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C-di-GMP regulates Pseudomonas aeruginosa stress response to tellurite during both planktonic and biofilm modes of growth

Stress response plays an important role on microbial adaptation under hostile environmental conditions. It is generally unclear how the signaling transduction pathway mediates a stress response in planktonic and biofilm modes of microbial communities simultaneously. Here, we showed that metalloid te...

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Autores principales: Chua, Song Lin, Sivakumar, Krishnakumar, Rybtke, Morten, Yuan, Mingjun, Andersen, Jens Bo, Nielsen, Thomas E., Givskov, Michael, Tolker-Nielsen, Tim, Cao, Bin, Kjelleberg, Staffan, Yang, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438720/
https://www.ncbi.nlm.nih.gov/pubmed/25992876
http://dx.doi.org/10.1038/srep10052
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author Chua, Song Lin
Sivakumar, Krishnakumar
Rybtke, Morten
Yuan, Mingjun
Andersen, Jens Bo
Nielsen, Thomas E.
Givskov, Michael
Tolker-Nielsen, Tim
Cao, Bin
Kjelleberg, Staffan
Yang, Liang
author_facet Chua, Song Lin
Sivakumar, Krishnakumar
Rybtke, Morten
Yuan, Mingjun
Andersen, Jens Bo
Nielsen, Thomas E.
Givskov, Michael
Tolker-Nielsen, Tim
Cao, Bin
Kjelleberg, Staffan
Yang, Liang
author_sort Chua, Song Lin
collection PubMed
description Stress response plays an important role on microbial adaptation under hostile environmental conditions. It is generally unclear how the signaling transduction pathway mediates a stress response in planktonic and biofilm modes of microbial communities simultaneously. Here, we showed that metalloid tellurite (TeO(3)(2–)) exposure induced the intracellular content of the secondary messenger cyclic di-GMP (c-di-GMP) of Pseudomonas aeruginosa. Two diguanylate cyclases (DGCs), SadC and SiaD, were responsible for the increased intracellular content of c-di-GMP. Enhanced c-di-GMP levels by TeO(3)(2–) further increased P. aeruginosa biofilm formation and resistance to TeO(3)(2–). P. aeruginosa ΔsadCΔsiaD and PAO1/p(lac)-yhjH mutants with low intracellular c-di-GMP content were more sensitive to TeO(3)(2–) exposure and had low relative fitness compared to the wild-type PAO1 planktonic and biofilm cultures exposed to TeO(3)(2–). Our study provided evidence that c-di-GMP level can play an important role in mediating stress response in microbial communities during both planktonic and biofilm modes of growth.
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spelling pubmed-44387202015-05-29 C-di-GMP regulates Pseudomonas aeruginosa stress response to tellurite during both planktonic and biofilm modes of growth Chua, Song Lin Sivakumar, Krishnakumar Rybtke, Morten Yuan, Mingjun Andersen, Jens Bo Nielsen, Thomas E. Givskov, Michael Tolker-Nielsen, Tim Cao, Bin Kjelleberg, Staffan Yang, Liang Sci Rep Article Stress response plays an important role on microbial adaptation under hostile environmental conditions. It is generally unclear how the signaling transduction pathway mediates a stress response in planktonic and biofilm modes of microbial communities simultaneously. Here, we showed that metalloid tellurite (TeO(3)(2–)) exposure induced the intracellular content of the secondary messenger cyclic di-GMP (c-di-GMP) of Pseudomonas aeruginosa. Two diguanylate cyclases (DGCs), SadC and SiaD, were responsible for the increased intracellular content of c-di-GMP. Enhanced c-di-GMP levels by TeO(3)(2–) further increased P. aeruginosa biofilm formation and resistance to TeO(3)(2–). P. aeruginosa ΔsadCΔsiaD and PAO1/p(lac)-yhjH mutants with low intracellular c-di-GMP content were more sensitive to TeO(3)(2–) exposure and had low relative fitness compared to the wild-type PAO1 planktonic and biofilm cultures exposed to TeO(3)(2–). Our study provided evidence that c-di-GMP level can play an important role in mediating stress response in microbial communities during both planktonic and biofilm modes of growth. Nature Publishing Group 2015-05-20 /pmc/articles/PMC4438720/ /pubmed/25992876 http://dx.doi.org/10.1038/srep10052 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Chua, Song Lin
Sivakumar, Krishnakumar
Rybtke, Morten
Yuan, Mingjun
Andersen, Jens Bo
Nielsen, Thomas E.
Givskov, Michael
Tolker-Nielsen, Tim
Cao, Bin
Kjelleberg, Staffan
Yang, Liang
C-di-GMP regulates Pseudomonas aeruginosa stress response to tellurite during both planktonic and biofilm modes of growth
title C-di-GMP regulates Pseudomonas aeruginosa stress response to tellurite during both planktonic and biofilm modes of growth
title_full C-di-GMP regulates Pseudomonas aeruginosa stress response to tellurite during both planktonic and biofilm modes of growth
title_fullStr C-di-GMP regulates Pseudomonas aeruginosa stress response to tellurite during both planktonic and biofilm modes of growth
title_full_unstemmed C-di-GMP regulates Pseudomonas aeruginosa stress response to tellurite during both planktonic and biofilm modes of growth
title_short C-di-GMP regulates Pseudomonas aeruginosa stress response to tellurite during both planktonic and biofilm modes of growth
title_sort c-di-gmp regulates pseudomonas aeruginosa stress response to tellurite during both planktonic and biofilm modes of growth
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438720/
https://www.ncbi.nlm.nih.gov/pubmed/25992876
http://dx.doi.org/10.1038/srep10052
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