Harnessing drought-induced immune priming for intergenerational resistance to spot blotch in wheat

IF 3.3 3区 农林科学 Q2 PLANT SCIENCES Physiological and Molecular Plant Pathology Pub Date : 2025-03-01 Epub Date: 2024-12-30 DOI:10.1016/j.pmpp.2024.102558
Bandana Devi , Nidhi Yadav , Menka Tiwari, Shweta Gupta, Bhumika Chhodvadiya, Prashant Singh
{"title":"Harnessing drought-induced immune priming for intergenerational resistance to spot blotch in wheat","authors":"Bandana Devi ,&nbsp;Nidhi Yadav ,&nbsp;Menka Tiwari,&nbsp;Shweta Gupta,&nbsp;Bhumika Chhodvadiya,&nbsp;Prashant Singh","doi":"10.1016/j.pmpp.2024.102558","DOIUrl":null,"url":null,"abstract":"<div><div>Drought priming has proven to be an effective strategy in modern agriculture for enhancing crop resistance to pathogens. However, the biochemical and metabolic mechanisms underlying these protective effects under biotic stress remain insufficiently understood, offering a valuable opportunity for further research. This study demonstrates that drought-induced priming in wheat (<em>Triticum aestivum</em>) not only improves resistance to <em>Bipolaris sorokiniana</em> (spot blotch) but also transfers this protection to the subsequent generation (G1). Using growth metrics, disease assessments, biochemical analysis, and yield evaluations, we found that progeny of drought-primed plants showed enhanced defense responses under pathogen stress, despite no morphological differences in stress-free conditions. Significant increases in photosynthetic pigments-chlorophyll a (3.80-fold), chlorophyll <em>b</em> (3.27-fold), and carotenoids (2.69-fold) were observed, along with key stress markers like proline (1.78-fold), total phenolics (1.30-fold), and ascorbic acid (2.30-fold). The progeny also exhibited an 8.37-fold reduction in malondialdehyde (MDA) levels, indicating reduced oxidative damage. Under biotic stress, drought-primed progeny displayed increased activities of antioxidant enzymes, including superoxide dismutase (2.35-fold), catalase (2.48-fold), and ascorbate peroxidase (3.37-fold), along with upregulated defense enzymes like peroxidase (1.44-fold), phenylalanine ammonia-lyase (1.97-fold) and chitinase (1.88-fold). These biochemical adjustments optimized resource allocation for both growth and defense. Additionally, drought-primed progeny showed improved yield performance compared to non-primed progeny under stress.</div><div>Our findings highlight drought-induced intergenerational priming as a sustainable, chemical-free strategy for long-term crop protection, offering a path toward resilient crop varieties in the face of global climate challenges.</div></div>","PeriodicalId":20046,"journal":{"name":"Physiological and Molecular Plant Pathology","volume":"136 ","pages":"Article 102558"},"PeriodicalIF":3.3000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physiological and Molecular Plant Pathology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0885576524003424","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/12/30 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Drought priming has proven to be an effective strategy in modern agriculture for enhancing crop resistance to pathogens. However, the biochemical and metabolic mechanisms underlying these protective effects under biotic stress remain insufficiently understood, offering a valuable opportunity for further research. This study demonstrates that drought-induced priming in wheat (Triticum aestivum) not only improves resistance to Bipolaris sorokiniana (spot blotch) but also transfers this protection to the subsequent generation (G1). Using growth metrics, disease assessments, biochemical analysis, and yield evaluations, we found that progeny of drought-primed plants showed enhanced defense responses under pathogen stress, despite no morphological differences in stress-free conditions. Significant increases in photosynthetic pigments-chlorophyll a (3.80-fold), chlorophyll b (3.27-fold), and carotenoids (2.69-fold) were observed, along with key stress markers like proline (1.78-fold), total phenolics (1.30-fold), and ascorbic acid (2.30-fold). The progeny also exhibited an 8.37-fold reduction in malondialdehyde (MDA) levels, indicating reduced oxidative damage. Under biotic stress, drought-primed progeny displayed increased activities of antioxidant enzymes, including superoxide dismutase (2.35-fold), catalase (2.48-fold), and ascorbate peroxidase (3.37-fold), along with upregulated defense enzymes like peroxidase (1.44-fold), phenylalanine ammonia-lyase (1.97-fold) and chitinase (1.88-fold). These biochemical adjustments optimized resource allocation for both growth and defense. Additionally, drought-primed progeny showed improved yield performance compared to non-primed progeny under stress.
Our findings highlight drought-induced intergenerational priming as a sustainable, chemical-free strategy for long-term crop protection, offering a path toward resilient crop varieties in the face of global climate challenges.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
利用干旱诱导免疫启动对小麦斑病的代际抗性
干旱启动是现代农业中提高作物抗病性的有效策略。然而,生物胁迫下这些保护作用背后的生化和代谢机制尚不清楚,这为进一步研究提供了宝贵的机会。本研究表明,干旱诱导的小麦(Triticum aestivum)引种不仅提高了小麦对斑点病(Bipolaris sorokiniana)的抗性,而且还将这种保护作用传递给下一代(G1)。通过生长指标、病害评估、生化分析和产量评估,我们发现干旱植物的后代在病原体胁迫下表现出增强的防御反应,尽管在无胁迫条件下没有形态差异。光合色素——叶绿素a(3.80倍)、叶绿素b(3.27倍)和类胡萝卜素(2.69倍)显著增加,以及脯氨酸(1.78倍)、总酚类物质(1.30倍)和抗坏血酸(2.30倍)等关键应激标志物也显著增加。后代丙二醛(MDA)水平也降低了8.37倍,表明氧化损伤减少。在生物胁迫下,干旱引发的后代抗氧化酶活性增加,包括超氧化物歧化酶(2.35倍)、过氧化氢酶(2.48倍)和抗坏血酸过氧化物酶(3.37倍),防御酶如过氧化物酶(1.44倍)、苯丙氨酸解氨酶(1.97倍)和几丁质酶(1.88倍)。这些生化调整优化了生长和防御的资源配置。此外,干旱处理后代在胁迫下的产量表现优于未处理后代。我们的研究结果强调,干旱诱导的代际启动是一种可持续的、无化学物质的长期作物保护策略,为面对全球气候挑战的作物品种提供了一条道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
4.30
自引率
7.40%
发文量
130
审稿时长
38 days
期刊介绍: Physiological and Molecular Plant Pathology provides an International forum for original research papers, reviews, and commentaries on all aspects of the molecular biology, biochemistry, physiology, histology and cytology, genetics and evolution of plant-microbe interactions. Papers on all kinds of infective pathogen, including viruses, prokaryotes, fungi, and nematodes, as well as mutualistic organisms such as Rhizobium and mycorrhyzal fungi, are acceptable as long as they have a bearing on the interaction between pathogen and plant.
期刊最新文献
Biocontrol potential of Trichoderma culture filtrates against Schizophyllum commune: Metabolite profiling and oxidative stress mechanisms Soybean isoflavones as dual-action natural agents that prime host immunity and suppress Pseudomonas virulence Antifungal activity and mechanism of ethanol extract from Stellera chamaejasme against Pestalotiopsis neglecta — A basis for the development of potential botanical fungicides Biological and molecular characterization of Potyvirus rapae infecting chrysanthemum in Thailand Isolation and identification of two causal agents associated with root rot of Scutellaria baicalensis
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1