Global climate warming has significantly increased plant diseases prevalence. In subtropical regions, high temperature frequently co-occurs with bacterial wilt caused by Ralstonia solanacearum, creating compound stress conditions that severely compromise eggplant productivity. However, the molecular mechanisms governing eggplant's response to combined heat and pathogen stress remain poorly characterized. In this study, we conducted the temperature analyses of Guangzhou, China, and isolated a thermotolerant strain PSS219-GZ under high temperatures in eggplant. Phenotypic analysis of eggplants inoculated with PSS219-GZ at different temperature, indicated that PSS219-GZ have maximal pathogenicity at 37°C. SmWRKY6 is a WRKY transcription factor activated by both high temperatures and Ralstonia solanacearum infection. Genetic evidence from silencing of SmWRKY6 via VIGS in eggplants and overexpression of SmWRKY6 in tomato demonstrated that SmWRKY6 is essential for enhancing resistance to Ralstonia solanacearum under high-temperature stress. SmWRKY6 directly binds to and transcriptionally activates the SmPR1b promoter, forming a key regulatory node in bacterial wilt resistance pathways. This study provides novel insights into plant responses to combined heat and R. solanacearum stress and highlights potential resistance genes for mitigating compound stress effects.
{"title":"SmWRKY6 Mediates Thermo-Enhanced Resistance to Ralstonia solanacearum in Eggplant by Activating SmPR1b.","authors":"Yonggui Liang, Bingwei Yu, Renjian Liu, Zhilei Xia, Liping Chen, Zhengkun Qiu, Shuangshuang Yan, Bihao Cao","doi":"10.1111/pce.70360","DOIUrl":"https://doi.org/10.1111/pce.70360","url":null,"abstract":"<p><p>Global climate warming has significantly increased plant diseases prevalence. In subtropical regions, high temperature frequently co-occurs with bacterial wilt caused by Ralstonia solanacearum, creating compound stress conditions that severely compromise eggplant productivity. However, the molecular mechanisms governing eggplant's response to combined heat and pathogen stress remain poorly characterized. In this study, we conducted the temperature analyses of Guangzhou, China, and isolated a thermotolerant strain PSS219-GZ under high temperatures in eggplant. Phenotypic analysis of eggplants inoculated with PSS219-GZ at different temperature, indicated that PSS219-GZ have maximal pathogenicity at 37°C. SmWRKY6 is a WRKY transcription factor activated by both high temperatures and Ralstonia solanacearum infection. Genetic evidence from silencing of SmWRKY6 via VIGS in eggplants and overexpression of SmWRKY6 in tomato demonstrated that SmWRKY6 is essential for enhancing resistance to Ralstonia solanacearum under high-temperature stress. SmWRKY6 directly binds to and transcriptionally activates the SmPR1b promoter, forming a key regulatory node in bacterial wilt resistance pathways. This study provides novel insights into plant responses to combined heat and R. solanacearum stress and highlights potential resistance genes for mitigating compound stress effects.</p>","PeriodicalId":222,"journal":{"name":"Plant, Cell & Environment","volume":" ","pages":""},"PeriodicalIF":6.3,"publicationDate":"2025-12-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145852712","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Common mycorrhizal networks (CMN) formed by arbuscular mycorrhizal (AM) fungi are critical pathways for plant nutrition and interplant nutrient transfer. However, their role in mediating sexually asymmetric interactions in dioecious plants remains poorly understood, especially under nitrogen (N) deficiency. Using in vivo 15N leaf-labeling in Populus cathayana saplings, we quantified N transfer via CMN between sexes and linked them to root traits. We found that intersexual pairs facilitated CMN-mediated N transfer from male to female saplings; this transfer was markedly amplified under low N conditions. When N availability shifted from sufficient to deficient conditions, males shifted from a conservative strategy to an AM fungi-dependent 'outsourcing' strategy (characterized by higher mycorrhizal colonization rates), whereas females transitioned from a relatively weak root foraging strategy to an enhanced one (with greater specific root length and specific root area). This strategic divergence promoted sexually asymmetric N transfer via CMN, leading to optimized nutrient use efficiency at the population level. These results highlighted a previously unrecognized role of CMN in facilitating sexually asymmetric nutrient interactions, offering a mechanistic framework to improve both productivity and sustainability in dioecious plantations on nutrient-poor soils.
