Cargando…
Pseudomonas aeruginosa responds to exogenous polyunsaturated fatty acids (PUFAs) by modifying phospholipid composition, membrane permeability, and phenotypes associated with virulence
BACKGROUND: Pseudomonas aeruginosa, a common opportunistic pathogen, is known to cause infections in a variety of compromised human tissues. An emerging mechanism for microbial survival is the incorporation of exogenous fatty acids to alter the cell’s membrane phospholipid profile. With these findin...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137939/ https://www.ncbi.nlm.nih.gov/pubmed/30217149 http://dx.doi.org/10.1186/s12866-018-1259-8 |
_version_ | 1783355260944777216 |
---|---|
author | Baker, Lyssa Y. Hobby, Chelsea R. Siv, Andrew W. Bible, William C. Glennon, Michael S. Anderson, Derek M. Symes, Steven J. Giles, David K. |
author_facet | Baker, Lyssa Y. Hobby, Chelsea R. Siv, Andrew W. Bible, William C. Glennon, Michael S. Anderson, Derek M. Symes, Steven J. Giles, David K. |
author_sort | Baker, Lyssa Y. |
collection | PubMed |
description | BACKGROUND: Pseudomonas aeruginosa, a common opportunistic pathogen, is known to cause infections in a variety of compromised human tissues. An emerging mechanism for microbial survival is the incorporation of exogenous fatty acids to alter the cell’s membrane phospholipid profile. With these findings, we show that exogenous fatty acid exposure leads to changes in bacterial membrane phospholipid structure, membrane permeability, virulence phenotypes and consequent stress responses that may influence survival and persistence of Pseudomonas aeruginosa. RESULTS: Thin-layer chromatography and ultra performance liquid chromatography / ESI-mass spectrometry indicated alteration of bacterial phospholipid profiles following growth in the presence of polyunsaturated fatty acids (PUFAs) (ranging in carbon length and unsaturation). The exogenously supplied fatty acids were incorporated into the major bacterial phospholipids phosphatidylethanolamine and phosphatidylglycerol. The incorporation of fatty acids increased membrane permeability as judged by both accumulation and exclusion of ethidium bromide. Individual fatty acids were identified as modifying resistance to the cyclic peptide antibiotics polymyxin B and colistin, but not the beta-lactam imipenem. Biofilm formation was increased by several PUFAs and significant fluctuations in swimming motility were observed. CONCLUSIONS: Our results emphasize the relevance and complexity of exogenous fatty acids in the membrane physiology and pathobiology of a medically important pathogen. P. aeruginosa exhibits versatility with regard to utilization of and response to exogenous fatty acids, perhaps revealing potential strategies for prevention and control of infection. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12866-018-1259-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6137939 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61379392018-09-15 Pseudomonas aeruginosa responds to exogenous polyunsaturated fatty acids (PUFAs) by modifying phospholipid composition, membrane permeability, and phenotypes associated with virulence Baker, Lyssa Y. Hobby, Chelsea R. Siv, Andrew W. Bible, William C. Glennon, Michael S. Anderson, Derek M. Symes, Steven J. Giles, David K. BMC Microbiol Research Article BACKGROUND: Pseudomonas aeruginosa, a common opportunistic pathogen, is known to cause infections in a variety of compromised human tissues. An emerging mechanism for microbial survival is the incorporation of exogenous fatty acids to alter the cell’s membrane phospholipid profile. With these findings, we show that exogenous fatty acid exposure leads to changes in bacterial membrane phospholipid structure, membrane permeability, virulence phenotypes and consequent stress responses that may influence survival and persistence of Pseudomonas aeruginosa. RESULTS: Thin-layer chromatography and ultra performance liquid chromatography / ESI-mass spectrometry indicated alteration of bacterial phospholipid profiles following growth in the presence of polyunsaturated fatty acids (PUFAs) (ranging in carbon length and unsaturation). The exogenously supplied fatty acids were incorporated into the major