Cargando…

Two new siderophores produced by Pseudomonas sp. NCIMB 10586: The anti-oomycete non-ribosomal peptide synthetase-dependent mupirochelin and the NRPS-independent triabactin

INTRODUCTION: Globisporangium ultimum is an oomycetal pathogen causing damping-off on over 300 different plant hosts. Currently, as for many phytopathogens, its control relies in the use of chemicals with negative impact on health and ecosystems. Therefore, many biocontrol strategies are under inves...

Descripción completa

Detalles Bibliográficos
Autores principales: Grosse, Camille, Brandt, Nathalie, Van Antwerpen, Pierre, Wintjens, René, Matthijs, Sandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10080011/
https://www.ncbi.nlm.nih.gov/pubmed/37032897
http://dx.doi.org/10.3389/fmicb.2023.1143861
_version_ 1785020831090343936
author Grosse, Camille
Brandt, Nathalie
Van Antwerpen, Pierre
Wintjens, René
Matthijs, Sandra
author_facet Grosse, Camille
Brandt, Nathalie
Van Antwerpen, Pierre
Wintjens, René
Matthijs, Sandra
author_sort Grosse, Camille
collection PubMed
description INTRODUCTION: Globisporangium ultimum is an oomycetal pathogen causing damping-off on over 300 different plant hosts. Currently, as for many phytopathogens, its control relies in the use of chemicals with negative impact on health and ecosystems. Therefore, many biocontrol strategies are under investigation to reduce the use of fungicides. RESULTS: In this study, the soil bacterium Pseudomonas sp. NCIMB 10586 demonstrates a strong iron-repressed in vitro antagonism against G. ultimum MUCL 38045. This antagonism does not depend on the secretion of the broad-range antibiotic mupirocin or of the siderophore pyoverdine by the bacterial strain. The inhibitor molecule was identified as a novel non-ribosomal peptide synthetase (NRPS) siderophore named mupirochelin. Its putative structure bears similarities to other siderophores and bioactive compounds. The transcription of its gene cluster is affected by the biosynthesis of pyoverdine, the major known siderophore of the strain. Besides mupirochelin, we observed the production of a third and novel NRPS-independent siderophore (NIS), here termed triabactin. The iron-responsive transcriptional repression of the two newly identified siderophore gene clusters corroborates their role as iron scavengers. However, their respective contributions to the strain fitness are dissimilar. Bacterial growth in iron-deprived conditions is greatly supported by pyoverdine production and, to a lesser extent, by triabactin. On the contrary, mupirochelin does not contribute to the strain fitness under the studied conditions. CONCLUSION: Altogether, we have demonstrated here that besides pyoverdine, Pseudomonas sp. NCIMB 10586 produces two newly identified siderophores, namely mupirochelin, a weak siderophore with strong antagonism activity against G. ultimum, and the potent siderophore triabactin.
format Online
Article
Text
id pubmed-10080011
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-100800112023-04-08 Two new siderophores produced by Pseudomonas sp. NCIMB 10586: The anti-oomycete non-ribosomal peptide synthetase-dependent mupirochelin and the NRPS-independent triabactin Grosse, Camille Brandt, Nathalie Van Antwerpen, Pierre Wintjens, René Matthijs, Sandra Front Microbiol Microbiology INTRODUCTION: Globisporangium ultimum is an oomycetal pathogen causing damping-off on over 300 different plant hosts. Currently, as for many phytopathogens, its control relies in the use of chemicals with negative impact on health and ecosystems. Therefore, many biocontrol strategies are under investigation to reduce the use of fungicides. RESULTS: In this study, the soil bacterium Pseudomonas sp. NCIMB 10586 demonstrates a strong iron-repressed in vitro antagonism against G. ultimum MUCL 38045. This antagonism does not depend on the secretion of the broad-range