{"title":"Sex-Specific Root Strategies Drive Asymmetric Nitrogen Transfer via Common Mycorrhizal Networks Under Nitrogen Deficiency in Populus cathayana.","authors":"Wentong Gao, El-Hadji Malick Cisse, Yaseen Khan, Dadong Li, Xiao Xu","doi":"10.1111/pce.70346","DOIUrl":"https://doi.org/10.1111/pce.70346","url":null,"abstract":"<p><p>Common mycorrhizal networks (CMN) formed by arbuscular mycorrhizal (AM) fungi are critical pathways for plant nutrition and interplant nutrient transfer. However, their role in mediating sexually asymmetric interactions in dioecious plants remains poorly understood, especially under nitrogen (N) deficiency. Using in vivo <sup>15</sup>N leaf-labeling in Populus cathayana saplings, we quantified N transfer via CMN between sexes and linked them to root traits. We found that intersexual pairs facilitated CMN-mediated N transfer from male to female saplings; this transfer was markedly amplified under low N conditions. When N availability shifted from sufficient to deficient conditions, males shifted from a conservative strategy to an AM fungi-dependent 'outsourcing' strategy (characterized by higher mycorrhizal colonization rates), whereas females transitioned from a relatively weak root foraging strategy to an enhanced one (with greater specific root length and specific root area). This strategic divergence promoted sexually asymmetric N transfer via CMN, leading to optimized nutrient use efficiency at the population level. These results highlighted a previously unrecognized role of CMN in facilitating sexually asymmetric nutrient interactions, offering a mechanistic framework to improve both productivity and sustainability in dioecious plantations on nutrient-poor soils.</p>","PeriodicalId":222,"journal":{"name":"Plant, Cell & Environment","volume":" ","pages":""},"PeriodicalIF":6.3,"publicationDate":"2025-12-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145848481","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Xi Chen, Shiyu Han, Xiujuan Wang, Hannah Rae Thomas, Yanhong Zhou, Huijia Kang
As the primary energy source for photosynthesis, light also serves as a critical environmental cue regulating developmental plasticity through photomorphogenesis. While extensive research has characterized light-mediated shoot development, including hypocotyl de-etiolation, cotyledon expansion and chloroplast biogenesis, emerging evidence demonstrates that light signals also profoundly influence the root. Phenotypic analyses of photoreceptor mutants have revealed that roots, like above-ground tissues, perceive and respond to light signals through sophisticated signalling networks. This review synthesizes current understanding of core light signalling cascades and the systemic mechanisms facilitating shoot-to-root signal transmission. We highlight recent advances in understanding how light quality and intensity modulate root development through hormonal crosstalk and transcriptional reprogramming. By integrating molecular mechanisms with agronomic applications, we further provide a detailed summary of the application of plant photobiology. It suggests practical strategies for optimizing root development through light-mediated control.
{"title":"Molecular Mechanisms of Light Signalling in Root Architecture: From Photoreception to Developmental Regulation.","authors":"Xi Chen, Shiyu Han, Xiujuan Wang, Hannah Rae Thomas, Yanhong Zhou, Huijia Kang","doi":"10.1111/pce.70350","DOIUrl":"10.1111/pce.70350","url":null,"abstract":"<p><p>As the primary energy source for photosynthesis, light also serves as a critical environmental cue regulating developmental plasticity through photomorphogenesis. While extensive research has characterized light-mediated shoot development, including hypocotyl de-etiolation, cotyledon expansion and chloroplast biogenesis, emerging evidence demonstrates that light signals also profoundly influence the root. Phenotypic analyses of photoreceptor mutants have revealed that roots, like above-ground tissues, perceive and respond to light signals through sophisticated signalling networks. This review synthesizes current understanding of core light signalling cascades and the systemic mechanisms facilitating shoot-to-root signal transmission. We highlight recent advances in understanding how light quality and intensity modulate root development through hormonal crosstalk and transcriptional reprogramming. By integrating molecular mechanisms with agronomic applications, we further provide a detailed summary of the application of plant photobiology. It suggests practical strategies for optimizing root development through light-mediated control.