Plant defense against insect herbivory: Flavonoid-mediated growth inhibition of Helicoverpa zea

IF 6.8 Q1 PLANT SCIENCES Plant Stress Pub Date : 2025-03-01 Epub Date: 2025-01-03 DOI:10.1016/j.stress.2025.100738
Debamalya Chatterjee , Charles Colvin , Tyler Lesko , Michelle Peiffer , Gary W. Felton , Surinder Chopra
{"title":"Plant defense against insect herbivory: Flavonoid-mediated growth inhibition of Helicoverpa zea","authors":"Debamalya Chatterjee ,&nbsp;Charles Colvin ,&nbsp;Tyler Lesko ,&nbsp;Michelle Peiffer ,&nbsp;Gary W. Felton ,&nbsp;Surinder Chopra","doi":"10.1016/j.stress.2025.100738","DOIUrl":null,"url":null,"abstract":"<div><div>Plant biotic stressors, including insect damage to economically important crops, are on the rise because of climate change (Skendžić et al., 2021; Matzrafi, 2019; Hatfield et al., 2011). Corn earworm (CEW) <em>Helicoverpa zea</em> (Boddie) is one of the economically important insect pests of maize (<em>Zea mays</em> L.) and sorghum (<em>Sorghum bicolor</em> (L.) Moench). In this study, maize near-isogenic lines with high flavonoid content in silks, husks, and kernel pericarps were used to test against the survival of CEW larvae. Larvae feeding on high-flavonoid maize lines had increased mortality and reduced body weight. These larvae showed leakage of the midgut peritrophic matrix, indicating leaky-gut-like syndrome suggesting involvement of microbiome changes in the larval gut. Moreover, the expression of chitin formation and gut health-related genes was changed in the midgut of larvae consuming the flavonoid-rich husks. CEW herbivory caused high and localized accumulation of flavonols around the damaged husk area. Silks and husks of high flavonoid lines also had elevated levels of 3-deoxyanthocyanidins (3-DAs) and flavan-4-ols, which contributed to increased larval mortality. Feeding assays using an artificial diet supplemented with a sorghum 3-DAs-rich extract further confirmed the efficacy of these flavonoids in increasing larval mortality. Altogether, this study suggests a novel option for integrated pest management for CEW larvae.</div></div>","PeriodicalId":34736,"journal":{"name":"Plant Stress","volume":"15 ","pages":"Article 100738"},"PeriodicalIF":6.8000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Stress","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667064X2500003X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/3 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Plant biotic stressors, including insect damage to economically important crops, are on the rise because of climate change (Skendžić et al., 2021; Matzrafi, 2019; Hatfield et al., 2011). Corn earworm (CEW) Helicoverpa zea (Boddie) is one of the economically important insect pests of maize (Zea mays L.) and sorghum (Sorghum bicolor (L.) Moench). In this study, maize near-isogenic lines with high flavonoid content in silks, husks, and kernel pericarps were used to test against the survival of CEW larvae. Larvae feeding on high-flavonoid maize lines had increased mortality and reduced body weight. These larvae showed leakage of the midgut peritrophic matrix, indicating leaky-gut-like syndrome suggesting involvement of microbiome changes in the larval gut. Moreover, the expression of chitin formation and gut health-related genes was changed in the midgut of larvae consuming the flavonoid-rich husks. CEW herbivory caused high and localized accumulation of flavonols around the damaged husk area. Silks and husks of high flavonoid lines also had elevated levels of 3-deoxyanthocyanidins (3-DAs) and flavan-4-ols, which contributed to increased larval mortality. Feeding assays using an artificial diet supplemented with a sorghum 3-DAs-rich extract further confirmed the efficacy of these flavonoids in increasing larval mortality. Altogether, this study suggests a novel option for integrated pest management for CEW larvae.
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
植物对草食昆虫的防御:黄酮类介导的玉米螺旋虫生长抑制
由于气候变化,包括昆虫对重要经济作物的损害在内的植物生物胁迫源正在增加(Skendžić等人,2021;Matzrafi, 2019;Hatfield et al., 2011)。玉米耳虫是玉米(zea mays L.)和高粱(sorghum bicolor (L.))的重要经济害虫之一。Moench)。本研究采用玉米蚕丝、谷壳和果皮黄酮含量高的近等基因系对CEW幼虫的存活进行了试验。饲喂高黄酮玉米品系的幼虫死亡率增加,体重减轻。这些幼虫显示出中肠营养基质的渗漏,表明肠道渗漏样综合征,表明幼虫肠道微生物群的变化。此外,在食用富含类黄酮的壳的幼虫中肠中,几丁质形成和肠道相关基因的表达发生了变化。草食导致黄酮类醇在受损果皮周围大量和局部积累。高类黄酮品系的蚕丝和壳中3-脱氧花青素(3-DAs)和黄烷-4-醇含量也较高,这是导致幼虫死亡率升高的原因之一。在人工饲料中添加富含3- das的高粱提取物,进一步证实了黄酮类化合物对提高幼虫死亡率的作用。总之,本研究提出了一种新的害虫综合管理方法。
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
Plant Stress
Plant Stress PLANT SCIENCES-
CiteScore
5.20
自引率
8.00%
发文量
76
审稿时长
63 days
期刊介绍: The journal Plant Stress deals with plant (or other photoautotrophs, such as algae, cyanobacteria and lichens) responses to abiotic and biotic stress factors that can result in limited growth and productivity. Such responses can be analyzed and described at a physiological, biochemical and molecular level. Experimental approaches/technologies aiming to improve growth and productivity with a potential for downstream validation under stress conditions will also be considered. Both fundamental and applied research manuscripts are welcome, provided that clear mechanistic hypotheses are made and descriptive approaches are avoided. In addition, high-quality review articles will also be considered, provided they follow a critical approach and stimulate thought for future research avenues. Plant Stress welcomes high-quality manuscripts related (but not limited) to interactions between plants and: Lack of water (drought) and excess (flooding), Salinity stress, Elevated temperature and/or low temperature (chilling and freezing), Hypoxia and/or anoxia, Mineral nutrient excess and/or deficiency, Heavy metals and/or metalloids, Plant priming (chemical, biological, physiological, nanomaterial, biostimulant) approaches for improved stress protection, Viral, phytoplasma, bacterial and fungal plant-pathogen interactions. The journal welcomes basic and applied research articles, as well as review articles and short communications. All submitted manuscripts will be subject to a thorough peer-reviewing process.
期刊最新文献
Metabolic biomarker-based phenotyping unveils quantitative effects of plant resistance and pathogen aggressiveness in the grapevine (Vitis spp.) - downy mildew (Plasmopara viticola) pathosystem Drought effects on the leaf uptake of carbonyl sulfide and CO₂ in Pinus sylvestris and Juniperus communis OsLOX9 confers thermotolerance in rice via JA-mediated enhancement of antioxidant defense DUF538-domain proteins SVB and SVB2 act as positive regulators of ABA and salt stress responses in Arabidopsis Integrated physiological, biochemical, and molecular analysis of Populus alba “Villafranca” under salinity stress
×
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