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A novel approach for developing resistance in rice against phloem limited viruses by antagonizing the phloem feeding hemipteran vectors

机译:通过拮抗韧皮部饲喂的半足动物载体来发展水稻对韧皮部有限病毒的抗性的新方法

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摘要

Rice production is known to be severely affected by virus transmitting rice pests, brown planthopper (BPH) and green leafhopper (GLH) of the order hemiptera, feeding by phloem abstraction. ASAL, a novel lectin from leaves of garlic (Allium sativum) was previously demonstrated to be toxic towards hemipteran pests when administered in artificial diet as well as in ASAL expressing transgenic plants. In this report ASAL was targeted under the control of phloem-specific Agrobacterium rolC and rice sucrose synthase-1 (RSs1) promoters at the insect feeding site into popular rice cultivar, susceptible to hemipteran pests. PCR, Southern blot and C-PRINS analyses of transgenic plants have confirmed stable T-DNA integration and the transgenes were co-segregated among self-fertilized progenies. The T(0) and T(1) plants, harbouring single copy of intact T-DNA expression cassette, exhibit stable expression of ASAL in northern and western blot analyses. ELISA showed that the level of expressed ASAL was as high as 1.01% of total soluble protein. Immunohistofluorescence localization of ASAL depicted the expected expression patterns regulated by each promoter type. In-planta bioassay studies revealed that transgenic ASAL adversely affect survival, growth and population of BPH and GLH. GLH resistant T(1) plants were further evaluated for the incidence of tungro disease, caused by co-infection of GLH vectored Rice tungro bacilliform virus (RTBV) and Rice tungro spherical virus (RTSV), which appeared to be dramatically reduced. The result presented here is the first report of such GLH mediated resistance to infection by RTBV/RTSV in ASAL expressing transgenic rice plant.
机译:已知水稻的生产受到病毒传播的水稻害虫,半翅目的褐飞虱(BPH)和绿叶蝉(GLH)的严重影响,并通过韧皮部提取为食。 ASAL是一种从大蒜(大蒜)叶片中提取的新型凝集素,以前在人工饮食和表达ASAL的转基因植物中施用时,对半足类害虫具有毒性。在本报告中,ASAL在韧皮部特有的农杆菌rolC和水稻蔗糖合酶-1(RSs1)启动子的控制下,在昆虫的取食部位进入流行的水稻品种,易受半球虫害。对转基因植物的PCR,Southern印迹和C-PRINS分析已证实稳定的T-DNA整合,并且转基因在自体受精子代中共分离。 T(0)和T(1)植物具有完整的T-DNA表达盒的单个拷贝,在北部和西部印迹分析中显示出ASAL的稳定表达。 ELISA显示,表达的ASAL水平高达总可溶性蛋白的1.01%。 ASAL的免疫组织荧光定位描述了每种启动子类型调控的预期表达模式。植物体内生物测定研究表明,转基因ASAL对BPH和GLH的存活,生长和种群产生不利影响。进一步评估了GLH抗性T(1)植物的真菌感染率,这些疾病是由GLH载体水稻真菌水稻杆状杆菌病毒(RTBV)和水稻真菌球状病毒(RTSV)共同感染引起的,其发病率明显降低。此处呈现的结果是这种GLH介导的在表达ASAL的转基因水稻植物中RTBV / RTSV感染抵抗力的首次报道。

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