The use of transgenic fruit trees as a resistance strategy for virus epidemics: the plum pox (sharka) model

被引:35
|
作者
Ravelonandro, M
Scorza, R
Callahan, A
Levy, L
Jacquet, C
Monsion, M
Damsteegt, V
机构
[1] INRA, Ctr Rech Bordeaux, Pathol Vegetale Stn, F-33883 Villenave Dornon, France
[2] ARS, Appalachian Fruit Res Stn, USDA, Kearneysville, WV USA
[3] APHIS Plant Protect & Quarantine Plant Methods La, Beltsville, MD USA
[4] ARS, USDA, Ft Detrick, MD USA
关键词
Prunus domestica; Plum pox virus; pathogen-derived-resistance; co-suppression;
D O I
10.1016/S0168-1702(00)00188-X
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Sharka or plum pox, caused by Plum pox virus (PPV: genus Potyvirus; Family Potyviridae), is the most serious disease of Prunus. Most cultivated Prunus species are highly susceptible and conventional breeding has not produced highly resistant and commercially acceptable varieties. Success in developing virus-resistant herbaceous crops through genetic engineering led us to investigate this approach for resistance to PPV. Our programme aims to develop a biotechnological approach to PPV control that is effective and shown to be environmentally safe. The programme began with the cloning of the PPV coat protein (CP) gene and the development of a transformation system for plum (Prunus domestica). The CP construct was first tested in Nicotiana benthamiana in which it proved effective in producing transgenic plants with varying levels of CP expression. Some of these plants, particularly low PPV CP expressers, were resistant to PPV, or recovered from initial infection. Based on these results plum was transformed using the Agrobacterium tumefaciens system and both low and high PPV CP-expressing transgenic plum lines were obtained. These were inoculated with PPV by bud grafts in the greenhouse. Line C-5 proved to be highly resistant. It contained multiple copies of the insert, produced low levels of PPV CP mRNA, no detectable CP and the insert appeared to be methylated. These characteristics all suggest that the resistance of the C-5 clone is based on post-transcriptional gene silencing (PTGS). Field tests of C-5 and other transgenic lines in Poland, Romania and Spain have demonstrated that such trees when inoculated by bud-grafts allow a low level of PPV multiplication, from which they rapidly recover. C-5 plants exposed to natural infection for 3 years did not become infected, whereas control trees were infected in the first year. Hybrid plums having the C-5 PPV CP insert inherited from C-5 are virus-resistant, demonstrating the usefulness of C-5 as a parent in developing new PPV-resistant plum varieties. Research is in progress on the biorisks of PPV CP transgenic plants. Gene constructs that either produce no CP or CP that cannot be transmitted by aphids have been developed, tested in N. benthamiana and transferred to plum. Studies have begun on the potential for synergistic interactions between the PPV CP gene and the other common viruses of Prunus spp. In the future we will be participating in investigating the toxicity or/and the allergenicity of transgenic fruit products and, more importantly, transgenic lines will be developed that express transgenes only in vegetative parts of the plant and not in the fruit. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:63 / 69
页数:7
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