Rice-Magnaporthe oryzae arms race: From effector diversification and NLR-mediated immunity to CRISPR-driven durable resistance

IF 5.1 Q1 PLANT SCIENCES
Current Plant Biology Pub Date : 2026-09-01 Epub Date: 2026-08-26 DOI:10.1016/j.cpb.2026.100659
Muhammad Usama Younas, Muhammad Qasim, Irshad Ahmad, Shakal Khan Korai, Gulnaz bibi, Mukhammadjon Ergashev, Mohammed S. Alotaibi, Usman Zulfiqar, Mayank Anand Gururani
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Abstract

Rice blast is a significant threat to global food security and is caused by the virulent fungal pathogen Magnaporthe oryzae, resulting in a loss of about 30 % of the annual yield. This review will present a synthesis of the molecular processes involved in the interaction between rice and M. oryzae, highlighting the evolutionary arms race between the host and the pathogen. The pathogen exploits the genomic plasticity and diversification of the effectors, to avoid being recognized by the host. In contrast, the host immune system operates through two interconnected defense layers: Pattern-triggered immunity (PTI), which serves as the first line of defense, and the effector-triggered immunity (ETI). ETI is mediated by specialized NLR (nucleotide-binding site–leucine-rich repeat) proteins that initiate rapid hypersensitive responses to restrict pathogen invasion. Although more than 146 resistance (R) genes have been described, the review mentions that single-gene resistance is often unsuccessful because of the rapid evolution of pathogens. The transition to gene pyramiding and altering susceptibility (S genes, such as pi21 and bsr-d1, is necessary. Elaborate breeding techniques have also come to depend on the CRISPR/Cas9 system to perform precise multi-locus stacking and disruption of negative regulators, so as to obtain a more durable and broad-spectrum resistance without loss of any yield. Moreover, predictive receptor-effector structure prediction with the aid of artificial intelligence applications like AlphaFold3, combined with pangenomics to harness the lost genetic diversity, is making rice enhancement a predictive, data-oriented science. The review eventually recommends an integrative model that combines multiomics, digital phenotyping, and computational intelligence, to protect the world's rice production under the pressure of the changed environment and pathogens.
水稻-稻瘟病菌军备竞赛:从效应多样化和nlr介导的免疫到crispr驱动的持久抗性
稻瘟病是对全球粮食安全的重大威胁,是由毒力极强的真菌病原体稻瘟病引起的,造成约30%的年产量损失。本文综述了水稻与m.o ryzae相互作用的分子过程,重点介绍了寄主与病原体之间的进化军备竞赛。病原菌利用基因组的可塑性和效应物的多样性,避免被宿主识别。相比之下,宿主免疫系统通过两个相互关联的防御层运作:作为第一道防线的模式触发免疫(PTI)和效应触发免疫(ETI)。ETI是由特殊的NLR(核苷酸结合位点-富含亮氨酸的重复)蛋白介导的,该蛋白启动快速的超敏反应以限制病原体的入侵。尽管已经描述了超过146个耐药基因,但该综述提到,由于病原体的快速进化,单基因耐药往往不成功。过渡到基因金字塔和改变易感性基因(S基因,如pi21和bsr-d1)是必要的。精细的育种技术也依赖于CRISPR/Cas9系统来执行精确的多位点堆叠和负调控因子的破坏,从而在不损失任何产量的情况下获得更持久和广谱的抗性。此外,借助人工智能应用程序(如AlphaFold3)对受体-效应物结构进行预测性预测,并结合泛基因组学来利用失去的遗传多样性,正在使水稻育种成为一门预测性的、以数据为导向的科学。该综述最终推荐了一种结合多组学、数字表型和计算智能的综合模型,以在环境和病原体变化的压力下保护世界水稻生产。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Current Plant Biology
Current Plant Biology Agricultural and Biological Sciences-Plant Science
CiteScore
10.90
自引率
1.90%
发文量
32
审稿时长
50 days
期刊介绍: Current Plant Biology aims to acknowledge and encourage interdisciplinary research in fundamental plant sciences with scope to address crop improvement, biodiversity, nutrition and human health. It publishes review articles, original research papers, method papers and short articles in plant research fields, such as systems biology, cell biology, genetics, epigenetics, mathematical modeling, signal transduction, plant-microbe interactions, synthetic biology, developmental biology, biochemistry, molecular biology, physiology, biotechnologies, bioinformatics and plant genomic resources.
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