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Differential impact on motility and biofilm dispersal of closely related phosphodiesterases in Pseudomonas aeruginosa
In Pseudomonas aeruginosa, the transition between planktonic and biofilm lifestyles is modulated by the intracellular secondary messenger cyclic dimeric-GMP (c-di-GMP) in response to environmental conditions. Here, we used gene deletions to investigate how the environmental stimulus nitric oxide (NO...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7148300/ https://www.ncbi.nlm.nih.gov/pubmed/32277108 http://dx.doi.org/10.1038/s41598-020-63008-5 |
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author | Cai, Yu-ming Hutchin, Andrew Craddock, Jack Walsh, Martin A. Webb, Jeremy S. Tews, Ivo |
author_facet | Cai, Yu-ming Hutchin, Andrew Craddock, Jack Walsh, Martin A. Webb, Jeremy S. Tews, Ivo |
author_sort | Cai, Yu-ming |
collection | PubMed |
description | In Pseudomonas aeruginosa, the transition between planktonic and biofilm lifestyles is modulated by the intracellular secondary messenger cyclic dimeric-GMP (c-di-GMP) in response to environmental conditions. Here, we used gene deletions to investigate how the environmental stimulus nitric oxide (NO) is linked to biofilm dispersal, focusing on biofilm dispersal phenotype from proteins containing putative c-di-GMP turnover and Per-Arnt-Sim (PAS) sensory domains. We document opposed physiological roles for the genes ΔrbdA and Δpa2072 that encode proteins with identical domain structure: while ΔrbdA showed elevated c-di-GMP levels, restricted motility and promoted biofilm formation, c-di-GMP levels were decreased in Δpa2072, and biofilm formation was inhibited, compared to wild type. A second pair of genes, ΔfimX and ΔdipA, were selected on the basis of predicted impaired c-di-GMP turnover function: ΔfimX showed increased, ΔdipA decreased NO induced biofilm dispersal, and the genes effected different types of motility, with reduced twitching for ΔfimX and reduced swimming for ΔdipA. For all four deletion mutants we find that NO-induced biomass reduction correlates with increased NO-driven swarming, underlining a significant role for this motility in biofilm dispersal. Hence P. aeruginosa is able to differentiate c-di-GMP output using structurally highly related proteins that can contain degenerate c-di-GMP turnover domains. |
format | Online Article Text |
id | pubmed-7148300 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71483002020-04-15 Differential impact on motility and biofilm dispersal of closely related phosphodiesterases in Pseudomonas aeruginosa Cai, Yu-ming Hutchin, Andrew Craddock, Jack Walsh, Martin A. Webb, Jeremy S. Tews, Ivo Sci Rep Article In Pseudomonas aeruginosa, the transition between planktonic and biofilm lifestyles is modulated by the intracellular secondary messenger cyclic dimeric-GMP (c-di-GMP) in response to environmental conditions. Here, we used gene deletions to investigate how the environmental stimulus nitric oxide (NO) is linked to biofilm dispersal, focusing on biofilm dispersal phenotype from proteins containing putative c-di-GMP turnover and Per-Arnt-Sim (PAS) sensory domains. We document opposed physiological roles for the genes ΔrbdA and Δpa2072 that encode proteins with identical domain structure: while ΔrbdA showed elevated c-di-GMP levels, restricted motility and promoted biofilm formation, c-di-GMP levels were decreased in Δpa2072, and biofilm formation was inhibited, compared to wild type. A second pair of genes, ΔfimX and ΔdipA, were selected on the basis of predicted impaired c-di-GMP turnover function: ΔfimX showed increased, ΔdipA decreased NO induced biofilm dispersal, and the genes effected different types of motility, with reduced twitching for ΔfimX and reduced swimming for ΔdipA. For all four deletion mutants we find that NO-induced biomass reduction correlates with increased NO-driven swarming, underlining a significant role for this motility in biofilm dispersal. Hence P. aeruginosa is able to differentiate c-di-GMP output using structurally highly related proteins that can contain degenerate c-di-GMP turnover domains. Nature Publishing Group UK 2020-04-10 /pmc/articles/PMC7148300/ /pubmed/32277108 http://dx.doi.org/10.1038/s41598-020-63008-5 Text en © The Author(s) 2020 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 Cai, Yu-ming Hutchin, Andrew Craddock, Jack Walsh, Martin A. Webb, Jeremy S. Tews, Ivo Differential impact on motility and biofilm dispersal of closely related phosphodiesterases in Pseudomonas aeruginosa |
title | Differential impact on motility and biofilm dispersal of closely related phosphodiesterases in Pseudomonas aeruginosa |
title_full | Differential impact on motility and biofilm dispersal of closely related phosphodiesterases in Pseudomonas aeruginosa |
title_fullStr | Differential impact on motility and biofilm dispersal of closely related phosphodiesterases in Pseudomonas aeruginosa |
title_full_unstemmed | Differential impact on motility and biofilm dispersal of closely related phosphodiesterases in Pseudomonas aeruginosa |
title_short | Differential impact on motility and biofilm dispersal of closely related phosphodiesterases in Pseudomonas aeruginosa |
title_sort | differential impact on motility and biofilm dispersal of closely related phosphodiesterases in pseudomonas aeruginosa |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7148300/ https://www.ncbi.nlm.nih.gov/pubmed/32277108 http://dx.doi.org/10.1038/s41598-020-63008-5 |
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