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Heterogeneity in surface sensing suggests a division of labor in Pseudomonas aeruginosa populations

The second messenger signaling molecule cyclic diguanylate monophosphate (c-di-GMP) drives the transition between planktonic and biofilm growth in many bacterial species. Pseudomonas aeruginosa has two surface sensing systems that produce c-di-GMP in response to surface adherence. Current thinking i...

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Autores principales: Armbruster, Catherine R, Lee, Calvin K, Parker-Gilham, Jessica, de Anda, Jaime, Xia, Aiguo, Zhao, Kun, Murakami, Keiji, Tseng, Boo Shan, Hoffman, Lucas R, Jin, Fan, Harwood, Caroline S, Wong, Gerard CL, Parsek, Matthew R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6615863/
https://www.ncbi.nlm.nih.gov/pubmed/31180327
http://dx.doi.org/10.7554/eLife.45084
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author Armbruster, Catherine R
Lee, Calvin K
Parker-Gilham, Jessica
de Anda, Jaime
Xia, Aiguo
Zhao, Kun
Murakami, Keiji
Tseng, Boo Shan
Hoffman, Lucas R
Jin, Fan
Harwood, Caroline S
Wong, Gerard CL
Parsek, Matthew R
author_facet Armbruster, Catherine R
Lee, Calvin K
Parker-Gilham, Jessica
de Anda, Jaime
Xia, Aiguo
Zhao, Kun
Murakami, Keiji
Tseng, Boo Shan
Hoffman, Lucas R
Jin, Fan
Harwood, Caroline S
Wong, Gerard CL
Parsek, Matthew R
author_sort Armbruster, Catherine R
collection PubMed
description The second messenger signaling molecule cyclic diguanylate monophosphate (c-di-GMP) drives the transition between planktonic and biofilm growth in many bacterial species. Pseudomonas aeruginosa has two surface sensing systems that produce c-di-GMP in response to surface adherence. Current thinking in the field is that once cells attach to a surface, they uniformly respond by producing c-di-GMP. Here, we describe how the Wsp system generates heterogeneity in surface sensing, resulting in two physiologically distinct subpopulations of cells. One subpopulation has elevated c-di-GMP and produces biofilm matrix, serving as the founders of initial microcolonies. The other subpopulation has low c-di-GMP and engages in surface motility, allowing for exploration of the surface. We also show that this heterogeneity strongly correlates to surface behavior for descendent cells. Together, our results suggest that after surface attachment, P. aeruginosa engages in a division of labor that persists across generations, accelerating early biofilm formation and surface exploration.
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spelling pubmed-66158632019-07-11 Heterogeneity in surface sensing suggests a division of labor in Pseudomonas aeruginosa populations Armbruster, Catherine R Lee, Calvin K Parker-Gilham, Jessica de Anda, Jaime Xia, Aiguo Zhao, Kun Murakami, Keiji Tseng, Boo Shan Hoffman, Lucas R Jin, Fan Harwood, Caroline S Wong, Gerard CL Parsek, Matthew R eLife Microbiology and Infectious Disease The second messenger signaling molecule cyclic diguanylate monophosphate (c-di-GMP) drives the transition between planktonic and biofilm growth in many bacterial species. Pseudomonas aeruginosa has two surface sensing systems that produce c-di-GMP in response to surface adherence. Current thinking in the field is that once cells attach to a surface, they uniformly respond by producing c-di-GMP. Here, we describe how the Wsp system generates heterogeneity in surface sensing, resulting in two physiologically distinct subpopulations of cells. One subpopulation has elevated c-di-GMP and produces biofilm matrix, serving as the founders of initial microcolonies. The other subpopulation has low c-di-GMP and engages in surface motility, allowing for exploration of the surface. We also show that this heterogeneity strongly correlates to surface behavior for descendent cells. Together, our results suggest that after surface attachment, P. aeruginosa engages in a division of labor that persists across generations, accelerating early biofilm formation and surface exploration. eLife Sciences Publications, Ltd 2019-06-10 /pmc/articles/PMC6615863/ /pubmed/31180327 http://dx.doi.org/10.7554/eLife.45084 Text en © 2019, Armbruster et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Microbiology and Infectious Disease
Armbruster, Catherine R
Lee, Calvin K
Parker-Gilham, Jessica
de Anda, Jaime
Xia, Aiguo
Zhao, Kun
Murakami, Keiji
Tseng, Boo Shan
Hoffman, Lucas R
Jin, Fan
Harwood, Caroline S
Wong, Gerard CL
Parsek, Matthew R
Heterogeneity in surface sensing suggests a division of labor in Pseudomonas aeruginosa populations
title Heterogeneity in surface sensing suggests a division of labor in Pseudomonas aeruginosa populations
title_full Heterogeneity in surface sensing suggests a division of labor in Pseudomonas aeruginosa populations
title_fullStr Heterogeneity in surface sensing suggests a division of labor in Pseudomonas aeruginosa populations
title_full_unstemmed Heterogeneity in surface sensing suggests a division of labor in Pseudomonas aeruginosa populations
title_short Heterogeneity in surface sensing suggests a division of labor in Pseudomonas aeruginosa populations
title_sort heterogeneity in surface sensing suggests a division of labor in pseudomonas aeruginosa populations
topic Microbiology and Infectious Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6615863/
https://www.ncbi.nlm.nih.gov/pubmed/31180327
http://dx.doi.org/10.7554/eLife.45084
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