Abid Hussain Wani, Irfan Rashid, Rayees Ahmad Rather, Riffat John
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Resistant genotypes showed higher Si concentrations than susceptible ones, leading to the selection of two contrasting genotypes, <em>viz</em>., WW-120 (resistant) and K-88 (susceptible), for further analysis. In these genotypes, the expression of Si transporters and various physiological and biochemical responses were studied under stripe rust infestation with and without Si supplementation. We found that Si supplementation upregulated the expression of Si transporters, with a more pronounced increase in the resistant genotype than in the susceptible one, resulting in higher Si accumulation in the former. Moreover, differential physiological and biochemical responses to rust infection and Si supplementation were observed in both genotypes, indicating genotype-dependent variations across all measured variables. Our results suggest that higher Si accumulation in resistant wheat genotypes, due to the upregulation of Si transporters, plays a crucial role in their defense against rust infection. 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引用次数: 0
摘要
众所周知,补充硅(Si)有助于植物减轻各种生物和非生物胁迫。然而,人们对硅介导的胁迫缓解机制,特别是硅转运体的参与和基因型特异性反应仍知之甚少。在此背景下,我们研究了硅转运体在感染条锈病的特定小麦基因型中缓解生物胁迫的作用。主要目的是评估不同小麦基因型在条锈病抗性中的硅积累作用,并确定硅转运体如何影响其抗性反应。对 20 个小麦基因型在芽中积累硅的能力进行了评估,结果显示所选基因型之间存在显著差异。抗性基因型比易感基因型表现出更高的硅浓度,因此选择了两个对比基因型,即 WW-120(抗性)和 K-88(易感)进行进一步分析。在补充和不补充 Si 的情况下,研究了这些基因型在条锈病侵染下 Si 转运体的表达以及各种生理生化反应。我们发现,补硅会上调硅转运体的表达,抗性基因型比易感基因型的表达量增加得更明显,导致前者的硅积累量更高。此外,两种基因型对锈病感染和补硅都有不同的生理生化反应,这表明所有测量变量的变化都取决于基因型。我们的研究结果表明,由于硅转运体的上调,抗性小麦基因型中较高的硅积累在其抵御锈病感染的过程中发挥了关键作用。进一步阐明这些机制可用于通过有针对性的硅管理增强植物对生物胁迫的抵抗力。
Transporters regulate silicon uptake to make stripe rust resistant wheat genotypes more effective
Silicon (Si) supplementation is known to aid plants in mitigating various biotic and abiotic stressors. However, the mechanisms underlying Si-mediated stress alleviation, particularly the involvement of Si transporters and genotype-specific responses, remain poorly understood. Against this backdrop, we investigated the role of Si transporters in biotic stress alleviation in specific wheat genotypes infected with stripe rust. The primary objectives were to assess the role of Si accumulation in stripe rust resistance across different wheat genotypes and to determine how Si transporters affect their resistance responses. Twenty wheat genotypes were evaluated for their ability to accumulate Si in shoots, revealing significant variations among the selected genotypes. Resistant genotypes showed higher Si concentrations than susceptible ones, leading to the selection of two contrasting genotypes, viz., WW-120 (resistant) and K-88 (susceptible), for further analysis. In these genotypes, the expression of Si transporters and various physiological and biochemical responses were studied under stripe rust infestation with and without Si supplementation. We found that Si supplementation upregulated the expression of Si transporters, with a more pronounced increase in the resistant genotype than in the susceptible one, resulting in higher Si accumulation in the former. Moreover, differential physiological and biochemical responses to rust infection and Si supplementation were observed in both genotypes, indicating genotype-dependent variations across all measured variables. Our results suggest that higher Si accumulation in resistant wheat genotypes, due to the upregulation of Si transporters, plays a crucial role in their defense against rust infection. Further elucidation of these mechanisms could be used to enhance plant resistance to biotic stressors through targeted Si management.
期刊介绍:
Plant Physiology and Biochemistry publishes original theoretical, experimental and technical contributions in the various fields of plant physiology (biochemistry, physiology, structure, genetics, plant-microbe interactions, etc.) at diverse levels of integration (molecular, subcellular, cellular, organ, whole plant, environmental). Opinions expressed in the journal are the sole responsibility of the authors and publication does not imply the editors'' agreement.
Manuscripts describing molecular-genetic and/or gene expression data that are not integrated with biochemical analysis and/or actual measurements of plant physiological processes are not suitable for PPB. Also "Omics" studies (transcriptomics, proteomics, metabolomics, etc.) reporting descriptive analysis without an element of functional validation assays, will not be considered. Similarly, applied agronomic or phytochemical studies that generate no new, fundamental insights in plant physiological and/or biochemical processes are not suitable for publication in PPB.
Plant Physiology and Biochemistry publishes several types of articles: Reviews, Papers and Short Papers. Articles for Reviews are either invited by the editor or proposed by the authors for the editor''s prior agreement. Reviews should not exceed 40 typewritten pages and Short Papers no more than approximately 8 typewritten pages. The fundamental character of Plant Physiology and Biochemistry remains that of a journal for original results.