</p>","PeriodicalId":222,"journal":{"name":"Plant, Cell & Environment","volume":" ","pages":""},"PeriodicalIF":6.3,"publicationDate":"2025-12-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145852694","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Yang Yang, Jia Wang, Fuchuan Han, Jiantao Zhang, Beiping Liu, Ming Gao, Yunxiao Zhao, Yicun Chen, Yangdong Wang
Plant uridine diphosphate-dependent glycosyltransferases (UGTs) play a key role in plant growth and defense mechanisms. Tung oil tree (Vernicia fordii), suffers from disease caused by Fusarium oxysporum f. sp. Fordiis (Fol). However, little is known about how to enhance the resistance mechanism. In this study, we observed significant enrichment of flavonoid biosynthesis pathway in V. fordii roots following Fol infection, including myricetin-glucoside and kaempferol-glucoside. Based on transcriptomic analysis, we screened 11VfUGTs showing elevated expression in response to Fol infection. Through correlation analysis (Pearson's r) between flavonoid metabolite level and 11VfUGTs transcription levels, we discovered that increased flavonol glycoside accumulation post-infection was associated with VfUGT87H9 activity. Furthermore, the VfUGT87H9 gene exhibited strong root-specific expression and rapid transcriptional induction upon Fol challenge. In vitro enzymatic assays confirmed VfUGT87H9's ability to catalyze myricetin glucosylation, producing myricetin-glucoside. Transgenic plants overexpressing VfUGT87H9 demonstrated enhanced pathogen resistance compared to control plants, with OE-VfUGT87H9 roots accumulating significantly higher myricetin-glucoside level. In vitro assays showed that myricetin-glu inhibits mycelial growth and host infection by Fol. Our findings established VfUGT87H9 as a flavonoid glucosyltransferase that positively regulates plant disease resistance by maintaining flavonol glycosides homeostasis. This study advances our understanding of flavonoid-mediated plant-pathogen interactions and metabolic defense strategies.
植物尿苷二磷酸依赖糖基转移酶(UGTs)在植物生长和防御机制中起着关键作用。桐油树(Vernicia fordii)遭受由Fusarium oxysporum f. sp. Fordiis (Fol)引起的疾病。然而,如何增强抗性机制尚不清楚。在本研究中,我们观察到紫花苜蓿感染后,紫花苜蓿根部黄酮类生物合成途径,包括杨梅苷-葡萄糖苷和山奈酚-葡萄糖苷显著富集。基于转录组学分析,我们筛选了11VfUGTs,在Fol感染反应中表达升高。通过类黄酮代谢物水平与11VfUGTs转录水平的相关分析(Pearson’s r),我们发现感染后黄酮醇苷积累增加与VfUGT87H9活性相关。此外,VfUGT87H9基因在Fol刺激下表现出强烈的根特异性表达和快速的转录诱导。体外酶促实验证实了VfUGT87H9能够催化杨梅素糖基化,生成杨梅素糖苷。与对照植株相比,过表达VfUGT87H9的转基因植株对病原菌的抗性增强,e -VfUGT87H9的根积累的杨梅素-葡萄糖苷水平显著提高。体外实验表明,杨梅素-glu能抑制真菌菌丝生长和宿主感染。我们的研究结果表明,VfUGT87H9是一种黄酮类糖基转移酶,通过维持黄酮醇苷的稳态来积极调节植物的抗病性。这项研究促进了我们对黄酮类化合物介导的植物-病原体相互作用和代谢防御策略的理解。
{"title":"VfUGT87H9 Enhances Fusarium Resistance in Vernicia fordii via Myricetin Glucosylation-Mediated Flavonoid Metabolism.","authors":"Yang Yang, Jia Wang, Fuchuan Han, Jiantao Zhang, Beiping Liu, Ming Gao, Yunxiao Zhao, Yicun Chen, Yangdong Wang","doi":"10.1111/pce.70333","DOIUrl":"https://doi.org/10.1111/pce.70333","url":null,"abstract":"<p><p>Plant uridine diphosphate-dependent glycosyltransferases (UGTs) play a key role in plant growth and defense mechanisms. Tung oil tree (Vernicia fordii), suffers from disease caused by Fusarium oxysporum f. sp. Fordiis (Fol). However, little is known about how to enhance the resistance mechanism. In this study, we observed significant enrichment of flavonoid biosynthesis pathway in V. fordii roots following Fol infection, including myricetin-glucoside and kaempferol-glucoside. Based on transcriptomic analysis, we screened 11VfUGTs showing