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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shared Science Publishers OG
2015
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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. |
format | Online Article Text |
id | pubmed-5354590 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Shared Science Publishers OG |
record_format | MEDLINE/PubMed |
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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