{"title":"Low-nitrogen input enriches Massilia bacteria in the phyllosphere to improve blast resistance in rice.","authors":"Qiong Huang,Rongfeng Wang,Qihui Ding,Fang Liao,Linxing Zhu,Mengting Huang,Jia Li,Jixing Zeng,Qirong Shen,Min Wang,Shiwei Guo","doi":"10.1111/nph.70582","DOIUrl":null,"url":null,"abstract":"Excessive nitrogen (N) fertilization exacerbates rice blast disease caused by Magnaporthe oryzae, yet the underlying microbiological mechanisms remain unclear. Through integrated field surveys and controlled experiments, we demonstrate that high-N application worsens disease severity by disrupting microbiome communities in the phyllosphere of rice (Oryza sativa) plants. We identified microorganisms in the phyllosphere through 16S rDNA sequencing. Low-N conditions were associated with a greater Massilia bacterial population, which was negatively correlated with pathogen abundance and disease index. In vitro and in vivo experiments indicated that Massilia enhances rice resistance to rice blast disease. We explored how Massilia confers resistance. Massilia strain z571 directly inhibited M. oryzae spore germination and hyphal invasion while also activating host immunity, including elevated levels of salicylic acid and jasmonic acid, enhanced expression of defense-related genes, and increased activity of antioxidant defense enzymes. Moreover, Massilia exhibited broad-spectrum antagonism against multiple pathogens. Our findings unveil a microbiome-mediated mechanism linking N fertilization to disease susceptibility and highlight Massilia as a potential biocontrol agent, offering a sustainable strategy for managing rice blast through optimized fertilization practices and microbial interventions.","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"1 1","pages":""},"PeriodicalIF":8.1000,"publicationDate":"2025-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Phytologist","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/nph.70582","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
Excessive nitrogen (N) fertilization exacerbates rice blast disease caused by Magnaporthe oryzae, yet the underlying microbiological mechanisms remain unclear. Through integrated field surveys and controlled experiments, we demonstrate that high-N application worsens disease severity by disrupting microbiome communities in the phyllosphere of rice (Oryza sativa) plants. We identified microorganisms in the phyllosphere through 16S rDNA sequencing. Low-N conditions were associated with a greater Massilia bacterial population, which was negatively correlated with pathogen abundance and disease index. In vitro and in vivo experiments indicated that Massilia enhances rice resistance to rice blast disease. We explored how Massilia confers resistance. Massilia strain z571 directly inhibited M. oryzae spore germination and hyphal invasion while also activating host immunity, including elevated levels of salicylic acid and jasmonic acid, enhanced expression of defense-related genes, and increased activity of antioxidant defense enzymes. Moreover, Massilia exhibited broad-spectrum antagonism against multiple pathogens. Our findings unveil a microbiome-mediated mechanism linking N fertilization to disease susceptibility and highlight Massilia as a potential biocontrol agent, offering a sustainable strategy for managing rice blast through optimized fertilization practices and microbial interventions.
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.