Cargando…

Films of Bacteria at Interfaces (FBI): Remodeling of Fluid Interfaces by Pseudomonas aeruginosa

Bacteria at fluid interfaces endure physical and chemical stresses unique to these highly asymmetric environments. The responses of Pseudomonas aeruginosa PAO1 and PA14 to a hexadecane-water interface are compared. PAO1 cells form elastic films of bacteria, excreted polysaccharides and proteins, whe...

Descripción completa

Detalles Bibliográficos
Autores principales: Niepa, Tagbo H. R., Vaccari, Liana, Leheny, Robert L., Goulian, Mark, Lee, Daeyeon, Stebe, Kathleen J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736630/
https://www.ncbi.nlm.nih.gov/pubmed/29259206
http://dx.doi.org/10.1038/s41598-017-17721-3
_version_ 1783287393135099904
author Niepa, Tagbo H. R.
Vaccari, Liana
Leheny, Robert L.
Goulian, Mark
Lee, Daeyeon
Stebe, Kathleen J.
author_facet Niepa, Tagbo H. R.
Vaccari, Liana
Leheny, Robert L.
Goulian, Mark
Lee, Daeyeon
Stebe, Kathleen J.
author_sort Niepa, Tagbo H. R.
collection PubMed
description Bacteria at fluid interfaces endure physical and chemical stresses unique to these highly asymmetric environments. The responses of Pseudomonas aeruginosa PAO1 and PA14 to a hexadecane-water interface are compared. PAO1 cells form elastic films of bacteria, excreted polysaccharides and proteins, whereas PA14 cells move actively without forming an elastic film. Studies of PAO1 mutants show that, unlike solid-supported biofilms, elastic interfacial film formation occurs in the absence of flagella, pili, or certain polysaccharides. Highly induced genes identified in transcriptional profiling include those for putative enzymes and a carbohydrate metabolism enzyme, alkB2; this latter gene is not upregulated in PA14 cells. Notably, PAO1 mutants lacking the alkB2 gene fail to form an elastic layer. Rather, they form an active film like that formed by PA14. These findings demonstrate that genetic expression is altered by interfacial confinement, and suggest that the ability to metabolize alkanes may play a role in elastic film formation at oil-water interfaces.
format Online
Article
Text
id pubmed-5736630
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-57366302017-12-21 Films of Bacteria at Interfaces (FBI): Remodeling of Fluid Interfaces by Pseudomonas aeruginosa Niepa, Tagbo H. R. Vaccari, Liana Leheny, Robert L. Goulian, Mark Lee, Daeyeon Stebe, Kathleen J. Sci Rep Article Bacteria at fluid interfaces endure physical and chemical stresses unique to these highly asymmetric environments. The responses of Pseudomonas aeruginosa PAO1 and PA14 to a hexadecane-water interface are compared. PAO1 cells form elastic films of bacteria, excreted polysaccharides and proteins, whereas PA14 cells move actively without forming an elastic film. Studies of PAO1 mutants show that, unlike solid-supported biofilms, elastic interfacial film formation occurs in the absence of flagella, pili, or certain polysaccharides. Highly induced genes identified in transcriptional profiling include those for putative enzymes and a carbohydrate metabolism enzyme, alkB2; this latter gene is not upregulated in PA14 cells. Notably, PAO1 mutants lacking the alkB2 gene fail to form an elastic layer. Rather, they form an active film like that formed by PA14. These findings demonstrate that genetic expression is altered by interfacial confinement, and suggest that the ability to metabolize alkanes may play a role in elastic film formation at oil-water interfaces. Nature Publishing Group UK 2017-12-19 /pmc/articles/PMC5736630/ /pubmed/29259206 http://dx.doi.org/10.1038/s41598-017-17721-3 Text en © The Author(s) 2017 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
Niepa, Tagbo H. R.
Vaccari, Liana
Leheny, Robert L.
Goulian, Mark
Lee, Daeyeon
Stebe, Kathleen J.
Films of Bacteria at Interfaces (FBI): Remodeling of Fluid Interfaces by Pseudomonas aeruginosa
title Films of Bacteria at Interfaces (FBI): Remodeling of Fluid Interfaces by Pseudomonas aeruginosa
title_full Films of Bacteria at Interfaces (FBI): Remodeling of Fluid Interfaces by Pseudomonas aeruginosa
title_fullStr Films of Bacteria at Interfaces (FBI): Remodeling of Fluid Interfaces by Pseudomonas aeruginosa
title_full_unstemmed Films of Bacteria at Interfaces (FBI): Remodeling of Fluid Interfaces by Pseudomonas aeruginosa
title_short Films of Bacteria at Interfaces (FBI): Remodeling of Fluid Interfaces by Pseudomonas aeruginosa
title_sort films of bacteria at interfaces (fbi): remodeling of fluid interfaces by pseudomonas aeruginosa
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736630/
https://www.ncbi.nlm.nih.gov/pubmed/29259206
http://dx.doi.org/10.1038/s41598-017-17721-3
work_keys_str_mv AT niepatagbohr filmsofbacteriaatinterfacesfbiremodelingoffluidinterfacesbypseudomonasaeruginosa
AT vaccariliana filmsofbacteriaatinterfacesfbiremodelingoffluidinterfacesbypseudomonasaeruginosa
AT lehenyrobertl filmsofbacteriaatinterfacesfbiremodelingoffluidinterfacesbypseudomonasaeruginosa
AT goulianmark filmsofbacteriaatinterfacesfbiremodelingoffluidinterfacesbypseudomonasaeruginosa
AT leedaeyeon filmsofbacteriaatinterfacesfbiremodelingoffluidinterfacesbypseudomonasaeruginosa
AT stebekathleenj filmsofbacteriaatinterfacesfbiremodelingoffluidinterfacesbypseudomonasaeruginosa