bacterial phospholipids phosphatidylethanolamine and phosphatidylglycerol. The incorporation of fatty acids increased membrane permeability as judged by both accumulation and exclusion of ethidium bromide. Individual fatty acids were identified as modifying resistance to the cyclic peptide antibiotics polymyxin B and colistin, but not the beta-lactam imipenem. Biofilm formation was increased by several PUFAs and significant fluctuations in swimming motility were observed. CONCLUSIONS: Our results emphasize the relevance and complexity of exogenous fatty acids in the membrane physiology and pathobiology of a medically important pathogen. P. aeruginosa exhibits versatility with regard to utilization of and response to exogenous fatty acids, perhaps revealing potential strategies for prevention and control of infection. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12866-018-1259-8) contains supplementary material, which is available to authorized users. BioMed Central 2018-09-14 /pmc/articles/PMC6137939/ /pubmed/30217149 http://dx.doi.org/10.1186/s12866-018-1259-8 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Baker, Lyssa Y. Hobby, Chelsea R. Siv, Andrew W. Bible, William C. Glennon, Michael S. Anderson, Derek M. Symes, Steven J. Giles, David K. Pseudomonas aeruginosa responds to exogenous polyunsaturated fatty acids (PUFAs) by modifying phospholipid composition, membrane permeability, and phenotypes associated with virulence |
title | Pseudomonas aeruginosa responds to exogenous polyunsaturated fatty acids (PUFAs) by modifying phospholipid composition, membrane permeability, and phenotypes associated with virulence |
title_full | Pseudomonas aeruginosa responds to exogenous polyunsaturated fatty acids (PUFAs) by modifying phospholipid composition, membrane permeability, and phenotypes associated with virulence |
title_fullStr | Pseudomonas aeruginosa responds to exogenous polyunsaturated fatty acids (PUFAs) by modifying phospholipid composition, membrane permeability, and phenotypes associated with virulence |
title_full_unstemmed | Pseudomonas aeruginosa responds to exogenous polyunsaturated fatty acids (PUFAs) by modifying phospholipid composition, membrane permeability, and phenotypes associated with virulence |
title_short | Pseudomonas aeruginosa responds to exogenous polyunsaturated fatty acids (PUFAs) by modifying phospholipid composition, membrane permeability, and phenotypes associated with virulence |
title_sort | pseudomonas aeruginosa responds to exogenous polyunsaturated fatty acids (pufas) by modifying phospholipid composition, membrane permeability, and phenotypes associated with virulence |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137939/ https://www.ncbi.nlm.nih.gov/pubmed/30217149 http://dx.doi.org/10.1186/s12866-018-1259-8 |
work_keys_str_mv | AT bakerlyssay pseudomonasaeruginosarespondstoexogenouspolyunsaturatedfattyacidspufasbymodifyingphospholipidcompositionmembranepermeabilityandphenotypesassociatedwithvirulence AT hobbychelsear pseudomonasaeruginosarespondstoexogenouspolyunsaturatedfattyacidspufasbymodifyingphospholipidcompositionmembranepermeabilityandphenotypesassociatedwithvirulence AT sivandreww pseudomonasaeruginosarespondstoexogenouspolyunsaturatedfattyacidspufasbymodifyingphospholipidcompositionmembranepermeabilityandphenotypesassociatedwithvirulence AT biblewilliamc pseudomonasaeruginosarespondstoexogenouspolyunsaturatedfattyacidspufasbymodifyingphospholipidcompositionmembranepermeabilityandphenotypesassociatedwithvirulence AT glennonmichaels pseudomonasaeruginosarespondstoexogenouspolyunsaturatedfattyacidspufasbymodifyingphospholipidcompositionmembranepermeabilityandphenotypesassociatedwithvirulence AT andersonderekm pseudomonasaeruginosarespondstoexogenouspolyunsaturatedfattyacidspufasbymodifyingphospholipidcompositionmembranepermeabilityandphenotypesassociatedwithvirulence AT symesstevenj pseudomonasaeruginosarespondstoexogenouspolyunsaturatedfattyacidspufasbymodifyingphospholipidcompositionmembranepermeabilityandphenotypesassociatedwithvirulence AT gilesdavidk pseudomonasaeruginosarespondstoexogenouspolyunsaturatedfattyacidspufasbymodifyingphospholipidcompositionmembranepermeabilityandphenotypesassociatedwithvirulence |