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Cytotoxic rhamnolipid micelles drive acute virulence in Pseudomonas aeruginosa
Pseudomonas aeruginosa is an opportunistic human pathogen that has developed multi- or even pan-drug resistance towards most frontline and last resort antibiotics, leading to increasing infections and deaths among hospitalized patients, especially those with compromised immune systems. Further compl...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10592815/ https://www.ncbi.nlm.nih.gov/pubmed/37873290 http://dx.doi.org/10.1101/2023.10.13.562257 |
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author | Xu, Qi Kang, Donghoon Meyer, Matthew D. Pennington, Christopher L. Gopal, Citrupa Schertzer, Jeffrey W. Kirienko, Natalia V. |
author_facet | Xu, Qi Kang, Donghoon Meyer, Matthew D. Pennington, Christopher L. Gopal, Citrupa Schertzer, Jeffrey W. Kirienko, Natalia V. |
author_sort | Xu, Qi |
collection | PubMed |
description | Pseudomonas aeruginosa is an opportunistic human pathogen that has developed multi- or even pan-drug resistance towards most frontline and last resort antibiotics, leading to increasing infections and deaths among hospitalized patients, especially those with compromised immune systems. Further complicating treatment, P. aeruginosa produces numerous virulence factors that contribute to host tissue damage and immune evasion, promoting bacterial colonization and pathogenesis. In this study, we demonstrate the importance of rhamnolipid production in host-pathogen interactions. Secreted rhamnolipids form micelles that exhibited highly acute toxicity towards murine macrophages, rupturing the plasma membrane and causing organellar membrane damage within minutes of exposure. While rhamnolipid micelles (RMs) were particularly toxic to macrophages, they also caused membrane damage in human lung epithelial cells, red blood cells, Gram-positive bacteria, and even non-cellular models like giant plasma membrane vesicles. Most importantly, rhamnolipid production strongly correlated to P. aeruginosa virulence against murine macrophages in various panels of clinical isolates. Altogether, our findings suggest that rhamnolipid micelles are highly cytotoxic virulence factors that drive acute cellular damage and immune evasion during P. aeruginosa infections. |
format | Online Article Text |
id | pubmed-10592815 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-105928152023-10-24 Cytotoxic rhamnolipid micelles drive acute virulence in Pseudomonas aeruginosa Xu, Qi Kang, Donghoon Meyer, Matthew D. Pennington, Christopher L. Gopal, Citrupa Schertzer, Jeffrey W. Kirienko, Natalia V. bioRxiv Article Pseudomonas aeruginosa is an opportunistic human pathogen that has developed multi- or even pan-drug resistance towards most frontline and last resort antibiotics, leading to increasing infections and deaths among hospitalized patients, especially those with compromised immune systems. Further complicating treatment, P. aeruginosa produces numerous virulence factors that contribute to host tissue damage and immune evasion, promoting bacterial colonization and pathogenesis. In this study, we demonstrate the importance of rhamnolipid production in host-pathogen interactions. Secreted rhamnolipids form micelles that exhibited highly acute toxicity towards murine macrophages, rupturing the plasma membrane and causing organellar membrane damage within minutes of exposure. While rhamnolipid micelles (RMs) were particularly toxic to macrophages, they also caused membrane damage in human lung epithelial cells, red blood cells, Gram-positive bacteria, and even non-cellular models like giant plasma membrane vesicles. Most importantly, rhamnolipid production strongly correlated to P. aeruginosa virulence against murine macrophages in various panels of clinical isolates. Altogether, our findings suggest that rhamnolipid micelles are highly cytotoxic virulence factors that drive acute cellular damage and immune evasion during P. aeruginosa infections. Cold Spring Harbor Laboratory 2023-10-13 /pmc/articles/PMC10592815/ /pubmed/37873290 http://dx.doi.org/10.1101/2023.10.13.562257 Text en https://creativecommons.org/licenses/by-nd/4.0/This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, and only so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Xu, Qi Kang, Donghoon Meyer, Matthew D. Pennington, Christopher L. Gopal, Citrupa Schertzer, Jeffrey W. Kirienko, Natalia V. Cytotoxic rhamnolipid micelles drive acute virulence in Pseudomonas aeruginosa |
title | Cytotoxic rhamnolipid micelles drive acute virulence in Pseudomonas aeruginosa |
title_full | Cytotoxic rhamnolipid micelles drive acute virulence in Pseudomonas aeruginosa |
title_fullStr | Cytotoxic rhamnolipid micelles drive acute virulence in Pseudomonas aeruginosa |
title_full_unstemmed | Cytotoxic rhamnolipid micelles drive acute virulence in Pseudomonas aeruginosa |
title_short | Cytotoxic rhamnolipid micelles drive acute virulence in Pseudomonas aeruginosa |
title_sort | cytotoxic rhamnolipid micelles drive acute virulence in pseudomonas aeruginosa |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10592815/ https://www.ncbi.nlm.nih.gov/pubmed/37873290 http://dx.doi.org/10.1101/2023.10.13.562257 |
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