Department of Agricultural Biotechnology, Tarbiat Modares University, Tehran, Iran.
Agricultural Biotechnology Research Institute of Iran (ABRII), Karaj, Iran.
Sci Rep. 2022 Sep 2;12(1):14948. doi: 10.1038/s41598-022-19269-3.
One of the world's main horticulture problems is the contamination of fruit trees with a variety of plant diseases, especially viral and pseudo-viral diseases. Due to the non-sexual propagation of the trees, these diseases have been transmitted to different parts of the world. The main aim of this study was to obtain a new effective method for virus elimination from almond cultivars, which was performed in two phases. In the first phase, we tested various almond cultivars with ELISA and RT-PCR. The results showed the infection of mother plantlets. So, three types of in vitro thermotherapy treatments were performed on infected plants to make them virus-free. The plantlets obtained from 0.5 mm meristem treated with the first type of thermotherapy (TH1: 8 h at 27 °C and 16 h at 38 °C for 18 days) showed the highest percentage of elimination of ApM, ACLS and TRS viruses. In the second phase, meristems were cultured on MS medium containing 0, 0.5, 1 and 2 mg/L 2,4-D with 1 mg/L TDZ and after two weeks, thermotherapy treatments were performed. The results showed, combining three methods of thermotherapy (TH1), meristem culture and somatic embryogenesis induction from meristem on MS medium supplemented with 0.5 mg/L 2,4-D and 1 mg/L TDZ is the most effective and safe technique for virus eradication without meristem size challenges. The samples that were diagnosed as virus-free were proliferated in temporary immersion bioreactor systems, and rooted to be used for later propagation and establishment of mother healthy orchards.
世界园艺面临的主要问题之一是各种植物病害,尤其是病毒性和类病毒病害对果木的污染。由于树木的非有性繁殖,这些病害已经传播到世界不同地区。本研究的主要目的是获得一种从巴旦木品种中有效去除病毒的新方法,该方法分两个阶段进行。在第一阶段,我们用 ELISA 和 RT-PCR 对各种巴旦木品种进行了测试。结果表明母本植株受到感染。因此,对感染的植株进行了三种体外热疗处理,使其无病毒。用第一类热疗(TH1:27°C 处理 8 小时,38°C 处理 16 小时,共 18 天)处理 0.5mm 茎尖的植株获得的植株,ApM、ACLS 和 TRS 病毒的去除率最高。在第二阶段,将茎尖在含有 0、0.5、1 和 2mg/L 2,4-D 和 1mg/L TDZ 的 MS 培养基上培养,两周后进行热疗处理。结果表明,将三种热疗(TH1)方法、茎尖培养和在补充有 0.5mg/L 2,4-D 和 1mg/L TDZ 的 MS 培养基上由茎尖诱导体细胞胚发生相结合,是最有效和安全的技术,可在不影响茎尖大小的情况下彻底消除病毒。诊断为无病毒的样本在暂态浸没生物反应器系统中增殖,并生根,用于后续繁殖和建立健康母果园。