Arbuscular mycorrhizal fungi build a bridge for soybeans to recruit <i>Pseudomonas putida</i>

The assembly of the rhizosphere microbiome determines its functionality for plant fitness. Although the interactions between arbuscular mycorrhizal fungi (AMF) and plant growth-promoting rhizobacteria (PGPR) play important roles in plant growth and disease resistance, research on the division of labor among the members of the symbionts formed among plants, AMF, and PGPR, as well as the flow of carbon sources, is still insufficient. To address the above questions, we used soybean (Glycine max), Funneliformis mosseae, and Pseudomonas putida KT2440 as research subjects to establish rhizobiont interactions and to elucidate the signal exchange and division of labor among these components. Funneliformis mosseae can attract P. putida KT2440 by secreting cysteine as a signaling molecule and can promote the colonization of P. putida KT2440 in the soybean rhizosphere. Colonized P. putida KT2440 can stimulate the l-tryptophan secretion of the host plant and can lead to the upregulation of genes involved in converting methyl-indole-3-acetic acid (Me-IAA) into IAA in response to l-tryptophan stimulation. Collectively, we decipher the tripartite mechanism of rhizosphere microbial community assembly via cross-kingdom interactions.

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Publication Details

Journal
New Phytologist
Published
2025-03-19
DOI
https://doi.org/10.1111/nph.70064
Citations
20
Primary Topic
Mycorrhizal Fungi and Plant Interactions
Type
article
Field-Weighted Citation Impact
35.00

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article

Arbuscular mycorrhizal fungi build a bridge for soybeans to recruit Pseudomonas putida

Jie Kang, Zeming Ye, Shengdie Yang, Jingping Ge et al.
20 citations
New Phytologist
Mycorrhizal Fungi and Plant Interactions
35.00
article

Arbuscular mycorrhizal fungi build a bridge for soybeans to recruit Pseudomonas putida

Jie Kang, Zeming Ye, Shengdie Yang, Jingping Ge, Wei Qiu, Penghao Xie, Jun Jie Yuan, Wenxiang Ping, Xiujun Tu
article en
20 citations

Abstract

The assembly of the rhizosphere microbiome determines its functionality for plant fitness. Although the interactions between arbuscular mycorrhizal fungi (AMF) and plant growth-promoting rhizobacteria (PGPR) play important roles in plant growth and disease resistance, research on the division of labor among the members of the symbionts formed among plants, AMF, and PGPR, as well as the flow of carbon sources, is still insufficient. To address the above questions, we used soybean (Glycine max), Funneliformis mosseae, and Pseudomonas putida KT2440 as research subjects to establish rhizobiont interactions and to elucidate the signal exchange and division of labor among these components. Funneliformis mosseae can attract P. putida KT2440 by secreting cysteine as a signaling molecule and can promote the colonization of P. putida KT2440 in the soybean rhizosphere. Colonized P. putida KT2440 can stimulate the l-tryptophan secretion of the host plant and can lead to the upregulation of genes involved in converting methyl-indole-3-acetic acid (Me-IAA) into IAA in response to l-tryptophan stimulation. Collectively, we decipher the tripartite mechanism of rhizosphere microbial community assembly via cross-kingdom interactions.

New PhytologistVol. 246(3)
Nanjing Agricultural University (CN), Heilongjiang University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 0%
Mycorrhizal Fungi and Plant Interactions
35.00
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