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首页> 外文期刊>Research on Crops >Feasibility of meristem culture for management of Banana Streak Virus (BSV) through micropropagation.
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Feasibility of meristem culture for management of Banana Streak Virus (BSV) through micropropagation.

机译:分生组织培养通过微繁殖处理香蕉条纹病毒(BSV)的可行性。

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摘要

Meristem culture is considered as novel approach of biotechnology in eliminating plant viruses in vitro. However, the spread of Banana streak virus (BSV) through tissue culture seedlings in the field had doubt about the technique. The present study was conducted to check the feasibility of the technology in managing the BSV through meristem culture and in combination with thermotherapy. BSV-infected suckers of two banana cultivars (Grand nine and Ardhapuri) were used for meristem culture along with the respective controls. Hot water treatment was supplemented as a tool to suppress the virus. Meristem buds were treated at different temperatures and time intervals. Buds sustained the maximum temperature of 50 degrees C for 10 min only and were selected for further regeneration after excising meristem from them. Non-treated infested meristems were also inoculated along with healthy meritames on MS medium supplemented with different growth regulators for different stages. The regeneration of BSV-infested meristem was found abnormal and took more time than that of healthy meristems. The hot water-treated suckers took the longest time. The regenerated seedlings subjected to PCR confirmation showed the inability of meristem culture technique in eliminating the virus from the host. The episomal nature of the virus and its genomic integration into the host genome could be the possible reason for the failure of the technology. Proper indexing by ELISA or PCR and regular observation of the explant for certain period of time were found most ideal before selecting the explants for tissue culture. Strict quarantine while international exchange of germplasm was the most ideal procedure to avoid subcontinental movement of the virus through exchange materials.
机译:分生组织培养被认为是生物技术在体外消除植物病毒的一种新方法。然而,在田间通过组织培养苗香蕉条状病毒(BSV)的传播对该技术产生了怀疑。进行本研究以检查该技术通过分生组织培养并结合热疗法管理BSV的可行性。使用感染了BSV的两个香蕉品种(大9号和Ardhapuri)的吸盘以及相应的对照进行分生组织培养。补充了热水处理作为抑制病毒的工具。分生组织芽在不同的温度和时间间隔下处理。芽仅在50°C的最高温度下维持10分钟,并从其中切下分生组织后选择进行进一步再生。未治疗的受感染的分生组织也与健康的功分一起接种在MS培养基上,该培养基在不同阶段补充了不同的生长调节剂。发现受BSV感染的分生组织的再生异常,并且比健康的分生组织需要更多的时间。热水吸盘花费的时间最长。经过PCR确证的再生幼苗显示分生组织培养技术无法消除宿主病毒。病毒的附加性质及其将基因组整合到宿主基因组中可能是该技术失败的可能原因。在选择外植体进行组织培养之前,最理想的方法是通过ELISA或PCR正确标引并在一定时期内定期观察外植体。进行国际种质交换时要进行严格的检疫,这是避免病毒通过交换材料进行亚大陆运动的最理想方法。

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