浙江农业科学 ›› 2026, Vol. 67 ›› Issue (8): 2080-2085.DOI: 10.16178/j.issn.0528-9017.20260444

• 综述 • 上一篇    下一篇

甘薯脱毒与组培苗长期保存技术的研究进展

吴宜凡()   

  1. 杭州市农业科学研究院,浙江 杭州 310024
  • 收稿日期:2026-06-15 出版日期:2026-08-11 发布日期:2026-08-20
  • 作者简介:吴宜凡,研究方向为旱粮育种与栽培。E-mail:wuyifan9877@163.com
  • 基金资助:
    2024年度农业与社会发展领域公益性科研引导项目(20241029Y002)

Research progress on virus elimination and long-term preservation of tissue-cultured sweet potato plantlets

WU Yifan()   

  1. Hangzhou Academy of Agricultural Sciences,Hangzhou 310024,Zhejiang
  • Received:2026-06-15 Online:2026-08-11 Published:2026-08-20

摘要:

甘薯作为我国重要的粮食作物与工业原料,其无性繁殖特性导致病毒病在植株体内代际累积,严重制约了产业的可持续发展。脱毒组培苗技术是防控病毒病的核心手段,但脱毒效率的品种依赖性、病毒再感染风险以及组培苗长期保存技术的滞后,已成为限制优良种源持续供应的关键瓶颈。本文系统综述了甘薯脱毒与组培苗长期保存技术的研究进展,重点整合了病毒复合侵染特征与传播机制、茎尖分生组织培养技术的多元化优化路径、脱毒苗等级评价与繁育体系建设、病毒检测技术的集成应用以及超低温保存技术的探索实践。研究表明:甘薯病毒病的复合侵染具有普遍性,媒介昆虫的协同防控与脱毒种苗生产密不可分;外源激素调控、品种特异性方案开发以及光质等物理因子的引入,推动脱毒技术从单一茎尖培养向多因素协同优化演进;脱毒苗分级标准的确立和微型薯育苗等技术创新,有效提升了移栽成活率与周年供应能力;病毒检测已形成初筛与确证相结合的组合策略,并逐步纳入品种推广的标准规程。在长期保存方面,传统继代培养的局限性日益突出,以玻璃化法为代表的超低温保存技术展现出应用前景,但冻后存活率提升和遗传稳定性监测仍是亟待突破的核心难题。当前研究正从单一技术突破向系统集成创新转变,未来应聚焦广谱抗病毒策略的源头创新、超低温保存体系的标准化建立以及保存后材料遗传稳定性的长期监测,推动脱毒技术先进性与保存技术可靠性的深度融合,为甘薯种业高质量发展和种质资源安全保存提供理论支撑。

关键词: 甘薯, 脱毒, 组织培养, 病毒检测, 种质资源

Abstract:

As a major food crop and industrial raw material in China,sweet potato faces serious constraints to sustainable industrial development due to the intergenerational accumulation of viral diseases caused by its asexual propagation. Virus-free tissue culture technology is the core means for controlling viral diseases;however,the variety dependence of virus elimination efficiency,the risk of virus re-infection,and the lag in long-term preservation technology for tissue-cultured plantlets have become key bottlenecks limiting the continuous supply of elite germplasm. This paper systematically reviews the research progress on virus elimination and long-term preservation of tissue-cultured sweet potato plantlets,with a focus on integrating the characteristics and transmission mechanisms of mixed virus infections,diversified optimization pathways for shoot tip meristem culture,establishment of grading evaluation and propagation systems for virus-free plantlets,integrated application of virus detection technologies,and exploratory practices in cryopreservation. The review indicates that mixed infection of sweet potato viral diseases is common,and the coordinated control of vector insects is inseparable from the production of virus-free seedlings. The introduction of exogenous hormone regulation,development of variety-specific protocols,and incorporation of physical factors such as light quality have driven the evolution of virus elimination technology from single shoot tip culture to multi-factor synergistic optimization. The establishment of grading standards for virus-free plantlets and innovations such as mini-tuber seedling production have effectively improved transplant survival rates and year-round supply capacity. Virus detection has formed a combined strategy of preliminary screening and confirmatory testing,and is gradually being incorporated into standard procedures for variety promotion. Regarding long-term preservation,the limitations of traditional subculture are becoming increasingly prominent,and cryopreservation technologies,represented by the vitrification method,show application prospects;however,improving post-thaw survival rates and monitoring genetic stability remain core challenges that urgently need to be addressed. Current research is shifting from single-technology breakthroughs to systematic integrated innovation. Future efforts should focus on the original innovation of broad-spectrum antiviral strategies,the standardization of cryopreservation systems,and long-term monitoring of genetic stability of post-preservation materials,so as to promote the deep integration of advanced virus elimination technology and reliable preservation technology,thereby providing theoretical support for the high-quality development of the sweet potato seed industry and the safe conservation of germplasm resources.

Key words: sweet potato, virus elimination, tissue culture, virus detection, germplasm resources

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