4.7 Article

Evaluating bivalve cytoprotective responses and their regulatory pathways in a climate change scenario

Journal

SCIENCE OF THE TOTAL ENVIRONMENT
Volume 720, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.scitotenv.2020.137733

Keywords

Temperature; Antibiotic; Metal; Stress response; Transcriptional control; Marine mussel

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Temperature is a relevant abiotic factor affecting physiological performance and distribution of marine animals in natural environments. The changes in global seawater temperatures make it necessary to understand how molecular mechanisms operate under the cumulative effects of global climate change and chemical pollution to promote/hamper environmental acclimatization. Marine mussels are excellent model organisms to infer the impacts of those anthropogenic threats on coastal ecosystems. In this study, Mediterranean mussels (Mytilus galloprovincialis) were exposed to different concentrations of the metal copper (Cu as CuCl2: 2.5, 5, 10, 20, 40 mu g/L) or the antibiotic oxytetracycline (OTC: 0.1, 1, 10, 100, 1000 mu g/L) at increasing seawater temperatures (16 degrees C, 20 degrees C, 24 degrees C). Transcriptional modulation of a 70-kDa heat shock protein (HSP70) and of the ABC transporter P-glycoprotein (P-gp, encoded by the ABCB gene) was assessed along with the cAMP/PKA signaling pathway regulating both gene expressions. At the physiological temperature of mussels (16 degrees C), Cu and OTC induced bimodal changes of cAMP levels and PKA activities in gills of exposed animals. A correlation between OTC- or Cu-induced changes of PKA activity and expression of hsp70 and ABCB was observed. Temperature increases (up to 24 degrees C) altered ABCB and hsp70 responses to the pollutants and disrupted their relationship with cAMP/PKA modulation, leading to loss of correlation between the biological endpoints. On the whole, the results indicate that temperature may impair the effects of inorganic and organic chemicals on the cAMP/PKA signaling pathway of mussels, in turn altering key molecular mediators of physiological plasticity and cytoprotection. (C) 2020 Elsevier B.V. All rights reserved.

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