RIN enhances plant disease resistance via root exudate-mediated assembly of disease-suppressive rhizosphere microbiota

根际 生物 放线菌门 微生物群 渗出液 青枯菌 植物抗病性 微生物学 植物 病菌 细菌 遗传学 基因 16S核糖体RNA
作者
Keming Yang,Ruixin Fu,Haichao Feng,Gaofei Jiang,Omri M. Finkel,Tianyu Sun,Mingchun Liu,Baowen Huang,Shan Li,Xiaofang Wang,Tianjie Yang,Yikui Wang,Shimei Wang,Yangchun Xu,Qirong Shen,Ville‐Petri Friman,Alexandre Jousset,Zhong Wei
出处
期刊:Molecular Plant [Elsevier BV]
卷期号:16 (9): 1379-1395 被引量:33
标识
DOI:10.1016/j.molp.2023.08.004
摘要

The RIPENING-INHIBITOR (RIN) transcriptional factor is a key regulator governing fruit ripening. While RIN also affects other physiological processes, its potential roles in triggering interactions with the rhizosphere microbiome and plant health are unknown. Here we show that RIN affects microbiome-mediated disease resistance via root exudation, leading to recruitment of microbiota that suppress the soil-borne, phytopathogenic Ralstonia solanacearum bacterium. Compared with the wild-type (WT) plant, RIN mutants had different root exudate profiles, which were associated with distinct changes in microbiome composition and diversity. Specifically, the relative abundances of antibiosis-associated genes and pathogen-suppressing Actinobacteria (Streptomyces) were clearly lower in the rhizosphere of rin mutants. The composition, diversity, and suppressiveness of rin plant microbiomes could be restored by the application of 3-hydroxyflavone and riboflavin, which were exuded in much lower concentrations by the rin mutant. Interestingly, RIN-mediated effects on root exudates, Actinobacteria, and disease suppression were evident from the seedling stage, indicating that RIN plays a dual role in the early assembly of disease-suppressive microbiota and late fruit development. Collectively, our work suggests that, while plant disease resistance is a complex trait driven by interactions between the plant, rhizosphere microbiome, and the pathogen, it can be indirectly manipulated using "prebiotic" compounds that promote the recruitment of disease-suppressive microbiota.
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