Succulence and aquaporin expression during drought and recovery in the CAM epiphytic bromeliad Acanthostachys strobilacea (Schult. & Schult.f.) Klotzsch

IF 4.5 2区 生物学 Q2 ENVIRONMENTAL SCIENCES Environmental and Experimental Botany Pub Date : 2024-09-25 DOI:10.1016/j.envexpbot.2024.105985
Victória Carvalho , Evandro Alves Vieira , Kleber Resende Silva , Eduardo Purgatto , Catarina Carvalho Nievola , Marília Gaspar
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Abstract

Due to climate change, drought-rewatering cycles might become more intense and frequent, potentially threatening epiphytic bromeliads as they are detached from the soil. Hence, research on drought-rewatering responses is essential to determine the resilience of these species to projected future environmental conditions. The tankless, CAM epiphytic bromeliad Acanthostachys strobilacea shows significant drought tolerance from its early developmental stages. Here, we investigated water storage remobilization and the expression of aquaporin genes in the succulent leaf tissues of juvenile A. strobilacea plants in response to a drought-rewatering cycle and their relation to metabolic status. Under greenhouse conditions, 3-month-old plants were subjected to 14 days without irrigation, followed by 1 day of rewatering. We conducted analyses of water status, leaf anatomy, photosynthetic rates, titratable acidity, metabolic profile, and aquaporin gene expression. Data on water status indicated drought-induced turgor loss, which could be mainly attributed to the collapse of the hydrenchyma (water-storage tissue). The water stored in these cells likely relocated to the photosynthetically active cells of the chlorenchyma, which may have helped maintain metabolic activity. Indeed, titratable acidity, gas exchange, and metabolic data showed intensified CAM activity after drought. Drought also increased proline and antioxidant contents but significantly reduced the expression of AsPIP1;1, AsPIP1;2-like, AsTIP2;2 and AsNIP2;2 genes. After 1 day of rewatering, turgor, CAM activity, and the expression of most aquaporin genes and most metabolite contents were fully restored to control levels. The rapid turgor recovery, even in the absence of leaf water-absorbing trichomes, was due to water storage in hydrenchyma cells upon rehydration. Additionally, the modulation of aquaporin expression likely reduced water loss during drought and aided turgor restoration after rewatering. These results can guide future research on the responses of epiphytic bromeliads to climate change, essential to developing conservation strategies.
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CAM附生凤梨Acanthostachys strobilacea (Schult. & Schult.f.) Klotzsch在干旱和恢复期间的萌发和水气素表达
由于气候变化,干旱-抽水周期可能会变得更加剧烈和频繁,从而对脱离土壤的附生凤梨造成潜在威胁。因此,对干旱-反水反应的研究对于确定这些物种对未来环境条件的适应能力至关重要。无水箱、CAM附生凤梨Acanthostachys strobilacea在其早期发育阶段就表现出明显的耐旱性。在此,我们研究了石莲花幼株肉质叶组织在干旱-再浇水循环中的储水再动员和水蒸素基因的表达及其与代谢状态的关系。在温室条件下,3 个月大的植株在没有灌溉的情况下生长了 14 天,然后重新灌溉 1 天。我们对水分状况、叶片解剖结构、光合速率、可滴定酸度、新陈代谢状况和水气素基因表达进行了分析。有关水分状态的数据表明,干旱会导致水分流失,这主要是由于水分沟(储水组织)塌陷造成的。这些细胞中储存的水分可能转移到了具有光合作用的脉络膜细胞中,这可能有助于维持新陈代谢活动。事实上,可滴定酸度、气体交换和新陈代谢数据都表明,干旱后 CAM 的活性增强了。干旱还增加了脯氨酸和抗氧化剂的含量,但显著降低了 AsPIP1;1、AsPIP1;2-like、AsTIP2;2 和 AsNIP2;2 基因的表达。重新浇水 1 天后,水分、CAM 活性、大多数水蒸气素基因的表达和大多数代谢物的含量完全恢复到对照水平。即使在没有叶片吸水毛状体的情况下,水分也能迅速恢复,这是因为补水后水分储存在水沟细胞中。此外,调节水蒸发蛋白的表达可能减少了干旱期间的水分损失,并有助于重新灌水后的水分恢复。这些结果可以指导未来关于附生凤梨对气候变化的反应的研究,对制定保护策略至关重要。
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来源期刊
Environmental and Experimental Botany
Environmental and Experimental Botany 环境科学-环境科学
CiteScore
9.30
自引率
5.30%
发文量
342
审稿时长
26 days
期刊介绍: Environmental and Experimental Botany (EEB) publishes research papers on the physical, chemical, biological, molecular mechanisms and processes involved in the responses of plants to their environment. In addition to research papers, the journal includes review articles. Submission is in agreement with the Editors-in-Chief. The Journal also publishes special issues which are built by invited guest editors and are related to the main themes of EEB. The areas covered by the Journal include: (1) Responses of plants to heavy metals and pollutants (2) Plant/water interactions (salinity, drought, flooding) (3) Responses of plants to radiations ranging from UV-B to infrared (4) Plant/atmosphere relations (ozone, CO2 , temperature) (5) Global change impacts on plant ecophysiology (6) Biotic interactions involving environmental factors.
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