Sidorova Tatiana, Mikhailov Roman, Pushin Alexander, Miroshnichenko Dmitry, Dolgov Sergey
Branch of Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Puschino, Russia.
Nikita Botanical Gardens - National Scientific Centre, Russian Academy of Sciences, Yalta, Russia.
Front Plant Sci. 2019 Mar 12;10:286. doi: 10.3389/fpls.2019.00286. eCollection 2019.
In modern horticulture (PPV) imposes serious threats to commercial plantations of a wide range of fruit species belonging to genera . Given the lack of natural genetic resources, which display reliable resistance to PPV infection, there has been considerable interest in using genetic engineering methods for targeted genome modification of stone fruit trees to control Sharka disease caused by PPV. Among the many virus defense mechanisms, RNA interference is shown to be the most promising transgenic disease-control strategy in plant biotechnology. The present study describes the production of transgenic PPV resistant European plum "Startovaya" ( L.) through the -mediated transformation of leaf explants. Due to organogenesis from leaves, the established protocol allows the genetic engineering of the plum genome without losing clonal fidelity of original cultivar. Seven independent transgenic plum lines containing the self-complementary fragments of PPV-CP gene sequence separated by a PDK intron were generated using as a selective gene and as a reporter gene. The transformation was verified through the histochemical staining for β-glucuronidase activity, PCR amplification of appropriate vector products from isolated genomic DNA and Southern blot analysis of hairpin PPV-CP gene fragments. To clarify the virus resistance, plum buds infected by PPV-M strain were grafted onto 1-year-old transgenic plants, which further were grown into mature trees in the greenhouse. As evaluated by RT-PCR, DAS-ELISA, Western blot, ImmunoStrip test, and visual observations, GM plum trees remained uninfected over 9 years. Infected branches that developed from grafted buds displayed obvious symptoms of Sharka disease over the years and maintained the high level of virus accumulation, whereby host transgenic trees had been constantly challenged with the pathogen. Since the virus was unable to spread to transgenic tissues, the stable expression of PPV-derived gene construct encoding intron-spliced hairpin RNAs provided a highly effective protection of plum trees against permanent viral infection. At the same time, this observation indicates the lack of the systemic spread of resistance from GM tissues to an infected plum graft even after years of joint growth.
在现代园艺中,李痘病毒(PPV)对多种属于李属的水果品种的商业种植园构成严重威胁。由于缺乏对PPV感染具有可靠抗性的天然遗传资源,人们对利用基因工程方法对核果类果树进行靶向基因组修饰以控制由PPV引起的李痘病产生了浓厚兴趣。在众多病毒防御机制中,RNA干扰被证明是植物生物技术中最有前景的转基因疾病控制策略。本研究描述了通过农杆菌介导的欧洲李“Startovaya”(Prunus domestica L.)叶片外植体转化来生产抗PPV转基因植株。由于叶片的器官发生,所建立的方案允许对李基因组进行基因工程改造,而不会丧失原始品种的克隆保真度。使用潮霉素作为选择基因和GUS作为报告基因,产生了七个独立的转基因李株系,这些株系包含由PDK内含子隔开的PPV - CP基因序列的自我互补片段。通过β - 葡萄糖醛酸酶活性的组织化学染色、从分离的基因组DNA中对适当载体产物的PCR扩增以及发夹PPV - CP基因片段的Southern印迹分析来验证转化。为了阐明病毒抗性,将感染PPV - M株系的李芽嫁接到1年生转基因植株上,这些植株随后在温室中长成成年树。通过RT - PCR、DAS - ELISA、Western印迹、免疫试纸条测试和视觉观察评估,转基因李树在9年多的时间里一直未被感染。多年来,从嫁接芽长出的受感染枝条表现出明显的李痘病症状,并保持高水平的病毒积累,从而使宿主转基因树一直受到病原体的挑战。由于病毒无法传播到转基因组织,编码内含子剪接发夹RNA的PPV衍生基因构建体的稳定表达为李树提供了针对永久性病毒感染的高效保护。同时,这一观察结果表明,即使经过多年的共同生长,转基因组织的抗性也不会向受感染的李嫁接体发生系统传播。