Diagnostic gene expression biomarkers of coral thermal stress.

Gene expression biomarkers can enable rapid assessment of physiological conditions in situ, providing a valuable tool for reef managers interested in linking organism physiology with large-scale climatic conditions. Here, we assessed the ability of quantitative PCR (qPCR)-based gene expression biomarkers to evaluate (i) the immediate cellular stress response (CSR) of Porites astreoides to incremental thermal stress and (ii) the magnitude of CSR and cellular homeostasis response (CHR) during a natural bleaching event. Expression levels largely scaled with treatment temperature, with the strongest responses occurring in heat-shock proteins. This is the first demonstration of a 'tiered' CSR in a coral, where the magnitude of expression change is proportional to stress intensity. Analysis of a natural bleaching event revealed no signature of an acute CSR in normal or bleached corals, indicating that the bleaching stressor(s) had abated by the day of sampling. Another long-term stress CHR-based indicator assay was significantly elevated in bleached corals, although assay values overall were low, suggesting good prospects for recovery. This study represents the first step in linking variation in gene expression biomarkers to stress tolerance and bleaching thresholds in situ by quantifying the severity of ongoing thermal stress and its accumulated long-term impacts.

Differential effects of copper on three species of scleractinian corals and their algal symbionts (Symbiodinium spp.).

Land-based sources of pollution have been identified as significant stressors linked to the widespread declines of coral cover in coastal reef ecosystems over the last 30 years. Metal contaminants, although noted as a concern, have not been closely monitored in these sensitive ecosystems, nor have their potential impacts on coral-algal symbioses been characterized. In this study, three species of laboratory-reared scleractinian corals, Acropora cervicornis, Pocillopora damicornis, and Montastraea faveolata each containing different algal symbionts (Symbiodinium A3, C1 and D1a, respectively) were exposed to copper (ranging from 2 to 20microg/L) for 5 weeks. At the end of the exposure period, copper had accumulated in the endosymbiotic dinoflagellate ("zooxanthellae") and animal tissue of A. cervicornis and the animal tissue of M. faveolata; however, no copper accumulation was detected in the zooxanthellae or animal tissue of P. damicornis. The three coral species exhibited significantly different sensitivities to copper, with effects occurring in A. cervicornis and P. damicornis at copper concentrations as low as 4microg/L. Copper exposure affected zooxanthellae photosynthesis in A. cervicornis and P. damicornis, and carbonic anhydrase was significantly decreased in A. cervicornis and M. faveolata. Likewise, significant decreases in skeletal growth were observed in A. cervicornis and P. damicornis after copper exposure. Based on preliminary results, no changes in Symbiodinium communities were apparent in response to increasing copper concentration. These results indicate that the relationships between physiological/toxicological endpoints and copper accumulation between coral species differ, suggesting different mechanisms of toxicity and/or susceptibility. This may be driven, in part, by differences in the algal symbiont communities of the coral species in question.

Differential susceptibility to oxidative stress of two scleractinian corals: antioxidant functioning of mycosporine-glycine.

This study examined the importance of mycosporine-glycine (Myc-Gly) as a functional antioxidant in the thermal-stress susceptibility of two scleractinian corals, Platygyra ryukyuensis and Stylophora pistillata. Photochemical efficiency of PSII (F(v)/F(m)), activity of antioxidant enzymes, superoxide dismutase (SOD) and catalase (CAT), and composition and abundance of mycosporine-like amino acids (MAAs) in the coral tissue and in symbiotic zooxanthellae were analyzed during 12-h exposure to high temperature (33 degrees C). After 6- and 12-h exposures at 33 degrees C, S. pistillata showed a significantly more pronounced decline in F(v)/F(m) compared to P. ryukyuensis. A 6-h exposure at 33 degrees C induced a significant increase in the activities of SOD and CAT in both host and zooxanthellae components of S. pistillata while in P. ryukyuensis a significant increase was observed only in the CAT activity of zooxanthellae. After 12-h exposure, the SOD activity of P. ryukyuensis was unaffected in the coral tissue but slightly increased in zooxanthellae, whereas the CAT activity in the coral tissue showed a 2.5-fold increase. The total activity of antioxidant enzymes was significantly higher in S. pistillata than in P. ryukyuensis, suggesting that P. ryukyuensis is less sensitive to oxidative stress than S. pistillata. This differential susceptibility of the corals is consistent with a 20-fold higher initial concentration of Myc-Gly in P. ryukyuensis compared to S. pistillata. In the coral tissue and zooxanthellae of both species investigated, the first 6 h of exposure to thermal stress induced a pronounced reduction in the abundance of Myc-Gly but not in other MAAs. When exposure was prolonged to 12 h, the Myc-Gly pool continued to decrease in P. ryukyuensis and was completely depleted in S. pistillata. The delay in the onset of oxidative stress in P. ryukyuensis and the dramatic increase in the activities of the antioxidant enzymes in S. pistillata, which contains low concentrations of Myc-Gly suggest that Myc-Gly provides rapid protection against oxidative stress before the antioxidant enzymes are induced. These findings strongly suggest that Myc-Gly is functioning as a biological antioxidant in the coral tissue and zooxanthellae and demonstrate its importance in the survival of reef-building corals under thermal stress.