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Biofilm assembly becomes crystal clear – filamentous bacteriophage organize the Pseudomonas aeruginosa biofilm matrix into a liquid crystal

Pseudomonas aeruginosa is an opportunistic bacterial pathogen associated with many types of chronic infection. At sites of chronic infection, such as the airways of people with cystic fibrosis (CF), P. aeruginosa forms biofilm-like aggregates. These are clusters of bacterial cells encased in a polym...

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Autores principales: Secor, Patrick R., Jennings, Laura K., Michaels, Lia A., Sweere, Johanna M., Singh, Pradeep K., Parks, William C., Bollyky, Paul L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shared Science Publishers OG 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354590/
https://www.ncbi.nlm.nih.gov/pubmed/28357315
http://dx.doi.org/10.15698/mic2016.01.475
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author Secor, Patrick R.
Jennings, Laura K.
Michaels, Lia A.
Sweere, Johanna M.
Singh, Pradeep K.
Parks, William C.
Bollyky, Paul L.
author_facet Secor, Patrick R.
Jennings, Laura K.
Michaels, Lia A.
Sweere, Johanna M.
Singh, Pradeep K.
Parks, William C.
Bollyky, Paul L.
author_sort Secor, Patrick R.
collection PubMed
description Pseudomonas aeruginosa is an opportunistic bacterial pathogen associated with many types of chronic infection. At sites of chronic infection, such as the airways of people with cystic fibrosis (CF), P. aeruginosa forms biofilm-like aggregates. These are clusters of bacterial cells encased in a polymer-rich matrix that shields bacteria from environmental stresses and antibiotic treatment. When P. aeruginosa forms a biofilm, large amounts of filamentous Pf bacteriophage (phage) are produced. Unlike most phage that typically lyse and kill their bacterial hosts, filamentous phage of the genus Inovirus, which includes Pf phage, often do not, and instead are continuously extruded from the bacteria. Here, we discuss the implications of the accumulation of filamentous Pf phage in the biofilm matrix, where they interact with matrix polymers to organize the biofilm into a highly ordered liquid crystal. This structural configuration promotes bacterial adhesion, desiccation survival, and antibiotic tolerance – all features typically associated with biofilms. We propose that Pf phage make structural contributions to P. aeruginosa biofilms and that this constitutes a novel form of symbiosis between bacteria and bacteriophage.
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spelling pubmed-53545902017-03-29 Biofilm assembly becomes crystal clear – filamentous bacteriophage organize the Pseudomonas aeruginosa biofilm matrix into a liquid crystal Secor, Patrick R. Jennings, Laura K. Michaels, Lia A. Sweere, Johanna M. Singh, Pradeep K. Parks, William C. Bollyky, Paul L. Microb Cell Microbiology Pseudomonas aeruginosa is an opportunistic bacterial pathogen associated with many types of chronic infection. At sites of chronic infection, such as the airways of people with cystic fibrosis (CF), P. aeruginosa forms biofilm-like aggregates. These are clusters of bacterial cells encased in a polymer-rich matrix that shields bacteria from environmental stresses and antibiotic treatment. When P. aeruginosa forms a biofilm, large amounts of filamentous Pf bacteriophage (phage) are produced. Unlike most phage that typically lyse and kill their bacterial hosts, filamentous phage of the genus Inovirus, which includes Pf phage, often do not, and instead are continuously extruded from the bacteria. Here, we discuss the implications of the accumulation of filamentous Pf phage in the biofilm matrix, where they interact with matrix polymers to organize the biofilm into a highly ordered liquid crystal. This structural configuration promotes bacterial adhesion, desiccation survival, and antibiotic tolerance – all features typically associated with biofilms. We propose that Pf phage make structural contributions to P. aeruginosa biofilms and that this constitutes a novel form of symbiosis between bacteria and bacteriophage. Shared Science Publishers OG 2015-12-31 /pmc/articles/PMC5354590/ /pubmed/28357315 http://dx.doi.org/10.15698/mic2016.01.475 Text en https://creativecommons.org/licenses/by/4.0/ This is an open-access article released under the terms of the Creative Commons Attribution (CC BY) license, which allows the unrestricted use, distribution, and reproduction in any medium, provided the original author and source are acknowledged.
spellingShingle Microbiology
Secor, Patrick R.
Jennings, Laura K.
Michaels, Lia A.
Sweere, Johanna M.
Singh, Pradeep K.
Parks, William C.
Bollyky, Paul L.
Biofilm assembly becomes crystal clear – filamentous bacteriophage organize the Pseudomonas aeruginosa biofilm matrix into a liquid crystal
title Biofilm assembly becomes crystal clear – filamentous bacteriophage organize the Pseudomonas aeruginosa biofilm matrix into a liquid crystal
title_full Biofilm assembly becomes crystal clear – filamentous bacteriophage organize the Pseudomonas aeruginosa biofilm matrix into a liquid crystal
title_fullStr Biofilm assembly becomes crystal clear – filamentous bacteriophage organize the Pseudomonas aeruginosa biofilm matrix into a liquid crystal
title_full_unstemmed Biofilm assembly becomes crystal clear – filamentous bacteriophage organize the Pseudomonas aeruginosa biofilm matrix into a liquid crystal
title_short Biofilm assembly becomes crystal clear – filamentous bacteriophage organize the Pseudomonas aeruginosa biofilm matrix into a liquid crystal
title_sort biofilm assembly becomes crystal clear – filamentous bacteriophage organize the pseudomonas aeruginosa biofilm matrix into a liquid crystal
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354590/
https://www.ncbi.nlm.nih.gov/pubmed/28357315
http://dx.doi.org/10.15698/mic2016.01.475
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