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

Research output: Contribution to journalJournal articleResearchpeer-review

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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.

In: Frontiers in Cellular and Infection Microbiology, Vol. 13, 1245874, 2023.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Bru, J-L, Kasallis, SJ, Chang, R, Zhuo, Q, Nguyen, J, Pham, P, Warren, E, Whiteson, K, Høyland-Kroghsbo, NM, Limoli, DH & Siryaporn, A 2023, 'The great divide: rhamnolipids mediate separation between P. aeruginosa and S. aureus', Frontiers in Cellular and Infection Microbiology, vol. 13, 1245874. https://doi.org/10.3389/fcimb.2023.1245874

APA

Bru, J-L., Kasallis, S. J., Chang, R., Zhuo, Q., Nguyen, J., Pham, P., Warren, E., Whiteson, K., Høyland-Kroghsbo, N. M., Limoli, D. H., & Siryaporn, A. (2023). The great divide: rhamnolipids mediate separation between P. aeruginosa and S. aureus. Frontiers in Cellular and Infection Microbiology, 13, [1245874]. https://doi.org/10.3389/fcimb.2023.1245874

Vancouver

Bru J-L, Kasallis SJ, Chang R, Zhuo Q, Nguyen J, Pham P et al. The great divide: rhamnolipids mediate separation between P. aeruginosa and S. aureus. Frontiers in Cellular and Infection Microbiology. 2023;13. 1245874. https://doi.org/10.3389/fcimb.2023.1245874

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. / The great divide : rhamnolipids mediate separation between P. aeruginosa and S. aureus. In: Frontiers in Cellular and Infection Microbiology. 2023 ; Vol. 13.

Bibtex

@article{fbfcbd9743a04eaa874902a6556a6cb3,
title = "The great divide: rhamnolipids mediate separation between P. aeruginosa and S. aureus",
abstract = "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.",
keywords = "Humans, Pseudomonas aeruginosa, Staphylococcus aureus/genetics, Methicillin-Resistant Staphylococcus aureus, Staphylococcal Infections/microbiology, Biofilms, Surface-Active Agents",
author = "Jean-Louis Bru and Kasallis, {Summer J} and Rendell Chang and Quantum Zhuo and Jacqueline Nguyen and Phillip Pham and Elizabeth Warren and Katrine Whiteson and H{\o}yland-Kroghsbo, {Nina Molin} and Limoli, {Dominique H} and Albert Siryaporn",
note = "Copyright {\textcopyright} 2023 Bru, Kasallis, Chang, Zhuo, Nguyen, Pham, Warren, Whiteson, H{\o}yland-Kroghsbo, Limoli and Siryaporn.",
year = "2023",
doi = "10.3389/fcimb.2023.1245874",
language = "English",
volume = "13",
journal = "Frontiers in Cellular and Infection Microbiology",
issn = "2235-2988",
publisher = "Frontiers Media S.A.",

}

RIS

TY - JOUR

T1 - The great divide

T2 - rhamnolipids mediate separation between P. aeruginosa and S. aureus

AU - Bru, Jean-Louis

AU - Kasallis, Summer J

AU - Chang, Rendell

AU - Zhuo, Quantum

AU - Nguyen, Jacqueline

AU - Pham, Phillip

AU - Warren, Elizabeth

AU - Whiteson, Katrine

AU - Høyland-Kroghsbo, Nina Molin

AU - Limoli, Dominique H

AU - Siryaporn, Albert

N1 - Copyright © 2023 Bru, Kasallis, Chang, Zhuo, Nguyen, Pham, Warren, Whiteson, Høyland-Kroghsbo, Limoli and Siryaporn.

PY - 2023

Y1 - 2023

N2 - 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.

AB - 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.

KW - Humans

KW - Pseudomonas aeruginosa

KW - Staphylococcus aureus/genetics

KW - Methicillin-Resistant Staphylococcus aureus

KW - Staphylococcal Infections/microbiology

KW - Biofilms

KW - Surface-Active Agents

U2 - 10.3389/fcimb.2023.1245874

DO - 10.3389/fcimb.2023.1245874

M3 - Journal article

C2 - 37780859

VL - 13

JO - Frontiers in Cellular and Infection Microbiology

JF - Frontiers in Cellular and Infection Microbiology

SN - 2235-2988

M1 - 1245874

ER -

ID: 368679045