{"title":"(p)ppGpp施加分级转录变化,损害生物膜的运动性并促进抗生素耐受性。","authors":"Florian Engelhardt, Kathryn Turnbull, Melisa Gür, Mathias Müsken, Matthias Preusse, Susanne Häussler, Mohammad Roghanian","doi":"10.1038/s41522-025-00795-7","DOIUrl":null,"url":null,"abstract":"<p><p>(p)ppGpp is the master regulator of bacterial stress responses, orchestrating cellular physiology via the stringent response to promote survival and adaptation. In response to nutritional challenges and stress, (p)ppGpp extensively rewires the transcriptome. Here, we demonstrate that (p)ppGpp production in Pseudomonas aeruginosa is gradual and relative to stress severity, rather than binary (on/off). Transcriptomic analysis reveals that (p)ppGpp ensures proportionate cellular responses to stress by imposing a layer-by-layer regulation of gene expression. These effects intensify as (p)ppGpp levels rise, with up to a quarter of the genome differentially regulated at maximal levels. Initial increases in (p)ppGpp reduce growth and metabolism while suppressing motility and pyocyanin production. At higher levels, biofilm-related genes are upregulated at the expense of virulence genes, promoting the formation of condensed biofilms. Finally, (p)ppGpp-driven reprogramming induces antimicrobial tolerance, particularly under biofilm conditions, independently of its effects on growth.</p>","PeriodicalId":19370,"journal":{"name":"npj Biofilms and Microbiomes","volume":"11 1","pages":"148"},"PeriodicalIF":9.2000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12316884/pdf/","citationCount":"0","resultStr":"{\"title\":\"(p)ppGpp imposes graded transcriptional changes to impair motility and promote antibiotic tolerance in biofilms.\",\"authors\":\"Florian Engelhardt, Kathryn Turnbull, Melisa Gür, Mathias Müsken, Matthias Preusse, Susanne Häussler, Mohammad Roghanian\",\"doi\":\"10.1038/s41522-025-00795-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>(p)ppGpp is the master regulator of bacterial stress responses, orchestrating cellular physiology via the stringent response to promote survival and adaptation. In response to nutritional challenges and stress, (p)ppGpp extensively rewires the transcriptome. Here, we demonstrate that (p)ppGpp production in Pseudomonas aeruginosa is gradual and relative to stress severity, rather than binary (on/off). Transcriptomic analysis reveals that (p)ppGpp ensures proportionate cellular responses to stress by imposing a layer-by-layer regulation of gene expression. These effects intensify as (p)ppGpp levels rise, with up to a quarter of the genome differentially regulated at maximal levels. Initial increases in (p)ppGpp reduce growth and metabolism while suppressing motility and pyocyanin production. At higher levels, biofilm-related genes are upregulated at the expense of virulence genes, promoting the formation of condensed biofilms. Finally, (p)ppGpp-driven reprogramming induces antimicrobial tolerance, particularly under biofilm conditions, independently of its effects on growth.</p>\",\"PeriodicalId\":19370,\"journal\":{\"name\":\"npj Biofilms and Microbiomes\",\"volume\":\"11 1\",\"pages\":\"148\"},\"PeriodicalIF\":9.2000,\"publicationDate\":\"2025-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12316884/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"npj Biofilms and Microbiomes\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1038/s41522-025-00795-7\",\"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}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"npj Biofilms and Microbiomes","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1038/s41522-025-00795-7","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}
(p)ppGpp imposes graded transcriptional changes to impair motility and promote antibiotic tolerance in biofilms.
(p)ppGpp is the master regulator of bacterial stress responses, orchestrating cellular physiology via the stringent response to promote survival and adaptation. In response to nutritional challenges and stress, (p)ppGpp extensively rewires the transcriptome. Here, we demonstrate that (p)ppGpp production in Pseudomonas aeruginosa is gradual and relative to stress severity, rather than binary (on/off). Transcriptomic analysis reveals that (p)ppGpp ensures proportionate cellular responses to stress by imposing a layer-by-layer regulation of gene expression. These effects intensify as (p)ppGpp levels rise, with up to a quarter of the genome differentially regulated at maximal levels. Initial increases in (p)ppGpp reduce growth and metabolism while suppressing motility and pyocyanin production. At higher levels, biofilm-related genes are upregulated at the expense of virulence genes, promoting the formation of condensed biofilms. Finally, (p)ppGpp-driven reprogramming induces antimicrobial tolerance, particularly under biofilm conditions, independently of its effects on growth.
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.