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首页> 外文期刊>Acta Horticulturae >Euphorbia pulcherrima. Methods to eliminate poinsettia mosaic virus (PNMV) and reinfection by different methods to reveal the 'nature' of the branching factor
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Euphorbia pulcherrima. Methods to eliminate poinsettia mosaic virus (PNMV) and reinfection by different methods to reveal the 'nature' of the branching factor

机译:一品红。消除一品红花叶病毒(PNMV)并通过不同方法再​​感染以揭示分支因子“性质”的方法

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摘要

A survey on the incidence of poinsettia mosaic tymovirus (PnMV) in E. pulcherrima cultivars from Danish growers, as well as imported cultivars, revealed that PnMV was present in all plants tested. PnMV was eliminated by 2 methods, meristem-tip culture of the cultivar Freedom or temp. treatment of Lilo mother plants. The 2 methods for elimination of PnMV in Freedom and Lilo, respectively, resulted in very different plants. Meristem-tip culture gave restricted-branching (r-b) plants with thicker stems and dark, lobed leaves and more intense red bracts when compared with the original Freedom plant. Offspring from the temp. treated Lilo could not be distinguished from the original clone. The plants were repeatedly tested for PnMV. Reinfection of meristem-cultured plants by grafting to the original infected branching plant and by sap-inoculation with PnMV from different sources was carried out. In cuttings from plants which became reinfected branching was recorded. Branching and PnMV were re-established in meristem plants after approach grafting of the 2 possible combinations of virus-free r-b plants to the original PnMV infected branching plant. The branching agent moved up- and downwards from the grafting site. Sap-inoculation with PnMV did not reintroduce branching. These results indicate that the branching was caused by a biological agent, different from PnMV, which has not yet been identified.
机译:对来自丹麦种植者和进口种植者的大叶大肠杆菌(E. pulcherrima)品种中的一品红花叶病毒(PnMV)发生率的调查显示,所有测试的植物中均存在PnMV。通过两种方法消除了PnMV,即品种自由或温度的分生组织尖端培养。处理荔枝母本。分别在Freedom和Lilo中消除PnMV的两种方法导致了非常不同的植物。与原始的Freedom植物相比,分生组织尖端培养产生的限制分支(r-b)植物具有较粗的茎和深色,浅裂的叶子,且红色intense片更强。从温度的后代。经过处理的Lilo无法与原始克隆区分开。重复测试植物的PnMV。通过嫁接到原始感染的分支植物上并用不同来源的PnMV液汁接种来对分生组织培养的植物进行再感染。在被重新感染的植物的插条中记录了分支。在将两种可能的无病毒r-b植物组合移植到原始感染PnMV的分支植物后,在分生组织植物中重新建立了分支和PnMV。支化剂从接枝部位上下移动。用PnMV汁液接种不会重新引入分支。这些结果表明,该分支是由尚未鉴定的不同于PnMV的生物因子引起的。

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