Wei Qiu, Jie Kang, Zeming Ye, Shengdie Yang, Xiujun Tu, Penghao Xie, Jingping Ge, Wenxiang Ping, Jun Yuan
{"title":"Arbuscular mycorrhizal fungi build a bridge for soybeans to recruit Pseudomonas putida","authors":"Wei Qiu, Jie Kang, Zeming Ye, Shengdie Yang, Xiujun Tu, Penghao Xie, Jingping Ge, Wenxiang Ping, Jun Yuan","doi":"10.1111/nph.70064","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>\n </p><ul>\n \n <li>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.</li>\n \n <li>To address the above questions, we used soybean (<i>Glycine max</i>), <i>Funneliformis mosseae</i>, and <i>Pseudomonas putida</i> KT2440 as research subjects to establish rhizobiont interactions and to elucidate the signal exchange and division of labor among these components.</li>\n \n <li><i>Funneliformis mosseae</i> can attract <i>P. putida</i> KT2440 by secreting cysteine as a signaling molecule and can promote the colonization of <i>P. putida</i> KT2440 in the soybean rhizosphere. Colonized <i>P. putida</i> KT2440 can stimulate the <span>l</span>-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 <span>l</span>-tryptophan stimulation.</li>\n \n <li>Collectively, we decipher the tripartite mechanism of rhizosphere microbial community assembly via cross-kingdom interactions.</li>\n </ul>\n </div>","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"246 3","pages":"1276-1292"},"PeriodicalIF":8.3000,"publicationDate":"2025-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Phytologist","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/nph.70064","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
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.
期刊介绍:
New Phytologist is an international electronic journal published 24 times a year. It is owned by the New Phytologist Foundation, a non-profit-making charitable organization dedicated to promoting plant science. The journal publishes excellent, novel, rigorous, and timely research and scholarship in plant science and its applications. The articles cover topics in five sections: Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology. These sections encompass intracellular processes, global environmental change, and encourage cross-disciplinary approaches. The journal recognizes the use of techniques from molecular and cell biology, functional genomics, modeling, and system-based approaches in plant science. Abstracting and Indexing Information for New Phytologist includes Academic Search, AgBiotech News & Information, Agroforestry Abstracts, Biochemistry & Biophysics Citation Index, Botanical Pesticides, CAB Abstracts®, Environment Index, Global Health, and Plant Breeding Abstracts, and others.