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Pseudomonas putida mediates bacterial killing, biofilm invasion and biocontrol with a type IVB secretion system

Many bacteria utilize contact-dependent killing machineries to eliminate rivals in their environmental niches. Here we show that the plant root colonizer Pseudomonas putida strain IsoF is able to kill a wide range of soil and plant-associated Gram-negative bacteria with the aid of a type IVB secreti...

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Autores principales: Purtschert-Montenegro, Gabriela, Cárcamo-Oyarce, Gerardo, Pinto-Carbó, Marta, Agnoli, Kirsty, Bailly, Aurélien, Eberl, Leo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9519443/
https://www.ncbi.nlm.nih.gov/pubmed/36123439
http://dx.doi.org/10.1038/s41564-022-01209-6
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author Purtschert-Montenegro, Gabriela
Cárcamo-Oyarce, Gerardo
Pinto-Carbó, Marta
Agnoli, Kirsty
Bailly, Aurélien
Eberl, Leo
author_facet Purtschert-Montenegro, Gabriela
Cárcamo-Oyarce, Gerardo
Pinto-Carbó, Marta
Agnoli, Kirsty
Bailly, Aurélien
Eberl, Leo
author_sort Purtschert-Montenegro, Gabriela
collection PubMed
description Many bacteria utilize contact-dependent killing machineries to eliminate rivals in their environmental niches. Here we show that the plant root colonizer Pseudomonas putida strain IsoF is able to kill a wide range of soil and plant-associated Gram-negative bacteria with the aid of a type IVB secretion system (T4BSS) that delivers a toxic effector into bacterial competitors in a contact-dependent manner. This extends the range of targets of T4BSSs—so far thought to transfer effectors only into eukaryotic cells—to prokaryotes. Bioinformatic and genetic analyses showed that this killing machine is entirely encoded by the kib gene cluster located within a rare genomic island, which was recently acquired by horizontal gene transfer. P. putida IsoF utilizes this secretion system not only as a defensive weapon to kill bacterial competitors but also as an offensive weapon to invade existing biofilms, allowing the strain to persist in its natural environment. Furthermore, we show that strain IsoF can protect tomato plants against the phytopathogen Ralstonia solanacearum in a T4BSS-dependent manner, suggesting that IsoF can be exploited for pest control and sustainable agriculture.
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spelling pubmed-95194432022-09-30 Pseudomonas putida mediates bacterial killing, biofilm invasion and biocontrol with a type IVB secretion system Purtschert-Montenegro, Gabriela Cárcamo-Oyarce, Gerardo Pinto-Carbó, Marta Agnoli, Kirsty Bailly, Aurélien Eberl, Leo Nat Microbiol Article Many bacteria utilize contact-dependent killing machineries to eliminate rivals in their environmental niches. Here we show that the plant root colonizer Pseudomonas putida strain IsoF is able to kill a wide range of soil and plant-associated Gram-negative bacteria with the aid of a type IVB secretion system (T4BSS) that delivers a toxic effector into bacterial competitors in a contact-dependent manner. This extends the range of targets of T4BSSs—so far thought to transfer effectors only into eukaryotic cells—to prokaryotes. Bioinformatic and genetic analyses showed that this killing machine is entirely encoded by the kib gene cluster located within a rare genomic island, which was recently acquired by horizontal gene transfer. P. putida IsoF utilizes this secretion system not only as a defensive weapon to kill bacterial competitors but also as an offensive weapon to invade existing biofilms, allowing the strain to persist in its natural environment. Furthermore, we show that strain IsoF can protect tomato plants against the phytopathogen Ralstonia solanacearum in a T4BSS-dependent manner, suggesting that IsoF can be exploited for pest control and sustainable agriculture. Nature Publishing Group UK 2022-09-19 2022 /pmc/articles/PMC9519443/ /pubmed/36123439 http://dx.doi.org/10.1038/s41564-022-01209-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Purtschert-Montenegro, Gabriela
Cárcamo-Oyarce, Gerardo
Pinto-Carbó, Marta
Agnoli, Kirsty
Bailly, Aurélien
Eberl, Leo
Pseudomonas putida mediates bacterial killing, biofilm invasion and biocontrol with a type IVB secretion system
title Pseudomonas putida mediates bacterial killing, biofilm invasion and biocontrol with a type IVB secretion system
title_full Pseudomonas putida mediates bacterial killing, biofilm invasion and biocontrol with a type IVB secretion system
title_fullStr Pseudomonas putida mediates bacterial killing, biofilm invasion and biocontrol with a type IVB secretion system
title_full_unstemmed Pseudomonas putida mediates bacterial killing, biofilm invasion and biocontrol with a type IVB secretion system
title_short Pseudomonas putida mediates bacterial killing, biofilm invasion and biocontrol with a type IVB secretion system
title_sort pseudomonas putida mediates bacterial killing, biofilm invasion and biocontrol with a type ivb secretion system
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9519443/
https://www.ncbi.nlm.nih.gov/pubmed/36123439
http://dx.doi.org/10.1038/s41564-022-01209-6
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