T Bose, T G Mahomed, K C Mbatha, J C Joubert, A Hammerbacher
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Metabolite profiling indicated that shoot tips had a higher relative abundance of primary and secondary metabolites, including sugars, fatty acids, organic acids, phenolic acid derivatives and salicinoids, while wood was enriched in flavonoids. Bacterial biodiversity also differed significantly between these tissues, with Clostridiales, Bacteroidales and Bacillales dominating in shoot tips, associated with rapid growth and anaerobic fermentation, while wood tissues were characterized by diazotrophs from Rhizobiales, Sphingomonadales and Frankiales. PCoA clustering confirmed tissue-specific microbial differences. Functional analysis revealed an enrichment of fundamental cellular processes in shoot tips, while wood exhibited pathways related to degradation and mortality. Metabolite profiling revealed significant variations in primary and secondary metabolites, highlighting their influence on microbial biodiversity across plant tissues. The dominance of specific bacterial orders and distinct functional pathways in each tissue suggests a tailored microbial response to the unique environments of shoot tips and wood.</p>","PeriodicalId":220,"journal":{"name":"Plant Biology","volume":" ","pages":""},"PeriodicalIF":4.2000,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Tissue ontogeny and chemical composition influence bacterial biodiversity in the wood and shoot tip of Populus nigra.\",\"authors\":\"T Bose, T G Mahomed, K C Mbatha, J C Joubert, A Hammerbacher\",\"doi\":\"10.1111/plb.13724\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Plant-microbe interactions significantly influence plant growth dynamics and adaptability. This study explores the impact of metabolites on microbial biodiversity in shoot tips and wood of Populus nigra under greenhouse conditions, using high-throughput sequencing and metabolite profiling. Branches from P. nigra were harvested, rooted, and transplanted into pots for growth. After 3 months, tissue samples from shoot tips and wood were collected, and metabolites extracted and analysed using GC-MS and LC-MS. Genomic DNA was extracted and subjected to high-throughput sequencing for bacterial biodiversity profiling. Both datasets were analysed using bioinformatic and statistical pipelines. Metabolite profiling indicated that shoot tips had a higher relative abundance of primary and secondary metabolites, including sugars, fatty acids, organic acids, phenolic acid derivatives and salicinoids, while wood was enriched in flavonoids. Bacterial biodiversity also differed significantly between these tissues, with Clostridiales, Bacteroidales and Bacillales dominating in shoot tips, associated with rapid growth and anaerobic fermentation, while wood tissues were characterized by diazotrophs from Rhizobiales, Sphingomonadales and Frankiales. PCoA clustering confirmed tissue-specific microbial differences. Functional analysis revealed an enrichment of fundamental cellular processes in shoot tips, while wood exhibited pathways related to degradation and mortality. Metabolite profiling revealed significant variations in primary and secondary metabolites, highlighting their influence on microbial biodiversity across plant tissues. 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引用次数: 0
摘要
植物与微生物之间的相互作用对植物的生长动态和适应性有重大影响。本研究利用高通量测序和代谢物分析方法,探讨了在温室条件下代谢物对黑杨嫩枝尖和木材中微生物生物多样性的影响。黑杨的枝条被采收、生根并移植到花盆中生长。3 个月后,收集枝梢和木质部的组织样本,提取代谢物并使用 GC-MS 和 LC-MS 进行分析。提取基因组 DNA 并进行高通量测序,以分析细菌的生物多样性。利用生物信息学和统计学方法对这两个数据集进行了分析。代谢物分析表明,嫩枝尖端的初级和次级代谢物相对含量较高,包括糖类、脂肪酸、有机酸、酚酸衍生物和水杨酸类,而木质部则富含黄酮类化合物。这些组织的细菌生物多样性也有显著差异,芽尖主要是梭状芽孢杆菌属、类杆菌属和芽孢杆菌属,与快速生长和厌氧发酵有关,而木质部组织的特点是根瘤菌属、鞘氨醇单胞菌属和弗兰科菌属的重氮营养体。PCoA 聚类证实了特定组织的微生物差异。功能分析显示,芽尖富含基本的细胞过程,而木材则表现出与降解和死亡有关的途径。代谢物分析表明,初级和次级代谢物存在显著差异,凸显了它们对植物组织中微生物生物多样性的影响。每个组织中特定细菌群和不同功能途径的优势表明,微生物对嫩梢和木材的独特环境做出了量身定制的反应。
Tissue ontogeny and chemical composition influence bacterial biodiversity in the wood and shoot tip of Populus nigra.
Plant-microbe interactions significantly influence plant growth dynamics and adaptability. This study explores the impact of metabolites on microbial biodiversity in shoot tips and wood of Populus nigra under greenhouse conditions, using high-throughput sequencing and metabolite profiling. Branches from P. nigra were harvested, rooted, and transplanted into pots for growth. After 3 months, tissue samples from shoot tips and wood were collected, and metabolites extracted and analysed using GC-MS and LC-MS. Genomic DNA was extracted and subjected to high-throughput sequencing for bacterial biodiversity profiling. Both datasets were analysed using bioinformatic and statistical pipelines. Metabolite profiling indicated that shoot tips had a higher relative abundance of primary and secondary metabolites, including sugars, fatty acids, organic acids, phenolic acid derivatives and salicinoids, while wood was enriched in flavonoids. Bacterial biodiversity also differed significantly between these tissues, with Clostridiales, Bacteroidales and Bacillales dominating in shoot tips, associated with rapid growth and anaerobic fermentation, while wood tissues were characterized by diazotrophs from Rhizobiales, Sphingomonadales and Frankiales. PCoA clustering confirmed tissue-specific microbial differences. Functional analysis revealed an enrichment of fundamental cellular processes in shoot tips, while wood exhibited pathways related to degradation and mortality. Metabolite profiling revealed significant variations in primary and secondary metabolites, highlighting their influence on microbial biodiversity across plant tissues. The dominance of specific bacterial orders and distinct functional pathways in each tissue suggests a tailored microbial response to the unique environments of shoot tips and wood.
期刊介绍:
Plant Biology is an international journal of broad scope bringing together the different subdisciplines, such as physiology, molecular biology, cell biology, development, genetics, systematics, ecology, evolution, ecophysiology, plant-microbe interactions, and mycology.
Plant Biology publishes original problem-oriented full-length research papers, short research papers, and review articles. Discussion of hot topics and provocative opinion articles are published under the heading Acute Views. From a multidisciplinary perspective, Plant Biology will provide a platform for publication, information and debate, encompassing all areas which fall within the scope of plant science.