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Salt Shock Responses of Microcystis Revealed through Physiological, Transcript, and Metabolomic Analyses

The transfer of Microcystis aeruginosa from freshwater to estuaries has been described worldwide and salinity is reported as the main factor controlling the expansion of M. aeruginosa to coastal environments. Analyzing the expression levels of targeted genes and employing both targeted and non-targe...

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Autores principales: Georges des Aulnois, Maxime, Réveillon, Damien, Robert, Elise, Caruana, Amandine, Briand, Enora, Guljamow, Arthur, Dittmann, Elke, Amzil, Zouher, Bormans, Myriam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7150857/
https://www.ncbi.nlm.nih.gov/pubmed/32197406
http://dx.doi.org/10.3390/toxins12030192
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author Georges des Aulnois, Maxime
Réveillon, Damien
Robert, Elise
Caruana, Amandine
Briand, Enora
Guljamow, Arthur
Dittmann, Elke
Amzil, Zouher
Bormans, Myriam
author_facet Georges des Aulnois, Maxime
Réveillon, Damien
Robert, Elise
Caruana, Amandine
Briand, Enora
Guljamow, Arthur
Dittmann, Elke
Amzil, Zouher
Bormans, Myriam
author_sort Georges des Aulnois, Maxime
collection PubMed
description The transfer of Microcystis aeruginosa from freshwater to estuaries has been described worldwide and salinity is reported as the main factor controlling the expansion of M. aeruginosa to coastal environments. Analyzing the expression levels of targeted genes and employing both targeted and non-targeted metabolomic approaches, this study investigated the effect of a sudden salt increase on the physiological and metabolic responses of two toxic M. aeruginosa strains separately isolated from fresh and brackish waters, respectively, PCC 7820 and 7806. Supported by differences in gene expressions and metabolic profiles, salt tolerance was found to be strain specific. An increase in salinity decreased the growth of M. aeruginosa with a lesser impact on the brackish strain. The production of intracellular microcystin variants in response to salt stress correlated well to the growth rate for both strains. Furthermore, the release of microcystins into the surrounding medium only occurred at the highest salinity treatment when cell lysis occurred. This study suggests that the physiological responses of M. aeruginosa involve the accumulation of common metabolites but that the intraspecific salt tolerance is based on the accumulation of specific metabolites. While one of these was determined to be sucrose, many others remain to be identified. Taken together, these results provide evidence that M. aeruginosa is relatively salt tolerant in the mesohaline zone and microcystin (MC) release only occurs when the capacity of the cells to deal with salt increase is exceeded.
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spelling pubmed-71508572020-04-20 Salt Shock Responses of Microcystis Revealed through Physiological, Transcript, and Metabolomic Analyses Georges des Aulnois, Maxime Réveillon, Damien Robert, Elise Caruana, Amandine Briand, Enora Guljamow, Arthur Dittmann, Elke Amzil, Zouher Bormans, Myriam Toxins (Basel) Article The transfer of Microcystis aeruginosa from freshwater to estuaries has been described worldwide and salinity is reported as the main factor controlling the expansion of M. aeruginosa to coastal environments. Analyzing the expression levels of targeted genes and employing both targeted and non-targeted metabolomic approaches, this study investigated the effect of a sudden salt increase on the physiological and metabolic responses of two toxic M. aeruginosa strains separately isolated from fresh and brackish waters, respectively, PCC 7820 and 7806. Supported by differences in gene expressions and metabolic profiles, salt tolerance was found to be strain specific. An increase in salinity decreased the growth of M. aeruginosa with a lesser impact on the brackish strain. The production of intracellular microcystin variants in response to salt stress correlated well to the growth rate for both strains. Furthermore, the release of microcystins into the surrounding medium only occurred at the highest salinity treatment when cell lysis occurred. This study suggests that the physiological responses of M. aeruginosa involve the accumulation of common metabolites but that the intraspecific salt tolerance is based on the accumulation of specific metabolites. While one of these was determined to be sucrose, many others remain to be identified. Taken together, these results provide evidence that M. aeruginosa is relatively salt tolerant in the mesohaline zone and microcystin (MC) release only occurs when the capacity of the cells to deal with salt increase is exceeded. MDPI 2020-03-18 /pmc/articles/PMC7150857/ /pubmed/32197406 http://dx.doi.org/10.3390/toxins12030192 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Georges des Aulnois, Maxime
Réveillon, Damien
Robert, Elise
Caruana, Amandine
Briand, Enora
Guljamow, Arthur
Dittmann, Elke
Amzil, Zouher
Bormans, Myriam
Salt Shock Responses of Microcystis Revealed through Physiological, Transcript, and Metabolomic Analyses
title Salt Shock Responses of Microcystis Revealed through Physiological, Transcript, and Metabolomic Analyses
title_full Salt Shock Responses of Microcystis Revealed through Physiological, Transcript, and Metabolomic Analyses
title_fullStr Salt Shock Responses of Microcystis Revealed through Physiological, Transcript, and Metabolomic Analyses
title_full_unstemmed Salt Shock Responses of Microcystis Revealed through Physiological, Transcript, and Metabolomic Analyses
title_short Salt Shock Responses of Microcystis Revealed through Physiological, Transcript, and Metabolomic Analyses
title_sort salt shock responses of microcystis revealed through physiological, transcript, and metabolomic analyses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7150857/
https://www.ncbi.nlm.nih.gov/pubmed/32197406
http://dx.doi.org/10.3390/toxins12030192
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