{"title":"Dual-functionality of Nocardiopsis alba B57 in biocontrol and plant growth: a metabolomic approach to agricultural sustainability.","authors":"Osama Abdalla Abdelshafy Mohamad, Yong-Hong Liu, Tamer Elsamahy, Shuai Li, Rajivgandhi Govindan, Nigora Kuchkarova, Shaimaa Hatab, Yuanming Zhang, Wen-Jun Li","doi":"10.1038/s41522-025-00796-6","DOIUrl":null,"url":null,"abstract":"<p><p>The increasing incidence of fungal phytopathogens poses a significant challenge to agricultural sustainability, necessitating the development of environmental alternatives to synthetic fungicides and mitigating their ecological impact. This study explores the efficiency of Nocardiopsis alba B57 to produce secondary metabolites with antifungal and plant growth-promoting properties. Untargeted metabolomics using ultra-high-performance liquid chromatography (UPLC-MS/MS) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses identified key metabolites (e.g., carbapenem, menaquinone, and fumiquinazoline) in the co-culture environment with fungal pathogens. Additionally, principal component analysis and OPLS-DA differentiated monoculture and co-culture metabolic profiles, revealed carbapenem biosynthesis as a highly enriched pathway. The comprehensive metabolomics data and the statistical analysis of the identified metabolites confirmed that co-culturing of B57 and fungal strains showed upregulated metabolites (e.g., carbapenem and menaquinone). However, other metabolites (e.g., mupirocin) were downregulated and significantly suppressed. These changes in metabolic activity reflect the organism's adaptive and competitive responses during the co-culture conditions with fungal pathogens and influence plant hormone signaling (e.g., auxin and cytokinin), promoting plant growth and disease resistance. These findings underscore B57's adaptive biosynthetic response to co-culture conditions, supporting its use as a sustainable biocontrol agent and boosting crop productivity.</p>","PeriodicalId":19370,"journal":{"name":"npj Biofilms and Microbiomes","volume":"11 1","pages":"164"},"PeriodicalIF":9.2000,"publicationDate":"2025-08-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12361581/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"npj Biofilms and Microbiomes","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1038/s41522-025-00796-6","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The increasing incidence of fungal phytopathogens poses a significant challenge to agricultural sustainability, necessitating the development of environmental alternatives to synthetic fungicides and mitigating their ecological impact. This study explores the efficiency of Nocardiopsis alba B57 to produce secondary metabolites with antifungal and plant growth-promoting properties. Untargeted metabolomics using ultra-high-performance liquid chromatography (UPLC-MS/MS) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses identified key metabolites (e.g., carbapenem, menaquinone, and fumiquinazoline) in the co-culture environment with fungal pathogens. Additionally, principal component analysis and OPLS-DA differentiated monoculture and co-culture metabolic profiles, revealed carbapenem biosynthesis as a highly enriched pathway. The comprehensive metabolomics data and the statistical analysis of the identified metabolites confirmed that co-culturing of B57 and fungal strains showed upregulated metabolites (e.g., carbapenem and menaquinone). However, other metabolites (e.g., mupirocin) were downregulated and significantly suppressed. These changes in metabolic activity reflect the organism's adaptive and competitive responses during the co-culture conditions with fungal pathogens and influence plant hormone signaling (e.g., auxin and cytokinin), promoting plant growth and disease resistance. These findings underscore B57's adaptive biosynthetic response to co-culture conditions, supporting its use as a sustainable biocontrol agent and boosting crop productivity.
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.