首页> 外文期刊>Acta Horticulturae >Improved molecular methods for detection of European stone fruit yellows (ESFY) phytoplasmas from in vitro shoots of fruit trees.
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Improved molecular methods for detection of European stone fruit yellows (ESFY) phytoplasmas from in vitro shoots of fruit trees.

机译:从果树体外芽中检测欧洲核果黄(ESFY)植物质原的改进分子方法。

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摘要

Prunus species are prone to infections by viruses and phytoplasmas, against which no effective cure exists for already infected plants in the field. Phytoplasmas infecting fruit trees can cause severe symptoms and are considered as quarantine organisms in Europe and North America. However, detection often is hampered by their irregular distribution in host plants. In the frame of phytosanitary measures a sensitive, specific and quick detection system would be highly desirable for routine detection, mainly to avoid the use of infected planting material. The development of improved strategies for the production of elite plants of phytoplasma-free stone fruit cultivars to be used for the production of certified elite propagation material was achieved. In vitro thermotherapy and meristem culture to eliminate pathogens from stone fruit plants were applied and protocols were validated for survival rates of shoots and plants and on their effectiveness for pathogen elimination. To gain time and to confirm the elimination of these pathogens from planting material by the applied in vitro treatments, improved detection methods were tested on micropropagated material soon after the treatment. The use of diverse general primers in bi-nested PCR allows to detect phytoplasmas belonging to different groups. Broad spectrum PCR are advisable for fruit tree material in micropropagation when the sanitary status of the mother plants is not known, while specific PCR primers could be employed to detect the presence of a known phytoplasma.
机译:李属物种容易被病毒和植物原虫感染,在田间已经没有针对其的有效治愈方法。感染果树的植原体会引起严重的症状,在欧洲和北美被认为是检疫生物。但是,检测常常因其在寄主植物中的不规则分布而受阻。在植物检疫措施的框架内,非常需要灵敏,特异和快速的检测系统来进行常规检测,主要是避免使用被感染的种植材料。实现了改进的策略,以生产用于生产经认证的优良繁殖材料的无植物抗核果核品种的优良植物。应用体外热疗法和分生组织培养从核果类植物中清除病原体,并验证了方案对芽和植物的存活率及其对病原体清除的有效性。为了增加时间并确认通过应用体外处理从种植材料中消除了这些病原体,在处理后不久对微繁材料进行了改进的检测方法测试。在双巢式PCR中使用多种通用引物可以检测属于不同组的植物质原体。当母本植物的卫生状况未知时,建议对微繁殖中的果树材料使用广谱PCR,而特定的PCR引物可用于检测已知植物质体的存在。

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