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Carbon starvation of Pseudomonas aeruginosa biofilms selects for dispersal insensitive mutants

BACKGROUND: Biofilms disperse in response to specific environmental cues, such as reduced oxygen concentration, changes in nutrient concentration and exposure to nitric oxide. Interestingly, biofilms do not completely disperse under these conditions, which is generally attributed to physiological he...

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Autores principales: Nair, Harikrishnan A. S., Subramoni, Sujatha, Poh, Wee Han, Hasnuddin, Nabilah Taqiah Binte, Tay, Martin, Givskov, Michael, Tolker-Nielsen, Tim, Kjelleberg, Staffan, McDougald, Diane, Rice, Scott A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459498/
https://www.ncbi.nlm.nih.gov/pubmed/34551714
http://dx.doi.org/10.1186/s12866-021-02318-8
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author Nair, Harikrishnan A. S.
Subramoni, Sujatha
Poh, Wee Han
Hasnuddin, Nabilah Taqiah Binte
Tay, Martin
Givskov, Michael
Tolker-Nielsen, Tim
Kjelleberg, Staffan
McDougald, Diane
Rice, Scott A.
author_facet Nair, Harikrishnan A. S.
Subramoni, Sujatha
Poh, Wee Han
Hasnuddin, Nabilah Taqiah Binte
Tay, Martin
Givskov, Michael
Tolker-Nielsen, Tim
Kjelleberg, Staffan
McDougald, Diane
Rice, Scott A.
author_sort Nair, Harikrishnan A. S.
collection PubMed
description BACKGROUND: Biofilms disperse in response to specific environmental cues, such as reduced oxygen concentration, changes in nutrient concentration and exposure to nitric oxide. Interestingly, biofilms do not completely disperse under these conditions, which is generally attributed to physiological heterogeneity of the biofilm. However, our results suggest that genetic heterogeneity also plays an important role in the non-dispersing population of P. aeruginosa in biofilms after nutrient starvation. RESULTS: In this study, 12.2% of the biofilm failed to disperse after 4 d of continuous starvation-induced dispersal. Cells were recovered from the dispersal phase as well as the remaining biofilm. For 96 h starved biofilms, rugose small colony variants (RSCV) were found to be present in the biofilm, but were not observed in the dispersal effluent. In contrast, wild type and small colony variants (SCV) were found in high numbers in the dispersal phase. Genome sequencing of these variants showed that most had single nucleotide mutations in genes associated with biofilm formation, e.g. in wspF, pilT, fha1 and aguR. Complementation of those mutations restored starvation-induced dispersal from the biofilms. Because c-di-GMP is linked to biofilm formation and dispersal, we introduced a c-di-GMP reporter into the wild-type P. aeruginosa and monitored green fluorescent protein (GFP) expression before and after starvation-induced dispersal. Post dispersal, the microcolonies were smaller and significantly brighter in GFP intensity, suggesting the relative concentration of c-di-GMP per cell within the microcolonies was also increased. Furthermore, only the RSCV showed increased c-di-GMP, while wild type and SCV were no different from the parental strain. CONCLUSIONS: This suggests that while starvation can induce dispersal from the biofilm, it also results in strong selection for mutants that overproduce c-di-GMP and that fail to disperse in response to the dispersal cue, starvation.
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spelling pubmed-84594982021-09-23 Carbon starvation of Pseudomonas aeruginosa biofilms selects for dispersal insensitive mutants Nair, Harikrishnan A. S. Subramoni, Sujatha Poh, Wee Han Hasnuddin, Nabilah Taqiah Binte Tay, Martin Givskov, Michael Tolker-Nielsen, Tim Kjelleberg, Staffan McDougald, Diane Rice, Scott A. BMC Microbiol Research BACKGROUND: Biofilms disperse in response to specific environmental cues, such as reduced oxygen concentration, changes in nutrient concentration and exposure to nitric oxide. Interestingly, biofilms do not completely disperse under these conditions, which is generally attributed to physiological heterogeneity of the biofilm. However, our results suggest that genetic heterogeneity also plays an important role in the non-dispersing population of P. aeruginosa in biofilms after nutrient starvation. RESULTS: In this study, 12.2% of the biofilm failed to disperse after 4 d of continuous starvation-induced dispersal. Cells were recovered from the dispersal phase as well as the remaining biofilm. For 96 h starved biofilms, rugose small colony variants (RSCV) were found to be present in the biofilm, but were not observed in the dispersal effluent. In contrast, wild type and small colony variants (SCV) were found in high numbers in the dispersal phase. Genome sequencing of these variants showed that most had single nucleotide mutations in genes associated with biofilm formation, e.g. in wspF, pilT, fha1 and aguR. Complementation of those mutations restored starvation-induced dispersal from the biofilms. Because c-di-GMP is linked to biofilm formation and dispersal, we introduced a c-di-GMP reporter into the wild-type P. aeruginosa and monitored green fluorescent protein (GFP) expression before and after starvation-induced dispersal. Post dispersal, the microcolonies were smaller and significantly brighter in GFP intensity, suggesting the relative concentration of c-di-GMP per cell within the microcolonies was also increased. Furthermore, only the RSCV showed increased c-di-GMP, while wild type and SCV were no different from the parental strain. CONCLUSIONS: This suggests that while starvation can induce dispersal from the biofilm, it also results in strong selection for mutants that overproduce c-di-GMP and that fail to disperse in response to the dispersal cue, starvation. BioMed Central 2021-09-22 /pmc/articles/PMC8459498/ /pubmed/34551714 http://dx.doi.org/10.1186/s12866-021-02318-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Nair, Harikrishnan A. S.
Subramoni, Sujatha
Poh, Wee Han
Hasnuddin, Nabilah Taqiah Binte
Tay, Martin
Givskov, Michael
Tolker-Nielsen, Tim
Kjelleberg, Staffan
McDougald, Diane
Rice, Scott A.
Carbon starvation of Pseudomonas aeruginosa biofilms selects for dispersal insensitive mutants
title Carbon starvation of Pseudomonas aeruginosa biofilms selects for dispersal insensitive mutants
title_full Carbon starvation of Pseudomonas aeruginosa biofilms selects for dispersal insensitive mutants
title_fullStr Carbon starvation of Pseudomonas aeruginosa biofilms selects for dispersal insensitive mutants
title_full_unstemmed Carbon starvation of Pseudomonas aeruginosa biofilms selects for dispersal insensitive mutants
title_short Carbon starvation of Pseudomonas aeruginosa biofilms selects for dispersal insensitive mutants
title_sort carbon starvation of pseudomonas aeruginosa biofilms selects for dispersal insensitive mutants
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459498/
https://www.ncbi.nlm.nih.gov/pubmed/34551714
http://dx.doi.org/10.1186/s12866-021-02318-8
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