elevated expression in response to Fol infection. Through correlation analysis (Pearson's r) between flavonoid metabolite level and 11VfUGTs transcription levels, we discovered that increased flavonol glycoside accumulation post-infection was associated with VfUGT87H9 activity. Furthermore, the VfUGT87H9 gene exhibited strong root-specific expression and rapid transcriptional induction upon Fol challenge. In vitro enzymatic assays confirmed VfUGT87H9's ability to catalyze myricetin glucosylation, producing myricetin-glucoside. Transgenic plants overexpressing VfUGT87H9 demonstrated enhanced pathogen resistance compared to control plants, with OE-VfUGT87H9 roots accumulating significantly higher myricetin-glucoside level. In vitro assays showed that myricetin-glu inhibits mycelial growth and host infection by Fol. Our findings established VfUGT87H9 as a flavonoid glucosyltransferase that positively regulates plant disease resistance by maintaining flavonol glycosides homeostasis. This study advances our understanding of flavonoid-mediated plant-pathogen interactions and metabolic defense strategies.</p>","PeriodicalId":222,"journal":{"name":"Plant, Cell & Environment","volume":" ","pages":""},"PeriodicalIF":6.3,"publicationDate":"2025-12-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145848508","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Angel Almagro-Lopez, Micaela Carvajal, Juan Nicolas-Espinosa
{"title":"Evolutionary and Functional Insights Into Aquaporins Genes of Cakile maritima Highlight Their Role in Salinity Adaptation.","authors":"Angel Almagro-Lopez, Micaela Carvajal, Juan Nicolas-Espinosa","doi":"10.1111/pce.70361","DOIUrl":"https://doi.org/10.1111/pce.70361","url":null,"abstract":"","PeriodicalId":222,"journal":{"name":"Plant, Cell & Environment","volume":" ","pages":""},"PeriodicalIF":6.3,"publicationDate":"2025-12-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145848491","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Lian Chen, Changyu Qiu, Gaocong Li, Qiang Lin, Jiehua Chen, Lingyun Sun, Dan Liu, Sen Lin, Dan Wang, Jianan Wu, Zhiyi Li, Yuan Wang, Zhenjiang Wang
This study investigated the mechanisms of cadmium (Cd) tolerance and root exudate-mediated soil activation in mulberry (Morus alba L.), a promising species for phytoremediation. Hydroponic experiments with Cd-tolerant seedlings exposed to 5 and 50 mg/L Cd revealed a biphasic concentration-dependent response. Low Cd induced negligible biological effects, whereas high Cd triggered substantial disturbances across multiple biological levels, including morphological alterations, physiological dysregulation and disrupted elemental accumulation patterns. Metabolomic profiling indicated that Cd stress significantly altered the secretion patterns of 17 root exudate metabolites in mulberry, exemplified by the upregulation of sucrose, lactose and 4-acetylbutyric acid, and the downregulation of β-alanine and myo-inositol. Further pathway enrichment analysis linked these differential metabolites to 17 metabolic pathways, with carbohydrate and amino acid metabolism as the main Cd-responsive pathways, suggesting their core role in mediating mulberry's Cd resistance. Root exudates enhanced soil Cd mobilisation in a positive concentration-dependent yet negative time-dependent manner. Consequently, mulberry adapts to Cd stress via metabolic reprogramming of root exudates-a strategic trade-off that serves a dual role by enhancing plant tolerance while simultaneously increasing Cd bioavailability in the soil. This insight provides a foundational framework for phytoremediation, centred on exudate management and the selection of stress-tolerant varieties.
研究了桑树(Morus alba L.)对镉(Cd)的耐受性和根系分泌物介导的土壤活化机制。对5和50 mg/L Cd的耐Cd幼苗进行水培试验,结果显示出双相浓度依赖性。低Cd诱导的生物效应可以忽略不计,而高Cd则在多个生物水平上引发了实质性的干扰,包括形态改变、生理失调和元素积累模式的破坏。代谢组学分析表明,Cd胁迫显著改变了桑树17种根分泌物代谢物的分泌模式,表现为蔗糖、乳糖和4-乙酰丁酸的分泌上调,β-丙氨酸和肌醇的分泌下调。进一步的途径富集分析将这些差异代谢物与17条代谢途径联系起来,其中碳水化合物和氨基酸代谢是主要的Cd响应途径,表明它们在介导桑树抗Cd的核心作用。根系分泌物对土壤镉的动员具有正向浓度依赖性和负时间依赖性。因此,桑树通过根分泌物的代谢重编程来适应Cd胁迫,这是一种战略性的权衡,在增强植物耐受性的同时增加了土壤中Cd的生物利用度。这一见解为植物修复提供了一个基本框架,以渗出物管理和耐应力品种的选择为中心。
