Ancient bayberry increased stress resistance by enriching tissue‐specific microbiome and metabolites

IF 3.6 2区 生物学 Q1 PLANT SCIENCES
Gang Li, Zhenshuo Wang, Haiying Ren, Xingjiang Qi, Hao Han, Xiangyang Ding, Li Sun, Rahila Hafeez, Qi Wang, Bin Li
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Abstract

The ancient bayberry demonstrates superior resistance to both biotic and abiotic stresses compared to cultivated bayberry, yet the underlying mechanisms remain largely unexplored. This study investigates whether long‐term bayberry cultivation enhances stress resistance through modulation of tissue‐specific microbes and metabolites. Employing microbiome amplicon sequencing alongside untargeted mass spectrometry analysis, we scrutinize the role of endosphere and rhizosphere microbial communities and metabolites in shaping the differential resistance observed between ancient and cultivated bayberry trees. Our findings highlight the presence of core microbiome and metabolites across various bayberry tissues, suggesting that the heightened resistance of ancient bayberry may stem from alterations in rhizosphere and endosphere microbial communities and secondary metabolites. Specifically, enrichment of Bacillus in roots and stems, Pseudomonas in leaves, and Mortierella in rhizosphere soil of ancient bayberry was noted. Furthermore, correlation analysis underscores the significance of enriched microbial species in enhancing ancient bayberry's resistance to stresses, with elevated levels of resistance‐associated metabolites such as beta‐myrcene, benzothiazole, L‐glutamic acid, and gamma‐aminobutyric acid identified through GC–MS metabolomics analysis. The beneficial role of these resistance‐associated metabolites was further elucidated through assessment of their promotive and allelopathic effects, as well as their phytostatic and antioxidant functions in lettuce plants. Ultimately, our study delves into the intrinsic reasons behind the greater resistance of ancient bayberry to biotic and abiotic stresses by evaluating the impact of long‐term planting on the microbial community and metabolites in the bayberry endosphere and rhizosphere, shedding light on the complex dynamics of host‐microbial interactions.
古老的杨梅通过丰富组织特异性微生物组和代谢物增强了抗压能力
与栽培的杨梅相比,古老的杨梅对生物和非生物胁迫都表现出卓越的抗性,但其潜在机制在很大程度上仍未得到探索。本研究探讨了长期栽培杨梅是否会通过调节组织特异性微生物和代谢物来增强抗逆性。通过微生物组扩增片段测序和非靶向质谱分析,我们仔细研究了内圈和根圈微生物群落和代谢物在形成古老杨梅树和栽培杨梅树之间不同抗性中的作用。我们的研究结果突显了不同杨梅组织中核心微生物群落和代谢物的存在,表明古老杨梅抗性的增强可能源于根圈和内圈微生物群落及次级代谢物的改变。具体而言,研究人员注意到根部和茎部富含芽孢杆菌,叶片富含假单胞菌,根瘤土壤富含莫氏菌。此外,相关性分析强调了富集的微生物物种在增强古杨梅抗逆性方面的重要作用,通过 GC-MS 代谢组学分析发现,β-月桂烯、苯并噻唑、L-谷氨酸和γ-氨基丁酸等抗逆性相关代谢物水平升高。通过评估这些抗性相关代谢物在莴苣植物中的促进作用、等位效应以及植物抑制和抗氧化功能,进一步阐明了它们的有益作用。最终,我们的研究通过评估长期种植对杨梅内圈和根圈微生物群落和代谢物的影响,深入探讨了古老杨梅对生物和非生物胁迫具有更强抵抗力的内在原因,揭示了宿主与微生物相互作用的复杂动态。
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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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