黄酮类化合物诱导紫菀属跨种抗虫活性

IF 3.6 2区 生物学 Q1 PLANT SCIENCES
Li-Jun Zhang, Xin-You Wang, Ying Liu, Yan-Long Wang, Yu-Shou Ma
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引用次数: 0

摘要

高海拔(平均3753 m)三江源地区的开花紫菀(Aster spp.)物种经常受到浅喉炎(Tephritis angustipennis)的破坏,对其生存和生产力造成严重的负面影响。研究表明,害虫胁迫提高了紫菀花抗氧化酶活性(CAT、POD、SOD和PPO),增加了次生代谢产物,尤其是黄酮类化合物。综合转录组学和代谢组学分析确定了三个紫菀品种之间的差异反应,表现出不同的抗性水平。我们发现,害虫胁迫的增加,特别是在严重危害(HH)条件下,会上调抗性相关基因,促进酚类和萜类化合物的积累。害虫取食激活了类黄酮生物合成途径,关键酶基因(PAL、CAD、HCT、FLS和CYP)上调,反映出快速的生理反应,增强了抗性。值得注意的是,黄酮类化合物的合成在应激反应中受到动态调节。在HH条件下,槲皮素和山奈酚水平降低,而苯丙素、山奈素、樱素和异樱素水平升高,表明其防御策略复杂。总的来说,害虫诱导的类黄酮积累有助于延缓花的老化和变质过程,从而提高种子产量。这些发现为紫菀属植物的分子防御机制提供了有价值的见解,为选育抗虫品种和制定有效的害虫防治策略提供了潜在的靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tephritis Angustipennis-Induced Flavonoid Dynamics Drive Cross-Species Pest Resistance in Aster spp.

Flowering Aster species (Aster spp.) native to the high-altitude (3753 m on average) Three Rivers Source Region are frequently damaged by Tephritis angustipennis, imposing significant stress that negatively impacts their survival and productivity. This study reveals that pest stress enhances antioxidant enzyme activity (CAT, POD, SOD, and PPO) and increases secondary metabolites, particularly flavonoids, in Aster flowers. Integrated transcriptomic and metabolomic analyses identified differential responses among three Aster varieties exhibiting distinct resistance levels. We found that increasing pest stress, particularly under serious-hazard (HH) conditions, upregulates resistance-related genes and promotes the accumulation of phenolic and terpenoid compounds. Pest feeding activates the flavonoid biosynthesis pathway, with key enzyme genes (PAL, CAD, HCT, FLS, and CYP) being upregulated, reflecting a rapid physiological response that enhances resistance. Notably, flavonoid synthesis is dynamically regulated in response to stress. Under HH conditions, quercetin and kaempferol levels decrease, while phlorizin, kaempferide, sakuranetin, and isosakuranetin increase, indicating a complex defense strategy. Overall, pest-induced flavonoid accumulation helps delay the process of flower aging and deterioration, thereby enhancing seed yield. These findings provide valuable insights into the molecular defense mechanisms of Aster spp., offering potential targets for breeding pest-resistant varieties and developing effective pest management strategies.

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来源期刊
Physiologia plantarum
Physiologia plantarum 生物-植物科学
CiteScore
11.00
自引率
3.10%
发文量
224
审稿时长
3.9 months
期刊介绍: Physiologia Plantarum is an international journal committed to publishing the best full-length original research papers that advance our understanding of primary mechanisms of plant development, growth and productivity as well as plant interactions with the biotic and abiotic environment. All organisational levels of experimental plant biology – from molecular and cell biology, biochemistry and biophysics to ecophysiology and global change biology – fall within the scope of the journal. The content is distributed between 5 main subject areas supervised by Subject Editors specialised in the respective domain: (1) biochemistry and metabolism, (2) ecophysiology, stress and adaptation, (3) uptake, transport and assimilation, (4) development, growth and differentiation, (5) photobiology and photosynthesis.
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