antibiotic mupirocin or of the siderophore pyoverdine by the bacterial strain. The inhibitor molecule was identified as a novel non-ribosomal peptide synthetase (NRPS) siderophore named mupirochelin. Its putative structure bears similarities to other siderophores and bioactive compounds. The transcription of its gene cluster is affected by the biosynthesis of pyoverdine, the major known siderophore of the strain. Besides mupirochelin, we observed the production of a third and novel NRPS-independent siderophore (NIS), here termed triabactin. The iron-responsive transcriptional repression of the two newly identified siderophore gene clusters corroborates their role as iron scavengers. However, their respective contributions to the strain fitness are dissimilar. Bacterial growth in iron-deprived conditions is greatly supported by pyoverdine production and, to a lesser extent, by triabactin. On the contrary, mupirochelin does not contribute to the strain fitness under the studied conditions. CONCLUSION: Altogether, we have demonstrated here that besides pyoverdine, Pseudomonas sp. NCIMB 10586 produces two newly identified siderophores, namely mupirochelin, a weak siderophore with strong antagonism activity against G. ultimum, and the potent siderophore triabactin. Frontiers Media S.A. 2023-03-24 /pmc/articles/PMC10080011/ /pubmed/37032897 http://dx.doi.org/10.3389/fmicb.2023.1143861 Text en Copyright © 2023 Grosse, Brandt, Van Antwerpen, Wintjens and Matthijs. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Grosse, Camille
Brandt, Nathalie
Van Antwerpen, Pierre
Wintjens, René
Matthijs, Sandra
Two new siderophores produced by Pseudomonas sp. NCIMB 10586: The anti-oomycete non-ribosomal peptide synthetase-dependent mupirochelin and the NRPS-independent triabactin
title Two new siderophores produced by Pseudomonas sp. NCIMB 10586: The anti-oomycete non-ribosomal peptide synthetase-dependent mupirochelin and the NRPS-independent triabactin
title_full Two new siderophores produced by Pseudomonas sp. NCIMB 10586: The anti-oomycete non-ribosomal peptide synthetase-dependent mupirochelin and the NRPS-independent triabactin
title_fullStr Two new siderophores produced by Pseudomonas sp. NCIMB 10586: The anti-oomycete non-ribosomal peptide synthetase-dependent mupirochelin and the NRPS-independent triabactin
title_full_unstemmed Two new siderophores produced by Pseudomonas sp. NCIMB 10586: The anti-oomycete non-ribosomal peptide synthetase-dependent mupirochelin and the NRPS-independent triabactin
title_short Two new siderophores produced by Pseudomonas sp. NCIMB 10586: The anti-oomycete non-ribosomal peptide synthetase-dependent mupirochelin and the NRPS-independent triabactin
title_sort two new siderophores produced by pseudomonas sp. ncimb 10586: the anti-oomycete non-ribosomal peptide synthetase-dependent mupirochelin and the nrps-independent triabactin
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10080011/
https://www.ncbi.nlm.nih.gov/pubmed/37032897
http://dx.doi.org/10.3389/fmicb.2023.1143861
work_keys_str_mv AT grossecamille twonewsiderophoresproducedbypseudomonasspncimb10586theantioomycetenonribosomalpeptidesynthetasedependentmupirochelinandthenrpsindependenttriabactin
AT brandtnathalie twonewsiderophoresproducedbypseudomonasspncimb10586theantioomycetenonribosomalpeptidesynthetasedependentmupirochelinandthenrpsindependenttriabactin
AT vanantwerpenpierre twonewsiderophoresproducedbypseudomonasspncimb10586theantioomycetenonribosomalpeptidesynthetasedependentmupirochelinandthenrpsindependenttriabactin
AT wintjensrene twonewsiderophoresproducedbypseudomonasspncimb10586theantioomycetenonribosomalpeptidesynthetasedependentmupirochelinandthenrpsindependenttriabactin
AT matthijssandra twonewsiderophoresproducedbypseudomonasspncimb10586theantioomycetenonribosomalpeptidesynthetasedependentmupirochelinandthenrpsindependenttriabactin