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基于 RNA 干扰的外源双链 RNA 赋予烟草对 Rhizoctonia solani AG-3 的抗性。

RNA interference-based exogenous double-stranded RNAs confer resistance to Rhizoctonia solani AG-3 on Nicotiana tabacum.

机构信息

Liaoning Key Laboratory of Plant Pathology, College of Plant Protection, Shenyang Agricultural University, Shenyang, China.

Sichuan Province Tobacco Company, Chengdu, China.

出版信息

Pest Manag Sci. 2024 Apr;80(4):2170-2178. doi: 10.1002/ps.7962. Epub 2024 Jan 29.

DOI:10.1002/ps.7962
PMID:38284497
Abstract

BACKGROUND

Rhizoctonia solani Kühn is a pathogenic fungus causing tobacco target spot disease, and leads to great losses worldwide. At present, resistant varieties and effective control strategy on tobacco target spot disease are very limited. Host-induced gene silencing (HIGS) as well as the exogenous dsRNA can be used to suppress disease progression, and reveal the function of crucial genes involved in the growth and pathogenesis of the fungus.

RESULTS

The silencing of endoPGs or RPMK1 in host plants by TRV-based HIGS resulted in a significant reduction in disease development in Nicotiana benthamiana. In vitro analysis validated that red fluorescence signals were consistently observed in the hyphae treated with Cy3-fluorescein-labeled dsRNA at 12, 24, 48 and 72 h postinoculation (hpi). Additionally, application of dsRNA-endoPGs, dsRNA-RPMK1 and dsRNA-PGMK (fusion of partial endoPGs and RPMK1 sequences) effectively inhibited the hyphal growth of R. solani YC-9 in vitro and suppressed disease progression in the leaves, and quantitative real-time PCR confirmed that the application of dsRNAs significantly reduced the expression levels of endoPGs and RPMK1.

CONCLUSION

These results provide theoretical basis and new direction for RNAi approaches on the prevention and control of disease caused by R. solani. © 2024 Society of Chemical Industry.

摘要

背景

立枯丝核菌(Rhizoctonia solani Kühn)是一种致病真菌,可导致烟草靶斑病,给全世界造成巨大损失。目前,对于烟草靶斑病,抗性品种和有效的控制策略非常有限。宿主诱导基因沉默(HIGS)以及外源 dsRNA 可用于抑制病情进展,并揭示与真菌生长和发病机制相关的关键基因的功能。

结果

TRV 介导的 HIGS 沉默宿主植物中的内 PGs 或 RPMK1 可显著降低烟草原生质体中靶斑病的发展。体外分析验证,在接种后 12、24、48 和 72 h 用 Cy3-荧光素标记的 dsRNA 处理菌丝时,始终观察到红色荧光信号。此外,dsRNA-endoPGs、dsRNA-RPMK1 和 dsRNA-PGMK(endoPGs 和 RPMK1 序列的部分融合)的应用可有效抑制立枯丝核菌 YC-9 的菌丝体外生长并抑制叶片中的病情进展,定量实时 PCR 证实 dsRNA 的应用可显著降低内 PGs 和 RPMK1 的表达水平。

结论

这些结果为利用 RNAi 方法防治立枯丝核菌引起的疾病提供了理论依据和新方向。© 2024 化学工业协会。