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Eradication of latent viruses from apple cultivar `Monalisa' shoot tips using droplet-vitrification cryotherapy

机译:使用液滴 - 玻璃化冷冻疗法消除苹果品种`Monalisa'拍摄提示的潜伏病毒

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In apple, virally transmitted diseases cause economic losses as a result of their direct effect on production and yield and by causing an increased susceptibility to other phytopathogenic agents. This study evaluated the effectiveness of a droplet-vitrification cryopreservation technique in eradicating latent viruses: Apple chlorotic leaf spot virus (ACLSV), Apple stem grooving virus (ASGV) and Apple stem pitting virus (ASPV) from in vitro axillary shoot tips excised from 'SC417 Monalisa' apple cultivar shoot tips. In vitro stock cultures, four weeks after subculture, infected with ASGV, ASPV and ACLSV were used as source material. Axillary shoot tips were excised from stock cultures, precultured in MS + 2 M glycerol + 0.8 M sucrose, and then exposed to plant vitrification solution 2 (PVS2) for between 0 and 80 min (six treatments) at 0 degrees C or room temperature prior to liquid nitrogen (LN) exposure. Shoot tips were then warmed and recovered on growth medium. The survival and regrowth of cryopreserved (+ LN) and non-cryopreserved (-LN) 'Monalisa' shoot tips were evaluated and the efficiency of virus eradication was determined using RT-PCR after recovered plants were grown in a greenhouse for 6 months. With this protocol, the highest degree of regrowth (45%) were obtained after 20 to 40 min PVS2 exposure at room temperature. After 6 months of growth in a greenhouse, all of the plants regenerated after cryopreservation were free of ASPV, 95% were free of ACLSV, and 35% were free of ASGV. This promising cryotherapy procedure may facilitate the production of virus-free plants.
机译:在苹果中,病毒传播的疾病导致经济损失导致其直接影响生产和产量,并导致对其他植物致病剂的易感性增加。该研究评估了液滴 - 玻璃化冷冻保存技术在消除潜伏病毒中的有效性:苹果氯化叶片斑点病毒(ACLSV),苹果茎槽病毒(ASGV)和苹果茎点状病毒(ASPV)来自体外腋窝射击提示' SC417 Monalisa'苹果品种射击提示。在体外股票培养物,亚培养后四周,感染ASGV,ASPV和ACLSV被用作源材料。从库存培养物,在MS + 2M甘油+ 0.8M蔗糖中预测,然后在0℃或室温下暴露于植物玻璃化溶液2(PVS2)的植物玻璃化溶液2(PVS2)的腋下射击尖端。液氮(LN)暴露。然后在生长培养基上升温并回收射击尖端。评估冷冻保存(+ LN)和非冷冻保存(-LN)'Monalisa'拍摄提示的存活率和再生,并在温室生长6个月后使用RT-PCR测定病毒根除的效率。通过该方案,在室温下在20至40分钟的PVS2暴露后获得最高程度的再生(45%)。在温室的温室增长6个月后,冷冻保存后再再生的所有植物都没有ASPV,95%没有ACLSV,35%没有ASGV。这种有前途的冷冻疗法可以促进无病毒植物的生产。

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