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Metabolic Footprints of Burkholderia Sensu Lato Rhizosphere Bacteria Active against Maize Fusarium Pathogens †

Consistent with their reported abundance in soils, several Burkholderia sensu lato strains were isolated from the rhizosphere of maize plants cultivated at different sites in central México. Comparative analysis of their 16S rRNA gene sequences permitted their separation into three distinctive clade...

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Autores principales: Barrera-Galicia, Guadalupe C., Peniche-Pavía, Héctor A., Peña-Cabriales, Juan José, Covarrubias, Sergio A., Vera-Núñez, José A., Délano-Frier, John P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8538949/
https://www.ncbi.nlm.nih.gov/pubmed/34683382
http://dx.doi.org/10.3390/microorganisms9102061
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author Barrera-Galicia, Guadalupe C.
Peniche-Pavía, Héctor A.
Peña-Cabriales, Juan José
Covarrubias, Sergio A.
Vera-Núñez, José A.
Délano-Frier, John P.
author_facet Barrera-Galicia, Guadalupe C.
Peniche-Pavía, Héctor A.
Peña-Cabriales, Juan José
Covarrubias, Sergio A.
Vera-Núñez, José A.
Délano-Frier, John P.
author_sort Barrera-Galicia, Guadalupe C.
collection PubMed
description Consistent with their reported abundance in soils, several Burkholderia sensu lato strains were isolated from the rhizosphere of maize plants cultivated at different sites in central México. Comparative analysis of their 16S rRNA gene sequences permitted their separation into three distinctive clades, which were further subdivided into six other clusters by their close resemblance to (1) Trinickia dinghuensis; (2) Paraburkholderia kirstenboschensis, P. graminis, P. dilworthii and P. rhynchosiae; (3) B. gladioli; (4) B. arboris; (5) B. contaminans, or (6) B. metallica representative species. Direct confrontation assays revealed that these strains inhibited the growth of pathogenic Fusarium oxysporum f. sp. radicis-lycopersici, and F. verticillioides within a roughly 3–55% inhibition range. The use of a DIESI-based non-targeted mass spectroscopy experimental strategy further indicated that this method is an option for rapid determination of the pathogen inhibitory capacity of Burkholderia sensu lato strains based solely on the analysis of their exometabolome. Furthermore, it showed that the highest anti-fungal activity observed in B. contaminans and B. arboris was associated with a distinctive abundance of certain m/z ions, some of which were identified as components of the ornbactin and pyochelin siderophores. These results highlight the chemical diversity of Burkholderia sensu lato bacteria and suggest that their capacity to inhibit the Fusarium-related infection of maize in suppressive soils is associated with siderophore synthesis.
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spelling pubmed-85389492021-10-24 Metabolic Footprints of Burkholderia Sensu Lato Rhizosphere Bacteria Active against Maize Fusarium Pathogens † Barrera-Galicia, Guadalupe C. Peniche-Pavía, Héctor A. Peña-Cabriales, Juan José Covarrubias, Sergio A. Vera-Núñez, José A. Délano-Frier, John P. Microorganisms Article Consistent with their reported abundance in soils, several Burkholderia sensu lato strains were isolated from the rhizosphere of maize plants cultivated at different sites in central México. Comparative analysis of their 16S rRNA gene sequences permitted their separation into three distinctive clades, which were further subdivided into six other clusters by their close resemblance to (1) Trinickia dinghuensis; (2) Paraburkholderia kirstenboschensis, P. graminis, P. dilworthii and P. rhynchosiae; (3) B. gladioli; (4) B. arboris; (5) B. contaminans, or (6) B. metallica representative species. Direct confrontation assays revealed that these strains inhibited the growth of pathogenic Fusarium oxysporum f. sp. radicis-lycopersici, and F. verticillioides within a roughly 3–55% inhibition range. The use of a DIESI-based non-targeted mass spectroscopy experimental strategy further indicated that this method is an option for rapid determination of the pathogen inhibitory capacity of Burkholderia sensu lato strains based solely on the analysis of their exometabolome. Furthermore, it showed that the highest anti-fungal activity observed in B. contaminans and B. arboris was associated with a distinctive abundance of certain m/z ions, some of which were identified as components of the ornbactin and pyochelin siderophores. These results highlight the chemical diversity of Burkholderia sensu lato bacteria and suggest that their capacity to inhibit the Fusarium-related infection of maize in suppressive soils is associated with siderophore synthesis. MDPI 2021-09-29 /pmc/articles/PMC8538949/ /pubmed/34683382 http://dx.doi.org/10.3390/microorganisms9102061 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Barrera-Galicia, Guadalupe C.
Peniche-Pavía, Héctor A.
Peña-Cabriales, Juan José
Covarrubias, Sergio A.
Vera-Núñez, José A.
Délano-Frier, John P.
Metabolic Footprints of Burkholderia Sensu Lato Rhizosphere Bacteria Active against Maize Fusarium Pathogens †
title Metabolic Footprints of Burkholderia Sensu Lato Rhizosphere Bacteria Active against Maize Fusarium Pathogens †
title_full Metabolic Footprints of Burkholderia Sensu Lato Rhizosphere Bacteria Active against Maize Fusarium Pathogens †
title_fullStr Metabolic Footprints of Burkholderia Sensu Lato Rhizosphere Bacteria Active against Maize Fusarium Pathogens †
title_full_unstemmed Metabolic Footprints of Burkholderia Sensu Lato Rhizosphere Bacteria Active against Maize Fusarium Pathogens †
title_short Metabolic Footprints of Burkholderia Sensu Lato Rhizosphere Bacteria Active against Maize Fusarium Pathogens †
title_sort metabolic footprints of burkholderia sensu lato rhizosphere bacteria active against maize fusarium pathogens †
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8538949/
https://www.ncbi.nlm.nih.gov/pubmed/34683382
http://dx.doi.org/10.3390/microorganisms9102061
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