Cargando…

Biophysical and proteomic analyses of Pseudomonas syringae pv. tomato DC3000 extracellular vesicles suggest adaptive functions during plant infection

Vesiculation is a process employed by Gram-negative bacteria to release extracellular vesicles (EVs) into the environment. EVs from pathogenic bacteria play functions in host immune modulation, elimination of host defenses, and acquisition of nutrients from the host. Here, we observed EV production...

Descripción completa

Detalles Bibliográficos
Autores principales: Janda, Martin, Rybak, Katarzyna, Krassini, Laura, Meng, Chen, Feitosa-Junior, Oséias, Stigliano, Egidio, Szulc, Beata, Sklenar, Jan, Menke, Frank L.H., Malone, Jacob G., Brachmann, Andreas, Klingl, Andreas, Ludwig, Christina, Robatzek, Silke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10470744/
https://www.ncbi.nlm.nih.gov/pubmed/37366628
http://dx.doi.org/10.1128/mbio.03589-22
_version_ 1785099749029838848
author Janda, Martin
Rybak, Katarzyna
Krassini, Laura
Meng, Chen
Feitosa-Junior, Oséias
Stigliano, Egidio
Szulc, Beata
Sklenar, Jan
Menke, Frank L.H.
Malone, Jacob G.
Brachmann, Andreas
Klingl, Andreas
Ludwig, Christina
Robatzek, Silke
author_facet Janda, Martin
Rybak, Katarzyna
Krassini, Laura
Meng, Chen
Feitosa-Junior, Oséias
Stigliano, Egidio
Szulc, Beata
Sklenar, Jan
Menke, Frank L.H.
Malone, Jacob G.
Brachmann, Andreas
Klingl, Andreas
Ludwig, Christina
Robatzek, Silke
author_sort Janda, Martin
collection PubMed
description Vesiculation is a process employed by Gram-negative bacteria to release extracellular vesicles (EVs) into the environment. EVs from pathogenic bacteria play functions in host immune modulation, elimination of host defenses, and acquisition of nutrients from the host. Here, we observed EV production of the bacterial speck disease causal agent, Pseudomonas syringae pv. tomato (Pto) DC3000, as outer membrane vesicle release. Mass spectrometry identified 369 proteins enriched in Pto DC3000 EVs. The EV samples contained known immunomodulatory proteins and could induce plant immune responses mediated by bacterial flagellin. Having identified two biomarkers for EV detection, we provide evidence for Pto DC3000 releasing EVs during plant infection. Bioinformatic analysis of the EV-enriched proteins suggests a role for EVs in antibiotic defense and iron acquisition. Thus, our data provide insights into the strategies this pathogen may use to develop in a plant environment. IMPORTANCE: The release of extracellular vesicles (EVs) into the environment is ubiquitous among bacteria. Vesiculation has been recognized as an important mechanism of bacterial pathogenesis and human disease but is poorly understood in phytopathogenic bacteria. Our research addresses the role of bacterial EVs in plant infection. In this work, we show that the causal agent of bacterial speck disease, Pseudomonas syringae pv. tomato, produces EVs during plant infection. Our data suggest that EVs may help the bacteria to adapt to environments, e.g., when iron could be limiting such as the plant apoplast, laying the foundation for studying the factors that phytopathogenic bacteria use to thrive in the plant environment.
format Online
Article
Text
id pubmed-10470744
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-104707442023-09-01 Biophysical and proteomic analyses of Pseudomonas syringae pv. tomato DC3000 extracellular vesicles suggest adaptive functions during plant infection Janda, Martin Rybak, Katarzyna Krassini, Laura Meng, Chen Feitosa-Junior, Oséias Stigliano, Egidio Szulc, Beata Sklenar, Jan Menke, Frank L.H. Malone, Jacob G. Brachmann, Andreas Klingl, Andreas Ludwig, Christina Robatzek, Silke mBio Research Article Vesiculation is a process employed by Gram-negative bacteria to release extracellular vesicles (EVs) into the environment. EVs from pathogenic bacteria play functions in host immune modulation, elimination of host defenses, and acquisition of nutrients from the host. Here, we observed EV production of the bacterial speck disease causal agent, Pseudomonas syringae pv. tomato (Pto) DC3000, as outer membrane vesicle release. Mass spectrometry identified 369 proteins enriched in Pto DC3000 EVs. The EV samples contained known immunomodulatory proteins and could induce plant immune responses mediated by bacterial flagellin. Having identified two biomarkers for EV detection, we provide evidence for Pto DC3000 releasing EVs during plant infection. Bioinformatic analysis of the EV-enriched proteins suggests a role for EVs in antibiotic defense and iron acquisition. Thus, our data provide insights