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The great divide: rhamnolipids mediate separation between P. aeruginosa and S. aureus

The interactions between bacterial species during infection can have significant impacts on pathogenesis. Pseudomonas aeruginosa and Staphylococcus aureus are opportunistic bacterial pathogens that can co-infect hosts and cause serious illness. The factors that dictate whether one species outcompete...

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Autores principales: Bru, Jean-Louis, Kasallis, Summer J., Chang, Rendell, Zhuo, Quantum, Nguyen, Jacqueline, Pham, Phillip, Warren, Elizabeth, Whiteson, Katrine, Høyland-Kroghsbo, Nina Molin, Limoli, Dominique H., Siryaporn, Albert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10540625/
https://www.ncbi.nlm.nih.gov/pubmed/37780859
http://dx.doi.org/10.3389/fcimb.2023.1245874
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author Bru, Jean-Louis
Kasallis, Summer J.
Chang, Rendell
Zhuo, Quantum
Nguyen, Jacqueline
Pham, Phillip
Warren, Elizabeth
Whiteson, Katrine
Høyland-Kroghsbo, Nina Molin
Limoli, Dominique H.
Siryaporn, Albert
author_facet Bru, Jean-Louis
Kasallis, Summer J.
Chang, Rendell
Zhuo, Quantum
Nguyen, Jacqueline
Pham, Phillip
Warren, Elizabeth
Whiteson, Katrine
Høyland-Kroghsbo, Nina Molin
Limoli, Dominique H.
Siryaporn, Albert
author_sort Bru, Jean-Louis
collection PubMed
description The interactions between bacterial species during infection can have significant impacts on pathogenesis. Pseudomonas aeruginosa and Staphylococcus aureus are opportunistic bacterial pathogens that can co-infect hosts and cause serious illness. The factors that dictate whether one species outcompetes the other or whether the two species coexist are not fully understood. We investigated the role of surfactants in the interactions between these two species on a surface that enables P. aeruginosa to swarm. We found that P. aeruginosa swarms are repelled by colonies of clinical S. aureus isolates, creating physical separation between the two strains. This effect was abolished in mutants of S. aureus that were defective in the production of phenol-soluble modulins (PSMs), which form amyloid fibrils around wild-type S. aureus colonies. We investigated the mechanism that establishes physical separation between the two species using Imaging of Reflected Illuminated Structures (IRIS), which is a non-invasive imaging method that tracks the flow of surfactants produced by P. aeruginosa. We found that PSMs produced by S. aureus deflected the surfactant flow, which in turn, altered the direction of P. aeruginosa swarms. These findings show that rhamnolipids mediate physical separation between P. aeruginosa and S. aureus, which could facilitate coexistence between these species. Additionally, we found that a number of molecules repelled P. aeruginosa swarms, consistent with a surfactant deflection mechanism. These include Bacillus subtilis surfactant, the fatty acids oleic acid and linoleic acid, and the synthetic lubricant polydimethylsiloxane. Lung surfactant repelled P. aeruginosa swarms and inhibited swarm expansion altogether at higher concentration. Our results suggest that surfactant interactions could have major impacts on bacteria-bacteria and bacteria-host relationships. In addition, our findings uncover a mechanism responsible for P. aeruginosa swarm development that does not rely solely on sensing but instead is based on the flow of surfactant.
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spelling pubmed-105406252023-09-30 The great divide: rhamnolipids mediate separation between P. aeruginosa and S. aureus Bru, Jean-Louis Kasallis, Summer J. Chang, Rendell Zhuo, Quantum Nguyen, Jacqueline Pham, Phillip Warren, Elizabeth Whiteson, Katrine Høyland-Kroghsbo, Nina Molin Limoli, Dominique H. Siryaporn, Albert Front Cell Infect Microbiol Cellular and Infection Microbiology The interactions between bacterial species during infection can have significant impacts on pathogenesis. Pseudomonas aeruginosa and Staphylococcus aureus are opportunistic bacterial pathogens that can co-infect hosts and cause serious illness. The factors that dictate whether one species outcompetes the other or whether the two species coexist are not fully understood. We investigated the role of surfactants in the interactions between these two species on a surface that enables P. aeruginosa to swarm. We found that P. aeruginosa swarms are repelled by colonies of clinical S. aureus isolates, creating physical separation between the two strains. This effect was abolished in mutants of S. aureus that were defective in the production of phenol-soluble modulins (PSMs), which form amyloid fibrils around wild-type S. aureus colonies. We investigated the mechanism that establishes physical separation between the two species using Imaging of Reflected Illuminated Structures (IRIS), which is a non-invasive imaging method that tracks the flow of surfactants produced by P. aeruginosa. We found that PSMs produced by S. aureus deflected the surfactant flow, which in turn, altered the direction of P. aeruginosa swarms. These findings show that rhamnolipids mediate physical separation between P. aeruginosa and S. aureus, which could facilitate coexistence between these species. Additionally, we found that a number of molecules repelled P. aeruginosa swarms, consistent with a surfactant deflection mechanism. These include Bacillus subtilis surfactant, the fatty acids oleic acid and linoleic acid, and the synthetic lubricant polydimethylsiloxane. Lung surfactant repelled P. aeruginosa swarms and inhibited swarm expansion altogether at higher concentration. Our results suggest that surfactant interactions could have major impacts on bacteria-bacteria and bacteria-host relationships. In addition, our findings uncover a mechanism responsible for P. aeruginosa swarm development that does not rely solely on sensing but instead is based on the flow of surfactant. Frontiers Media S.A. 2023-09-15 /pmc/articles/PMC10540625/ /pubmed/37780859 http://dx.doi.org/10.3389/fcimb.2023.1245874 Text en Copyright © 2023 Bru, Kasallis, Chang, Zhuo, Nguyen, Pham, Warren, Whiteson, Høyland-Kroghsbo, Limoli and Siryaporn 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 Cellular and Infection Microbiology
Bru, Jean-Louis
Kasallis, Summer J.
Chang, Rendell
Zhuo, Quantum
Nguyen, Jacqueline
Pham, Phillip
Warren, Elizabeth
Whiteson, Katrine
Høyland-Kroghsbo, Nina Molin
Limoli, Dominique H.
Siryaporn, Albert
The great divide: rhamnolipids mediate separation between P. aeruginosa and S. aureus
title The great divide: rhamnolipids mediate separation between P. aeruginosa and S. aureus
title_full The great divide: rhamnolipids mediate separation between P. aeruginosa and S. aureus
title_fullStr The great divide: rhamnolipids mediate separation between P. aeruginosa and S. aureus
title_full_unstemmed The great divide: rhamnolipids mediate separation between P. aeruginosa and S. aureus
title_short The great divide: rhamnolipids mediate separation between P. aeruginosa and S. aureus
title_sort great divide: rhamnolipids mediate separation between p. aeruginosa and s. aureus
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10540625/
https://www.ncbi.nlm.nih.gov/pubmed/37780859
http://dx.doi.org/10.3389/fcimb.2023.1245874
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