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Two functionally distinct heme/iron transport systems are virulence determinants of the fish pathogen Flavobacterium psychrophilum

Bacterial pathogens have a critical impact on aquaculture, a sector that accounts for half of the human fish consumption. Flavobacterium psychrophilum (phylum Bacteroidetes) is responsible for bacterial cold-water disease in salmonids worldwide. The molecular factors involved in host invasion, colon...

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Autores principales: Zhu, Yueying, Lechardeur, Delphine, Bernardet, Jean-François, Kerouault, Brigitte, Guérin, Cyprien, Rigaudeau, Dimitri, Nicolas, Pierre, Duchaud, Eric, Rochat, Tatiana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9331221/
https://www.ncbi.nlm.nih.gov/pubmed/35880611
http://dx.doi.org/10.1080/21505594.2022.2101197
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author Zhu, Yueying
Lechardeur, Delphine
Bernardet, Jean-François
Kerouault, Brigitte
Guérin, Cyprien
Rigaudeau, Dimitri
Nicolas, Pierre
Duchaud, Eric
Rochat, Tatiana
author_facet Zhu, Yueying
Lechardeur, Delphine
Bernardet, Jean-François
Kerouault, Brigitte
Guérin, Cyprien
Rigaudeau, Dimitri
Nicolas, Pierre
Duchaud, Eric
Rochat, Tatiana
author_sort Zhu, Yueying
collection PubMed
description Bacterial pathogens have a critical impact on aquaculture, a sector that accounts for half of the human fish consumption. Flavobacterium psychrophilum (phylum Bacteroidetes) is responsible for bacterial cold-water disease in salmonids worldwide. The molecular factors involved in host invasion, colonization and haemorrhagic septicaemia are mostly unknown. In this study, we identified two new TonB-dependent receptors, HfpR and BfpR, that are required for adaptation to iron conditions encountered during infection and for virulence in rainbow trout. Transcriptional analyses revealed that their expression is tightly controlled and upregulated under specific iron sources and concentrations. Characterization of deletion mutants showed that they act without redundancy: BfpR is required for optimal growth in the presence of high haemoglobin level, while HfpR confers the capacity to acquire nutrient iron from haem or haemoglobin under iron scarcity. The gene hfpY, co-transcribed with hfpR, encodes a protein related to the HmuY family. We demonstrated that HfpY binds haem and contributes significantly to host colonization and disease severity. Overall, these results are consistent with a model in which both BfpR and Hfp systems promote haem uptake and respond to distinct signals to adapt iron acquisition to the different stages of pathogenesis. Our findings give insight into the molecular basis of pathogenicity of a serious pathogen belonging to the understudied family Flavobacteriaceae and point to the newly identified haem receptors as promising targets for antibacterial development.
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spelling pubmed-93312212022-07-29 Two functionally distinct heme/iron transport systems are virulence determinants of the fish pathogen Flavobacterium psychrophilum Zhu, Yueying Lechardeur, Delphine Bernardet, Jean-François Kerouault, Brigitte Guérin, Cyprien Rigaudeau, Dimitri Nicolas, Pierre Duchaud, Eric Rochat, Tatiana Virulence Research Paper Bacterial pathogens have a critical impact on aquaculture, a sector that accounts for half of the human fish consumption. Flavobacterium psychrophilum (phylum Bacteroidetes) is responsible for bacterial cold-water disease in salmonids worldwide. The molecular factors involved in host invasion, colonization and haemorrhagic septicaemia are mostly unknown. In this study, we identified two new TonB-dependent receptors, HfpR and BfpR, that are required for adaptation to iron conditions encountered during infection and for virulence in rainbow trout. Transcriptional analyses revealed that their expression is tightly controlled and upregulated under specific iron sources and concentrations. Characterization of deletion mutants showed that they act without redundancy: BfpR is required for optimal growth in the presence of high haemoglobin level, while HfpR confers the capacity to acquire nutrient iron from haem or haemoglobin under iron scarcity. The gene hfpY, co-transcribed with hfpR, encodes a protein related to the HmuY family. We demonstrated that HfpY binds haem and contributes significantly to host colonization and disease severity. Overall, these results are consistent with a model in which both BfpR and Hfp systems promote haem uptake and respond to distinct signals to adapt iron acquisition to the different stages of pathogenesis. Our findings give insight into the molecular basis of pathogenicity of a serious pathogen belonging to the understudied family Flavobacteriaceae and point to the newly identified haem receptors as promising targets for antibacterial development. Taylor & Francis 2022-07-26 /pmc/articles/PMC9331221/ /pubmed/35880611 http://dx.doi.org/10.1080/21505594.2022.2101197 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Zhu, Yueying
Lechardeur, Delphine
Bernardet, Jean-François
Kerouault, Brigitte
Guérin, Cyprien
Rigaudeau, Dimitri
Nicolas, Pierre
Duchaud, Eric
Rochat, Tatiana
Two functionally distinct heme/iron transport systems are virulence determinants of the fish pathogen Flavobacterium psychrophilum
title Two functionally distinct heme/iron transport systems are virulence determinants of the fish pathogen Flavobacterium psychrophilum
title_full Two functionally distinct heme/iron transport systems are virulence determinants of the fish pathogen Flavobacterium psychrophilum
title_fullStr Two functionally distinct heme/iron transport systems are virulence determinants of the fish pathogen Flavobacterium psychrophilum
title_full_unstemmed Two functionally distinct heme/iron transport systems are virulence determinants of the fish pathogen Flavobacterium psychrophilum
title_short Two functionally distinct heme/iron transport systems are virulence determinants of the fish pathogen Flavobacterium psychrophilum
title_sort two functionally distinct heme/iron transport systems are virulence determinants of the fish pathogen flavobacterium psychrophilum
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9331221/
https://www.ncbi.nlm.nih.gov/pubmed/35880611
http://dx.doi.org/10.1080/21505594.2022.2101197
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