David M. Brinkley, Savannah K. Bertolli, Larry A. Gallagher, Yongjun Tan, Minola Motha de Silva, Ainsley Brockman, Dapeng Zhang, S. Brook Peterson, Joseph D. Mougous
{"title":"假单胞菌通过一个单一的调节系统协调对病毒和细菌的先天防御","authors":"David M. Brinkley, Savannah K. Bertolli, Larry A. Gallagher, Yongjun Tan, Minola Motha de Silva, Ainsley Brockman, Dapeng Zhang, S. Brook Peterson, Joseph D. Mougous","doi":"10.1016/j.chom.2025.07.016","DOIUrl":null,"url":null,"abstract":"Bacterial cells live under constant existential threats imposed by other bacteria and viruses. Mechanisms for contending with these threats are well documented; however, the regulation of these diverse defense elements remains poorly understood. Here, we describe a genome-wide, coordinated, and highly effective immune response, termed <em>G</em>ac/Rsm-regulated <em>u</em>nified <em>a</em>ntagonism <em>r</em>esponse and <em>d</em>efense (GUARD), that protects against bacterial and viral threats using a single regulatory pathway. Bioinformatic analyses reveal a <em>Pseudomonas</em>-wide form of the Gac/Rsm regulatory pathway (GRP), an established danger-sensing system in <em>P. aeruginosa</em>. Proteomic studies of diverse <em>Pseudomonas</em> species show that the pathway regulates a large and variable suite of factors implicated in defense against both bacterial and phage threats. Focusing on <em>P. protegens</em>, we identify profound phenotypic consequences of these factors against multiple forms of bacterial antagonism and several phages. Together, our results reveal that bacteria, like multicellular eukaryotes, couple danger sensing to the activation of an immune response with antibacterial and antiviral arms.","PeriodicalId":9693,"journal":{"name":"Cell host & microbe","volume":"37 1","pages":""},"PeriodicalIF":18.7000,"publicationDate":"2025-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Pseudomonads coordinate innate defense against viruses and bacteria with a single regulatory system\",\"authors\":\"David M. Brinkley, Savannah K. Bertolli, Larry A. Gallagher, Yongjun Tan, Minola Motha de Silva, Ainsley Brockman, Dapeng Zhang, S. Brook Peterson, Joseph D. Mougous\",\"doi\":\"10.1016/j.chom.2025.07.016\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Bacterial cells live under constant existential threats imposed by other bacteria and viruses. Mechanisms for contending with these threats are well documented; however, the regulation of these diverse defense elements remains poorly understood. Here, we describe a genome-wide, coordinated, and highly effective immune response, termed <em>G</em>ac/Rsm-regulated <em>u</em>nified <em>a</em>ntagonism <em>r</em>esponse and <em>d</em>efense (GUARD), that protects against bacterial and viral threats using a single regulatory pathway. Bioinformatic analyses reveal a <em>Pseudomonas</em>-wide form of the Gac/Rsm regulatory pathway (GRP), an established danger-sensing system in <em>P. aeruginosa</em>. Proteomic studies of diverse <em>Pseudomonas</em> species show that the pathway regulates a large and variable suite of factors implicated in defense against both bacterial and phage threats. Focusing on <em>P. protegens</em>, we identify profound phenotypic consequences of these factors against multiple forms of bacterial antagonism and several phages. Together, our results reveal that bacteria, like multicellular eukaryotes, couple danger sensing to the activation of an immune response with antibacterial and antiviral arms.\",\"PeriodicalId\":9693,\"journal\":{\"name\":\"Cell host & microbe\",\"volume\":\"37 1\",\"pages\":\"\"},\"PeriodicalIF\":18.7000,\"publicationDate\":\"2025-08-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cell host & microbe\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.chom.2025.07.016\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell host & microbe","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.chom.2025.07.016","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
Pseudomonads coordinate innate defense against viruses and bacteria with a single regulatory system
Bacterial cells live under constant existential threats imposed by other bacteria and viruses. Mechanisms for contending with these threats are well documented; however, the regulation of these diverse defense elements remains poorly understood. Here, we describe a genome-wide, coordinated, and highly effective immune response, termed Gac/Rsm-regulated unified antagonism response and defense (GUARD), that protects against bacterial and viral threats using a single regulatory pathway. Bioinformatic analyses reveal a Pseudomonas-wide form of the Gac/Rsm regulatory pathway (GRP), an established danger-sensing system in P. aeruginosa. Proteomic studies of diverse Pseudomonas species show that the pathway regulates a large and variable suite of factors implicated in defense against both bacterial and phage threats. Focusing on P. protegens, we identify profound phenotypic consequences of these factors against multiple forms of bacterial antagonism and several phages. Together, our results reveal that bacteria, like multicellular eukaryotes, couple danger sensing to the activation of an immune response with antibacterial and antiviral arms.
期刊介绍:
Cell Host & Microbe is a scientific journal that was launched in March 2007. The journal aims to provide a platform for scientists to exchange ideas and concepts related to the study of microbes and their interaction with host organisms at a molecular, cellular, and immune level. It publishes novel findings on a wide range of microorganisms including bacteria, fungi, parasites, and viruses. The journal focuses on the interface between the microbe and its host, whether the host is a vertebrate, invertebrate, or plant, and whether the microbe is pathogenic, non-pathogenic, or commensal. The integrated study of microbes and their interactions with each other, their host, and the cellular environment they inhabit is a unifying theme of the journal. The published work in Cell Host & Microbe is expected to be of exceptional significance within its field and also of interest to researchers in other areas. In addition to primary research articles, the journal features expert analysis, commentary, and reviews on current topics of interest in the field.