into the strategies this pathogen may use to develop in a plant environment. IMPORTANCE: The release of extracellular vesicles (EVs) into the environment is ubiquitous among bacteria. Vesiculation has been recognized as an important mechanism of bacterial pathogenesis and human disease but is poorly understood in phytopathogenic bacteria. Our research addresses the role of bacterial EVs in plant infection. In this work, we show that the causal agent of bacterial speck disease, Pseudomonas syringae pv. tomato, produces EVs during plant infection. Our data suggest that EVs may help the bacteria to adapt to environments, e.g., when iron could be limiting such as the plant apoplast, laying the foundation for studying the factors that phytopathogenic bacteria use to thrive in the plant environment. American Society for Microbiology 2023-06-27 /pmc/articles/PMC10470744/ /pubmed/37366628 http://dx.doi.org/10.1128/mbio.03589-22 Text en Copyright © 2023 Janda et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Janda, Martin
Rybak, Katarzyna
Krassini, Laura
Meng, Chen
Feitosa-Junior, Oséias
Stigliano, Egidio
Szulc, Beata
Sklenar, Jan
Menke, Frank L.H.
Malone, Jacob G.
Brachmann, Andreas
Klingl, Andreas
Ludwig, Christina
Robatzek, Silke
Biophysical and proteomic analyses of Pseudomonas syringae pv. tomato DC3000 extracellular vesicles suggest adaptive functions during plant infection
title Biophysical and proteomic analyses of Pseudomonas syringae pv. tomato DC3000 extracellular vesicles suggest adaptive functions during plant infection
title_full Biophysical and proteomic analyses of Pseudomonas syringae pv. tomato DC3000 extracellular vesicles suggest adaptive functions during plant infection
title_fullStr Biophysical and proteomic analyses of Pseudomonas syringae pv. tomato DC3000 extracellular vesicles suggest adaptive functions during plant infection
title_full_unstemmed Biophysical and proteomic analyses of Pseudomonas syringae pv. tomato DC3000 extracellular vesicles suggest adaptive functions during plant infection
title_short Biophysical and proteomic analyses of Pseudomonas syringae pv. tomato DC3000 extracellular vesicles suggest adaptive functions during plant infection
title_sort biophysical and proteomic analyses of pseudomonas syringae pv. tomato dc3000 extracellular vesicles suggest adaptive functions during plant infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10470744/
https://www.ncbi.nlm.nih.gov/pubmed/37366628
http://dx.doi.org/10.1128/mbio.03589-22
work_keys_str_mv AT jandamartin biophysicalandproteomicanalysesofpseudomonassyringaepvtomatodc3000extracellularvesiclessuggestadaptivefunctionsduringplantinfection
AT rybakkatarzyna biophysicalandproteomicanalysesofpseudomonassyringaepvtomatodc3000extracellularvesiclessuggestadaptivefunctionsduringplantinfection
AT krassinilaura biophysicalandproteomicanalysesofpseudomonassyringaepvtomatodc3000extracellularvesiclessuggestadaptivefunctionsduringplantinfection
AT mengchen biophysicalandproteomicanalysesofpseudomonassyringaepvtomatodc3000extracellularvesiclessuggestadaptivefunctionsduringplantinfection
AT feitosajunioroseias biophysicalandproteomicanalysesofpseudomonassyringaepvtomatodc3000extracellularvesiclessuggestadaptivefunctionsduringplantinfection
AT stiglianoegidio biophysicalandproteomicanalysesofpseudomonassyringaepvtomatodc3000extracellularvesiclessuggestadaptivefunctionsduringplantinfection
AT szulcbeata biophysicalandproteomicanalysesofpseudomonassyringaepvtomatodc3000extracellularvesiclessuggestadaptivefunctionsduringplantinfection
AT sklenarjan biophysicalandproteomicanalysesofpseudomonassyringaepvtomatodc3000extracellularvesiclessuggestadaptivefunctionsduringplantinfection
AT menkefranklh biophysicalandproteomicanalysesofpseudomonassyringaepvtomatodc3000extracellularvesiclessuggestadaptivefunctionsduringplantinfection
AT malonejacobg biophysicalandproteomicanalysesofpseudomonassyringaepvtomatodc3000extracellularvesiclessuggestadaptivefunctionsduringplantinfection
AT brachmannandreas biophysicalandproteomicanalysesofpseudomonassyringaepvtomatodc3000extracellularvesiclessuggestadaptivefunctionsduringplantinfection
AT klinglandreas biophysicalandproteomicanalysesofpseudomonassyringaepvtomatodc3000extracellularvesiclessuggestadaptivefunctionsduringplantinfection
AT ludwigchristina biophysicalandproteomicanalysesofpseudomonassyringaepvtomatodc3000extracellularvesiclessuggestadaptivefunctionsduringplantinfection
AT robatzeksilke biophysicalandproteomicanalysesofpseudomonassyringaepvtomatodc3000extracellularvesiclessuggestadaptivefunctionsduringplantinfection