{"title":"<i>Pseudomonas</i> cold shock proteins suppress bacterial effector translocation in <i>Nicotiana benthamiana</i>.","authors":"Shen Cong, Jun-Zhou Li, Mei-Ran Zhang, Hai-Lei Wei, Wei Zhang","doi":"10.3389/fmicb.2025.1539906","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Plants detect the invasion of microbial pathogens through pathogen-associated molecular patterns (PAMPs). Cold shock proteins (CSPs) are a class of PAMPs specifically recognized by <i>Solanales</i> plants. While peptide inoculation studies have revealed the effects of CSPs, their <i>in vivo</i> roles remain poorly understood.</p><p><strong>Methods: </strong>A model system involving the interactions between <i>Pseudomonas fluorescens</i> and <i>P. syringae</i> pv. <i>tomato</i> DC3000 with <i>Nicotiana benthamiana</i> has been widely used to investigate the molecular mechanism of plant-microbe interactions. Here, we employed this model system to explore the <i>in vivo</i> roles of CSPs in modulating plant immunity by multiple genetic approaches.</p><p><strong>Results: </strong>Our findings revealed that three highly-conserved CSPs were identified in <i>Pseudomonas</i> strains. Transient expression of these CSPs neither induced reactive oxygen species (ROS) production nor suppressed the hypersensitive response (HR) in <i>N. benthamiana</i>, however, it restricted bacterial effector translocation. Genetic analysis revealed that these CSPs did not contribute to the ROS burst or HR inhibition <i>in vivo</i> but were functionally redundant in suppressing effector translocation in a flagellin (FliC)-independent manner. Furthermore, we demonstrated that the suppression of effector translocation mediated by CSPs was less pronounced compared to that triggered by FliC. Additionally, inoculation with csp15 and csp22 epitopes triggered the pattern-triggered immunity-associated suppression of effector translocations.</p><p><strong>Discussion: </strong>This study revealed the redundant roles of CSPs in suppressing bacterial effector translocation <i>in vivo</i>, providing deep insights into the PTI elicited by cytoplasmic bacterial proteins.</p>","PeriodicalId":12466,"journal":{"name":"Frontiers in Microbiology","volume":"16 ","pages":"1539906"},"PeriodicalIF":4.0000,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11799257/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3389/fmicb.2025.1539906","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: Plants detect the invasion of microbial pathogens through pathogen-associated molecular patterns (PAMPs). Cold shock proteins (CSPs) are a class of PAMPs specifically recognized by Solanales plants. While peptide inoculation studies have revealed the effects of CSPs, their in vivo roles remain poorly understood.
Methods: A model system involving the interactions between Pseudomonas fluorescens and P. syringae pv. tomato DC3000 with Nicotiana benthamiana has been widely used to investigate the molecular mechanism of plant-microbe interactions. Here, we employed this model system to explore the in vivo roles of CSPs in modulating plant immunity by multiple genetic approaches.
Results: Our findings revealed that three highly-conserved CSPs were identified in Pseudomonas strains. Transient expression of these CSPs neither induced reactive oxygen species (ROS) production nor suppressed the hypersensitive response (HR) in N. benthamiana, however, it restricted bacterial effector translocation. Genetic analysis revealed that these CSPs did not contribute to the ROS burst or HR inhibition in vivo but were functionally redundant in suppressing effector translocation in a flagellin (FliC)-independent manner. Furthermore, we demonstrated that the suppression of effector translocation mediated by CSPs was less pronounced compared to that triggered by FliC. Additionally, inoculation with csp15 and csp22 epitopes triggered the pattern-triggered immunity-associated suppression of effector translocations.
Discussion: This study revealed the redundant roles of CSPs in suppressing bacterial effector translocation in vivo, providing deep insights into the PTI elicited by cytoplasmic bacterial proteins.
期刊介绍:
Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.