{"title":"Morphological, Physiological and Metabolomic Responses of Mulberry to Cadmium Exposure: Unveiling Dose-Dependent Tolerance and Activation Mechanism.","authors":"Lian Chen, Changyu Qiu, Gaocong Li, Qiang Lin, Jiehua Chen, Lingyun Sun, Dan Liu, Sen Lin, Dan Wang, Jianan Wu, Zhiyi Li, Yuan Wang, Zhenjiang Wang","doi":"10.1111/pce.70352","DOIUrl":"https://doi.org/10.1111/pce.70352","url":null,"abstract":"<p><p>This study investigated the mechanisms of cadmium (Cd) tolerance and root exudate-mediated soil activation in mulberry (Morus alba L.), a promising species for phytoremediation. Hydroponic experiments with Cd-tolerant seedlings exposed to 5 and 50 mg/L Cd revealed a biphasic concentration-dependent response. Low Cd induced negligible biological effects, whereas high Cd triggered substantial disturbances across multiple biological levels, including morphological alterations, physiological dysregulation and disrupted elemental accumulation patterns. Metabolomic profiling indicated that Cd stress significantly altered the secretion patterns of 17 root exudate metabolites in mulberry, exemplified by the upregulation of sucrose, lactose and 4-acetylbutyric acid, and the downregulation of β-alanine and myo-inositol. Further pathway enrichment analysis linked these differential metabolites to 17 metabolic pathways, with carbohydrate and amino acid metabolism as the main Cd-responsive pathways, suggesting their core role in mediating mulberry's Cd resistance. Root exudates enhanced soil Cd mobilisation in a positive concentration-dependent yet negative time-dependent manner. Consequently, mulberry adapts to Cd stress via metabolic reprogramming of root exudates-a strategic trade-off that serves a dual role by enhancing plant tolerance while simultaneously increasing Cd bioavailability in the soil. This insight provides a foundational framework for phytoremediation, centred on exudate management and the selection of stress-tolerant varieties.</p>","PeriodicalId":222,"journal":{"name":"Plant, Cell & Environment","volume":" ","pages":""},"PeriodicalIF":6.3,"publicationDate":"2025-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145848439","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Liu Li, Hewen Li, Qinghua Liu, Chaoqun Chen, Shulan Wu, Lin Luo, Xueyong Pang, Chunying Yin
The mechanisms of selenium (Se) oxyanion transformation in endophytic bacteria remain poorly understood, which limits their application in biofortification and phytoremediation. Here, we investigated these mechanisms using the plant-growth-promoting (PGP) endophyte Erwinia sp. PSI-03. Under 2 mM selenite stress, the strain intracellularly and extracellularly produced spherical selenium nanoparticles (SeNPs; ab57 nm average diameter). Multi-omics analyses revealed that these SeNPs were formed through parallel enzymatic (mediated by sulfite reductase, cysI) and non-enzymatic (via glutathione and l-cysteine) reduction pathways. Additionally, γ-glutamyl-Se-methylselenocysteine was identified as a key organo-selenium metabolite. Selenite exposure induced extensive reprogramming of the metabolome and transcriptome, highlighting key roles for glutathione metabolism and stress response systems related to cell wall/membrane maintenance, oxidative phosphorylation, two-component signaling systems, and DNA repair. Intriguingly, selenite stress concurrently stimulated bacterial synthesis of PGP compounds, including the auxin precursor indole-3-pyruvate, the defense hormone salicylic acid, and acetate. Consistent with this, under selenite-free and high-selenite (12 mg kg-1 Se) conditions, inoculation with Erwinia sp. PSI-03 significantly promoted tea plant growth. Compared to uninoculated controls, the leaf biomass increased by 52.8% and 51.7%, and the total biomass by 82.9% and 49.6%, respectively. These findings establish a paradigm where endophytic bacteria simultaneously detoxify Se and promote plant health, offering a robust strategy for agricultural and environmental Se management.
