Metabolomic Insights into Cross-Feeding Interactions Between Priestia megaterium PM and Pseudomonas fluorescens NO4: Unveiling Microbial Communication in Plant Growth-Promoting Rhizobacteria.

IF 3.3 3区 生物学 Q2 ECOLOGY
Nompumelelo R Sibanyoni, Lizelle A Piater, Pavel Kerchev, Ntakadzeni E Madala, Msizi I Mhlongo
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引用次数: 0

Abstract

Plant growth-promoting rhizobacteria (PGPR) engage in complex chemical exchange and signalling processes to enhance their survival, rhizosphere colonisation, and plant-beneficial roles. These microbial interactions are mediated by various chemical cues, including quorum sensing (QS) molecules, cyclic peptides, lipopeptides, nutrients, volatile organic compounds (VOC), and phytohormones. Cross-feeding, where one microorganism consumes metabolites produced by another, exemplifies direct chemical communication that shapes community dynamics and metabolic cooperation. However, the effects of cross-feeding among different PGPR strains remain insufficiently characterised. In this study, an LC-MS-based metabolomics approach, combined with multivariate statistical analysis, was employed to investigate metabolic perturbations induced by cross-feeding among PGPR strains. Growth curve analysis revealed that cross-fed PGPR exhibited growth patterns comparable to controls, with a slight reduction in biomass. Metabolic profiling indicated time-dependent shifts in the metabolic state of the cross-fed organisms, suggesting adaptive metabolic reprogramming in response to the donor-conditioned media. Multivariate analysis identified distinct metabolite alterations between cross-fed and control groups across different time points, highlighting the influence of nutrient availability on microbial growth dynamics. Notably, cross-fed groups showed decreased levels of primary metabolites such as amino acids and sugars alongside increased production of secondary metabolites, including surfactins, salicylic acid, and carboxylic acids. These secondary metabolites are implicated in plant growth promotion and defence, indicating their potential as natural biostimulants. The findings advance the understanding of PGPR interactions and chemical communication in the rhizosphere, supporting the development of sustainable agricultural practices by leveraging beneficial microbial interactions. Future research should explore these interactions within more complex microbial communities.

巨孢假单胞菌PM与荧光假单胞菌NO4交叉取食相互作用的代谢组学研究:揭示促进植物生长的根杆菌中的微生物交流。
促进植物生长的根瘤菌(PGPR)参与复杂的化学交换和信号传递过程,以提高其生存、根际定植和植物益处。这些微生物相互作用是由各种化学线索介导的,包括群体感应(QS)分子、环肽、脂肽、营养物质、挥发性有机化合物(VOC)和植物激素。交叉进食,即一种微生物消耗另一种微生物产生的代谢物,是形成群落动态和代谢合作的直接化学交流的例证。然而,在不同的PGPR菌株之间交叉饲养的影响仍然没有充分的表征。本研究采用基于lc - ms的代谢组学方法,结合多元统计分析,研究了PGPR菌株间交叉饲养引起的代谢扰动。生长曲线分析显示,交叉饲养的PGPR表现出与对照相当的生长模式,生物量略有减少。代谢分析表明,交叉喂养的生物体的代谢状态发生了时间依赖性的变化,这表明适应性代谢重编程是对供体条件培养基的反应。多变量分析发现,在不同的时间点上,交叉饲养组和对照组之间的代谢物发生了明显的变化,突出了养分有效性对微生物生长动力学的影响。值得注意的是,交叉喂养组显示出氨基酸和糖等初级代谢物水平下降,而次级代谢物(包括表面素、水杨酸和羧酸)的产量增加。这些次生代谢物与植物生长促进和防御有关,表明它们作为天然生物刺激素的潜力。这些发现促进了对PGPR相互作用和根际化学交流的理解,通过利用有益的微生物相互作用来支持可持续农业实践的发展。未来的研究应该在更复杂的微生物群落中探索这些相互作用。
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来源期刊
Microbial Ecology
Microbial Ecology 生物-海洋与淡水生物学
CiteScore
6.90
自引率
2.80%
发文量
212
审稿时长
3-8 weeks
期刊介绍: The journal Microbial Ecology was founded more than 50 years ago by Dr. Ralph Mitchell, Gordon McKay Professor of Applied Biology at Harvard University in Cambridge, MA. The journal has evolved to become a premier location for the presentation of manuscripts that represent advances in the field of microbial ecology. The journal has become a dedicated international forum for the presentation of high-quality scientific investigations of how microorganisms interact with their environment, with each other and with their hosts. Microbial Ecology offers articles of original research in full paper and note formats, as well as brief reviews and topical position papers.
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