Iron limitation-induced endophytic Ammoniphilus assemblage promotes root apoplastic iron remobilization by attenuation of salicylic acid pathways.

IF 9.2 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Lin Zhu, Aijing Zhang, Jiansheng Guo, Huabing Liu, Yue Xie, Xiaomin Lu, Congsheng Yan, Jianfei Wang, Cheng Zhou
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Abstract

Plants establish symbiotic associations with root-colonizing microbes to adapt to adverse conditions. However, how root-associated microbiota interacted with their hosts to improve plant growth under nutrient deficient conditions remains poorly understood. In this study, we explored an interaction between tomato plants and root-associated microbiota under iron (Fe) limitation, mediated by bacterial secretion of glutamine. 16S rRNA gene sequencing revealed that Fe-limited conditions altered the composition of root-associated microbiomes, resulting in the enrichment of Ammoniphilus sp. This taxon was isolated and shown to alleviate Fe deficiency symptoms. Moreover, Fe deficiency triggered salicylic acid (SA)-induced hydrogen peroxide (H2O2) burst, thereby inhibiting the exudation of Fe-mobilizing phenolics from the roots. However, bacterial secretion of Gln greatly attenuated the SA-induced H2O2 production in the roots, thereby enhancing bacterial colonization and promoting apoplastic Fe remobilization. Collectively, these results underscored a microbial strategy for orchestrating plant SA pathways to facilitate the reutilization of root apoplastic Fe.

铁限制诱导的内生嗜氨菌组合通过衰减水杨酸途径促进根外体铁的再动员。
植物与根定殖微生物建立共生关系以适应不利条件。然而,在营养缺乏的条件下,根系相关微生物群如何与宿主相互作用以改善植物生长仍知之甚少。在这项研究中,我们探索了铁(Fe)限制下番茄植株与根相关微生物群之间的相互作用,该相互作用是由细菌分泌谷氨酰胺介导的。16S rRNA基因测序显示,铁限制条件改变了根相关微生物组的组成,导致氨philus sp.的富集。该分类群被分离出来并显示出减轻铁缺乏症状。此外,铁缺乏引发水杨酸(SA)诱导的过氧化氢(H2O2)爆发,从而抑制了铁动员酚类物质从根部渗出。然而,细菌分泌Gln大大减弱了sa诱导的根中H2O2的产生,从而增强了细菌的定植,促进了铁的再活化。总的来说,这些结果强调了微生物策略,以协调植物SA途径,促进根外体铁的再利用。
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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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