{"title":"Erwinia sp. PSI-03 Promotes Plant Growth and Detoxifies Selenite Through Selenium Nanoparticles Biosynthesis.","authors":"Liu Li, Hewen Li, Qinghua Liu, Chaoqun Chen, Shulan Wu, Lin Luo, Xueyong Pang, Chunying Yin","doi":"10.1111/pce.70356","DOIUrl":"https://doi.org/10.1111/pce.70356","url":null,"abstract":"<p><p>The mechanisms of selenium (Se) oxyanion transformation in endophytic bacteria remain poorly understood, which limits their application in biofortification and phytoremediation. Here, we investigated these mechanisms using the plant-growth-promoting (PGP) endophyte Erwinia sp. PSI-03. Under 2 mM selenite stress, the strain intracellularly and extracellularly produced spherical selenium nanoparticles (SeNPs; ab57 nm average diameter). Multi-omics analyses revealed that these SeNPs were formed through parallel enzymatic (mediated by sulfite reductase, cysI) and non-enzymatic (via glutathione and l-cysteine) reduction pathways. Additionally, γ-glutamyl-Se-methylselenocysteine was identified as a key organo-selenium metabolite. Selenite exposure induced extensive reprogramming of the metabolome and transcriptome, highlighting key roles for glutathione metabolism and stress response systems related to cell wall/membrane maintenance, oxidative phosphorylation, two-component signaling systems, and DNA repair. Intriguingly, selenite stress concurrently stimulated bacterial synthesis of PGP compounds, including the auxin precursor indole-3-pyruvate, the defense hormone salicylic acid, and acetate. Consistent with this, under selenite-free and high-selenite (12 mg kg<sup>-1</sup> Se) conditions, inoculation with Erwinia sp. PSI-03 significantly promoted tea plant growth. Compared to uninoculated controls, the leaf biomass increased by 52.8% and 51.7%, and the total biomass by 82.9% and 49.6%, respectively. These findings establish a paradigm where endophytic bacteria simultaneously detoxify Se and promote plant health, offering a robust strategy for agricultural and environmental Se management.</p>","PeriodicalId":222,"journal":{"name":"Plant, Cell & Environment","volume":" ","pages":""},"PeriodicalIF":6.3,"publicationDate":"2025-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145848505","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Heat-Induced Volatiles Enhance Intraspecific Thermotolerance in the Antarctic Pearlwort.","authors":"Rodrigo A Contreras, Gustavo E Zúñiga","doi":"10.1111/pce.70354","DOIUrl":"https://doi.org/10.1111/pce.70354","url":null,"abstract":"","PeriodicalId":222,"journal":{"name":"Plant, Cell & Environment","volume":" ","pages":""},"PeriodicalIF":6.3,"publicationDate":"2025-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145848503","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The direct response of stomata to temperature (DRST, the response with the leaf-to-air vapor gradient, Δw, held constant) is poorly studied due to the difficulty of keeping Δw constant while changing leaf temperature. Most published data suggest a positive response, though the mechanisms behind such a response are unknown. We propose that a hydraulic mechanism should contribute to the DRST, wherein temperature decreases the viscosity of water, increasing hydraulic conductance and thereby increasing leaf water potential, which in turn drives stomatal opening. Because the sensitivity of leaf water potential to changes in hydraulic conductance should be proportional to transpiration rate and hence to Δw, this mechanism predicts a stronger positive DRST at higher Δw than at lower Δw. We tested this prediction by measuring the DRST at two different values of Δw, in six diverse angiosperm species. Our results are consistent with the hypothesis that a hydraulic mechanism contributes to the DRST, though the response varies widely across species, and in three of six species the effect of Δw was far stronger than predicted from theory, suggesting a role for other mechanisms in enhancing the effect of Δw on the DRST.
{"title":"The Stomatal Response to Temperature Is Enhanced by High Evaporative Demand, Consistent With a Partially Hydraulic Mechanism.","authors":"Colleen Mills, Megan K Bartlett, Thomas N Buckley","doi":"10.1111/pce.70347","DOIUrl":"https://doi.org/10.1111/pce.70347","url":null,"abstract":"<p><p>The direct response of stomata to temperature (DRST, the response with the leaf-to-air vapor gradient, Δw, held constant) is poorly studied due to the difficulty of keeping Δw constant while changing leaf temperature. Most published data suggest a positive response, though the mechanisms behind such a response are unknown. We propose that a hydraulic mechanism should contribute to the DRST, wherein temperature decreases the viscosity of water, increasing hydraulic conductance and thereby increasing leaf water potential, which in turn drives stomatal opening. Because the sensitivity of leaf water potential to changes in hydraulic conductance should be proportional to transpiration rate and hence to Δw, this mechanism predicts a stronger positive DRST at higher Δw than at lower Δw. We tested this prediction by measuring the DRST at two different values of Δw, in six diverse angiosperm species. Our results are consistent with the hypothesis that a hydraulic mechanism contributes to the DRST, though the response varies widely across species, and in three of six species the effect of Δw was far stronger than predicted from theory, suggesting a role for other mechanisms in enhancing the effect of Δw on the DRST.</p>","PeriodicalId":222,"journal":{"name":"Plant, Cell & Environment","volume":" ","pages":""},"PeriodicalIF":6.3,"publicationDate":"2025-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145848484","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}