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Pseudomonas aeruginosa inhibits Rhizopus microsporus germination through sequestration of free environmental iron

Rhizopus spp are the most common etiological agents of mucormycosis, causing over 90% mortality in disseminated infection. Key to pathogenesis is the ability of fungal spores to swell, germinate, and penetrate surrounding tissues. Antibiotic treatment in at-risk patients increases the probability of...

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Autores principales: Kousser, Courtney, Clark, Callum, Sherrington, Sarah, Voelz, Kerstin, Hall, Rebecca A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6450908/
https://www.ncbi.nlm.nih.gov/pubmed/30952923
http://dx.doi.org/10.1038/s41598-019-42175-0
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author Kousser, Courtney
Clark, Callum
Sherrington, Sarah
Voelz, Kerstin
Hall, Rebecca A.
author_facet Kousser, Courtney
Clark, Callum
Sherrington, Sarah
Voelz, Kerstin
Hall, Rebecca A.
author_sort Kousser, Courtney
collection PubMed
description Rhizopus spp are the most common etiological agents of mucormycosis, causing over 90% mortality in disseminated infection. Key to pathogenesis is the ability of fungal spores to swell, germinate, and penetrate surrounding tissues. Antibiotic treatment in at-risk patients increases the probability of the patient developing mucormycosis, suggesting that bacteria have the potential to control the growth of the fungus. However, research into polymicrobial relationships involving Rhizopus spp has not been extensively explored. Here we show that co-culturing Rhizopus microsporus and Pseudomonas aeruginosa results in the inhibition of spore germination. This inhibition was mediated via the secretion of bacterial siderophores, which induced iron stress on the fungus. Addition of P. aeruginosa siderophores to R. microsporus spores in the zebrafish larval model of infection resulted in inhibition of fungal germination and reduced host mortality. Therefore, during infection antibacterial treatment may relieve bacterial imposed nutrient restriction resulting in secondary fungal infections.
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spelling pubmed-64509082019-04-10 Pseudomonas aeruginosa inhibits Rhizopus microsporus germination through sequestration of free environmental iron Kousser, Courtney Clark, Callum Sherrington, Sarah Voelz, Kerstin Hall, Rebecca A. Sci Rep Article Rhizopus spp are the most common etiological agents of mucormycosis, causing over 90% mortality in disseminated infection. Key to pathogenesis is the ability of fungal spores to swell, germinate, and penetrate surrounding tissues. Antibiotic treatment in at-risk patients increases the probability of the patient developing mucormycosis, suggesting that bacteria have the potential to control the growth of the fungus. However, research into polymicrobial relationships involving Rhizopus spp has not been extensively explored. Here we show that co-culturing Rhizopus microsporus and Pseudomonas aeruginosa results in the inhibition of spore germination. This inhibition was mediated via the secretion of bacterial siderophores, which induced iron stress on the fungus. Addition of P. aeruginosa siderophores to R. microsporus spores in the zebrafish larval model of infection resulted in inhibition of fungal germination and reduced host mortality. Therefore, during infection antibacterial treatment may relieve bacterial imposed nutrient restriction resulting in secondary fungal infections. Nature Publishing Group UK 2019-04-05 /pmc/articles/PMC6450908/ /pubmed/30952923 http://dx.doi.org/10.1038/s41598-019-42175-0 Text en © The Author(s) 2019 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/.
spellingShingle Article
Kousser, Courtney
Clark, Callum
Sherrington, Sarah
Voelz, Kerstin
Hall, Rebecca A.
Pseudomonas aeruginosa inhibits Rhizopus microsporus germination through sequestration of free environmental iron
title Pseudomonas aeruginosa inhibits Rhizopus microsporus germination through sequestration of free environmental iron
title_full Pseudomonas aeruginosa inhibits Rhizopus microsporus germination through sequestration of free environmental iron
title_fullStr Pseudomonas aeruginosa inhibits Rhizopus microsporus germination through sequestration of free environmental iron
title_full_unstemmed Pseudomonas aeruginosa inhibits Rhizopus microsporus germination through sequestration of free environmental iron
title_short Pseudomonas aeruginosa inhibits Rhizopus microsporus germination through sequestration of free environmental iron
title_sort pseudomonas aeruginosa inhibits rhizopus microsporus germination through sequestration of free environmental iron
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6450908/
https://www.ncbi.nlm.nih.gov/pubmed/30952923
http://dx.doi.org/10.1038/s41598-019-42175-0
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