Proteomics Links the Redox State to Calcium Signaling During Bleaching of the Scleractinian Coral Acropora microphthalma on Exposure to High Solar Irradiance and Thermal Stress[S]

• Published in: Molecular & cellular proteomics Vol. 14; no. 3; pp. 585 - 595
• Main Authors: Weston, Andrew J., Dunlap, Walter C., Beltran, Victor H., Starcevic, Antonio, Hranueli, Daslav, Ward, Malcolm, Long, Paul F.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.03.2015; The American Society for Biochemistry and Molecular Biology
• Subjects: Acropora microphthalma; Algal Proteins - analysis; Animals; Anthozoa - physiology; Anthozoa - radiation effects; Calcium Signaling; Cyanobacteria - physiology; Gene Expression Regulation; Oxidation-Reduction; Photosynthesis; Proteomics - methods; Scleractinia; Skin Lightening Preparations; Stress, Physiological; Sunlight; Symbiodinium; Symbiosis; Temperature
• DOI: 10.1074/mcp.M114.043125
• ISSN: 1535-9476; 1535-9484

Shipboard experiments were each performed over a 2 day period to examine the proteomic response of the symbiotic coral Acropora microphthalma exposed to acute conditions of high temperature/low light or high light/low temperature stress. During these treatments, corals had noticeably bleached. The photosynthetic performance of residual algal endosymbionts was severely impaired but showed signs of recovery in both treatments by the end of the second day. Changes in the coral proteome were determined daily and, using recently available annotated genome sequences, the individual contributions of the coral host and algal endosymbionts could be extracted from these data. Quantitative changes in proteins relevant to redox state and calcium metabolism are presented. Notably, expression of common antioxidant proteins was not detected from the coral host but present in the algal endosymbiont proteome. Possible roles for elevated carbonic anhydrase in the coral host are considered: to restore intracellular pH diminished by loss of photosynthetic activity, to indirectly limit intracellular calcium influx linked with enhanced calmodulin expression to impede late-stage symbiont exocytosis, or to enhance inorganic carbon transport to improve the photosynthetic performance of algal symbionts that remain in hospite. Protein effectors of calcium-dependent exocytosis were present in both symbiotic partners. No caspase-family proteins associated with host cell apoptosis, with exception of the autophagy chaperone HSP70, were detected, suggesting that algal loss and photosynthetic dysfunction under these experimental conditions were not due to host-mediated phytosymbiont destruction. Instead, bleaching occurred by symbiont exocytosis and loss of light-harvesting pigments of algae that remain in hospite. These proteomic data are, therefore, consistent with our premise that coral endosymbionts can mediate their own retention or departure from the coral host, which may manifest as “symbiont shuffling” of Symbiodinium clades in response to environmental stress.