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Pseudomonas fluorescensInduces Strain-Dependent and Strain-Independent Host Plant Responses in Defense Networks, Primary Metabolism, Photosynthesis, and Fitness

生物 荧光假单胞菌 次生代谢 新陈代谢 拟南芥 生物化学 基因 细菌 遗传学 突变体 生物合成
作者
David J. Weston,Dale A. Pelletier,Jennifer L. Morrell‐Falvey,Timothy J. Tschaplinski,Sara Jawdy,Tse-Yuan S. Lu,Sara M. Allen,Sarah J. Melton,Madhavi Z. Martin,Christopher W. Schadt,Abhijit Karve,Jin‐Gui Chen,Xiaohan Yang,Mitchel J. Doktycz,Gerald A. Tuskan
出处
期刊:Molecular Plant-microbe Interactions [American Phytopathological Society]
卷期号:25 (6): 765-778 被引量:95
标识
DOI:10.1094/mpmi-09-11-0253
摘要

Colonization of plants by nonpathogenic Pseudomonas fluorescens strains can confer enhanced defense capacity against a broad spectrum of pathogens. Few studies, however, have linked defense pathway regulation to primary metabolism and physiology. In this study, physiological data, metabolites, and transcript profiles are integrated to elucidate how molecular networks initiated at the root–microbe interface influence shoot metabolism and whole-plant performance. Experiments with Arabidopsis thaliana were performed using the newly identified P. fluorescens GM30 or P. fluorescens Pf-5 strains. Co-expression networks indicated that Pf-5 and GM30 induced a subnetwork specific to roots enriched for genes participating in RNA regulation, protein degradation, and hormonal metabolism. In contrast, only GM30 induced a subnetwork enriched for calcium signaling, sugar and nutrient signaling, and auxin metabolism, suggesting strain dependence in network architecture. In addition, one subnetwork present in shoots was enriched for genes in secondary metabolism, photosynthetic light reactions, and hormone metabolism. Metabolite analysis indicated that this network initiated changes in carbohydrate and amino acid metabolism. Consistent with this, we observed strain-specific responses in tryptophan and phenylalanine abundance. Both strains reduced host plant carbon gain and fitness, yet provided a clear fitness benefit when plants were challenged with the pathogen P. syringae DC3000.
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