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

Abstract : The transfer of from freshwater to estuaries has been described worldwide and salinity is reported as the main factor controlling the expansion of 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 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 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 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 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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Contributor : Myriam Bormans Connect in order to contact the contributor
Submitted on : Friday, November 13, 2020 - 3:51:18 PM
Last modification on : Wednesday, November 3, 2021 - 5:34:59 AM
Long-term archiving on: : Sunday, February 14, 2021 - 8:17:17 PM


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Maxime Georges Des Aulnois, Damien Réveillon, Elise Robert, Amandine Caruana, Enora Briand, et al.. Salt Shock Responses of Microcystis Revealed through Physiological, Transcript, and Metabolomic Analyses. Toxins, MDPI, 2020, 12 (3), pp.192. ⟨10.3390/toxins12030192⟩. ⟨hal-03004335⟩



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