心叶会大大减少(无法形成叶球)。病毒株系、品种以及寄主在受侵染时的生理阶段的差异会导致症状严重程度不同:从叶脉非常轻微的变色到严重坏死导致植物死亡。