• ISSN 1008-505X
  • CN 11-3996/S

盐胁迫下接种DSE对苦豆子根系分泌物的调控作用

The regulatory effect of inoculation with dark septate endophyte on root exudates of Sophora alopecuroides L. under salt stress

  • 摘要:
    目的 耐盐植物苦豆子(Sophora alopecuroides)在盐碱地修复中具有重要价值。本研究旨在揭示深色有隔内生真菌(dark septate endophytes,DSE)调控苦豆子生长、增强其耐盐性的代谢途径,为植物-微生物互作调控盐碱逆境提供理论支撑。
    方法 以苦豆子为试验材料进行了水培试验。营养液设置5个Na2SO4盐浓度(0%、0.15%、0.3%、0.45%、1%)下接种和未接种DSE处理,共30个样本(5×2×3重复)。苦豆子在营养液中生长至90天后,收获并收集根系分泌物,测定植株生物量、离子含量以及根系形态,利用超高效液相色谱-四极杆飞行时间质谱技术(UPLC-QTOF-MS)进行根系分泌物的非靶向代谢组学分析。比较不同盐浓度和接菌双因素对苦豆子生长的影响,阐明DSE对苦豆子生物量积累、离子稳态、代谢产物的调控作用,最终,通过路径分析获得各变量之间的响应关系,揭示DSE促进苦豆子耐盐机理。
    结果 Na2SO4胁迫导致苦豆子生物量减少,干重降低了10.8%~65.2%。接种DSE对苦豆子有显著的生物刺激作用,相较于同盐浓度下未接种处理,苦豆子生物量增加了93%~254%,根长增加了4%~181%,DSE促生效应在0.3% Na2SO4胁迫下最为显著;接菌苦豆子K+含量增加了53%~108%,Na+/K+的比值降低了23%~33%。代谢组学显示DSE特异性诱导甘油磷脂代谢和类胡萝卜素生物合成等4条核心通路,促进了脂质、类胡萝卜素等代谢物的合成,通过磷脂重塑增强膜稳定性和类胡萝卜素清除ROS等形成了耐盐防御机制。相关性分析表明,接菌与植物生物量、根系形态、离子含量和代谢物含量有显著相关关系,路径分析表明接菌与糖基磷脂酰肌醇生物合成、甘油脂代谢和类胡萝卜素生物合成显著正相关,与果糖和甘露糖代谢显著负相关,4条核心代谢通路共同作用于苦豆子根系生长,影响植物Na+/K+平衡。
    结论 DSE通过上调脂质和类胡萝卜素等代谢物,激活膜稳定性与ROS清除通路,并通过促进K+吸收,维持Na+/K+平衡,有效促进苦豆子生长和根系发育,增强其抗盐能力。

     

    Abstract:
    Objectives The salt-tolerant plant Sophora alopecuroides L.holds immense potential in the restoration of saline-alkali soil. This study delved the regulatory effects of dark septate endophytes (DSE) inoculation on growth performance and metabolic responses in S. alopecuroides under salt stress conditions, offering theoretical backing for the ecological restoration of plant-microbial interaction in saline-alkali land.
    Methods A controlled hydroponic system was implemented at Xi’an University of Science and Technology using S alopecuroides as the test material. Five distinct concentrations of Na2SO4 salts (0%, 0.15%, 0.3%, 0.45%, 1%) and two groups of treatments (inoculated with DSE and uninoculated control, CK) were set up, with a total of 30 samples (5×2×3 replicates). After the plants have grown in the nutrient solution for 90 days, the root exudates of the plants were collected. and the plant biomass accumulation, ion content (Na+, K+, Ca2+, Mg2+), and root morphology parameters (total length, surface area, tip number) were quantitatively assessed. In the detection of root exudates, ultra-high performance liquid chromatogre-quadrupole time-of-flight mass spectrometry (UPLC-QTOF-MS) was used for non-targeted metabolomics analysis. Comparative analysis was conducted to evaluate the two-factor effects (salt concentration and inoculation) on plant growth, aiming to elucidate DSE-mediated regulation of biomass accumulation, ion homeostasis, and metabolite profiles in S. alopecuroides, and employ pathway analysis to establish response relationships among variables, ultimately revealing the mechanisms underlying DSE-enhanced salt tolerance.
    Results Na2SO4 stress significantly reduced S. alopecuroides biomass. The dry weight of S. alopecuroides decreased by 10.8%−65.2%. Inoculation with DSE had a significant biological stimulating effect on S. alopecuroides. Compared with the control (CK) at the identical salt concentration, biomass of the S. alopecuroides increased by 93%−254%, root length by 4%−181%. The promotional effects of DSE were the most pronounced under 0.3% Na2SO4 stress. The K+ content of inoculated S. alopecuroides increased by 53%-108%, the ratio of Na+/K+ decreased by 23%-33%. Metabolic analysis uncovered that DSE specifically triggered four core pathways such as glycerol phospholipid metabolism and carotenoid biosynthesis, and boosted the synthesis of metabolites such as lipids and carotenoids. It forms a salt-tolerant defense mechanism by enhancing membrane stability through phospholipid remodeling and carotenoid scavenging of ROS. Correlation analysis demonstrated that inoculation was significantly correlated with plant biomass, root morphology, ion content and metabolite content. Path analysis revealed that inoculation exhibited significant positive correlations with glycosylphosphatidylinositol (GPI) biosynthesis, glycerolipid metabolism, and carotenoid biosynthesis, while demonstrating significant negative correlations with fructose and mannose metabolism in S. alopecuroides. These four core metabolic pathways collectively regulated root growth and modulating Na+/K+ balance.
    Conclusion DSE activates pathways for membrane stabilization and ROS scavenging by upregulating metabolites such as lipids and carotenoids. It also facilitates K+ uptake and maintaines Na+/K+ balance, thereby effectively promoting the growth and root development of S. alopecuroides and enhancing their salt resistance.

     

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