三叶松与柑橘砧木:通过微生物和代谢重编程重塑柠檬根际微生态。

IF 4 2区 生物学 Q2 MICROBIOLOGY
Frontiers in Microbiology Pub Date : 2025-09-24 eCollection Date: 2025-01-01 DOI:10.3389/fmicb.2025.1650631
Chunrui Long, Xiaomeng Fu, Qingjiang Wu, Shaohua Wang, Xianyan Zhou, Jiamei Mao, Lina Guo, Wenbin Shi, Hongxia Yang, Tiankun Yang, Yuxia Du, Jianqiang Yue, Dongming Wu, Hongming Liu
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引用次数: 0

摘要

简介:三叶橙(Poncirus trifoliataL)。“紫阳香城”(Citrus junos Sieb.)。(如Tanaka)是中国柠檬生产的主要砧木,表现出对土壤pH值的不同适应和对植物恢复力的不同影响。砧木作为接穗-土壤相互作用的关键媒介,因其对根际微生物群落和代谢物的调控潜力而成为研究的重点对象。方法:将柠檬(Citrus × limon“Eureka”)幼树嫁接到三叶橙(PTL)和紫阳香城(CJL)砧木上,建立盆栽体系。综合宏基因组学和GC-MS代谢组学方法分析根际微生物群落和代谢物。结果:根际微生物α-多样性(丰富度)差异不显著,但均匀性较高。β-多样性和LEfSe分析显示群落结构差异显著。共鉴定出3门15个差异富集属,其中CJL中的Pseudomonas、Cupriavidus和Burkholderia以及PTL中的Sphingobium表现出较强的富集作用。随机森林模型鉴定出15种关键差异代谢物,其中4种在CJL中显著上调,11种在PTL中显著上调。微生物-代谢物相关性和GSEA分析揭示了涉及遗传信息处理、能量代谢、环境适应和抗病机制的10个核心途径。土壤分析结果表明,CJL的有机质含量、过氧化氢酶活性和株高均显著高于PTL,而PTL的纤维素酶、蔗糖酶和脲酶活性显著高于PTL。在机制上,PTL似乎通过1-单硬脂素分泌来招募地中海假单胞菌,激活甘油脂代谢,增强耐旱性。其咖啡酸和水杨醇-β-葡萄糖苷分泌物可能调动鞘脂和Ensifer粘附素调节氨基糖代谢,促进碳固存和根防御。相反,CJL可能通过l -丙氨酸渗出招募恶臭假单胞菌,通过精氨酸-脯氨酸代谢触发胞外多糖的生物合成,作为关键的耐受机制(如耐旱、耐碱)。讨论:研究结果阐明了根茎对根际微生态系统的特异性调节,突出了不同的微生物-代谢物相互作用和耐受性机制。这些结果为柑橘的精准砧木选择和微生物组工程提供了理论支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Poncirus trifoliata vs. Citrus junos rootstocks: reshaping lemon rhizosphere microecology through microbial and metabolic reprogramming.

Introduction: Trifoliate orange (Poncirus trifoliataL. Raf) and "Ziyang Xiangcheng" (Citrus junos Sieb. ex Tanaka) are the predominant rootstocks for lemon production in China, exhibiting distinct adaptations to soil pH and differential impacts on plant resilience. As pivotal mediators of scion-soil interactions, rootstocks have emerged as key research targets for their regulatory potential in rhizosphere microbial communities and metabolites.

Methods: Pot-cultured systems were established with lemon (Citrus × limon "Eureka") saplings grafted onto trifoliate orange (PTL) and "Ziyang Xiangcheng" (CJL) rootstocks. Integrated metagenomic and GC-MS metabolomic approaches were employed to analyze rhizosphere microbial communities and metabolites.

Results: The results demonstrated no significant difference in rhizospheric microbial α-diversity (richness) between PTL and CJL, although PTL exhibited higher evenness. β-Diversity and LEfSe analysis revealed significant structural divergence in communities. A total of 15 differentially enriched genera across three phyla were identified, among which Pseudomonas, Cupriavidus, and Burkholderia in CJL, along with Sphingobium in PTL, exhibited strong effects. Random forest modeling identified 15 key differential metabolites, with 4 significantly upregulated in CJL and 11 in PTL. Microbial-metabolite correlation and GSEA analysis uncovered 10 core pathways involving genetic information processing, energy metabolism, environmental adaptation, and disease resistance mechanisms. Soil analysis showed CJL significantly surpassed PTL in organic matter content, catalase activity and plant height, whereas PTL exhibited superior cellulase, sucrase and urease activities. Mechanistically, PTL appears to recruit Pseudomonas mediterranea via 1-Monostearin secretion to activate glycerolipid metabolism, enhancing drought tolerance. Its caffeate and salicyl alcohol-β-glucoside secretions potentially mobilize Sphingobium and Ensifer adhaerens to regulate amino sugar metabolism, promoting carbon sequestration and root defense. Conversely, CJL likely employs L-alanine exudation to recruit Pseudomonas putida, triggering exopolysaccharide biosynthesis through arginine-proline metabolism as a key tolerance mechanism (such as drought tolerance and alkali tolerance).

Discussion: The findings elucidate rootstock-specific modulation of rhizosphere microecosystems, highlighting distinct microbial-metabolite interactions and tolerance mechanisms. These results provide theoretical support for precision rootstock selection and microbiome engineering to advance sustainable citrus production.

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来源期刊
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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