Transcriptomic changes in coral holobionts provide insights into physiological challenges of future climate and ocean change

• Published in: PLOS ONE
• Main Authors: Kaniewska, Paulina, Chan, Chon-Kit Kenneth, Kline, David, Ling, Edmund Yew Siang, Rosic, Nedeljka, Edwards, David, Hoegh-Guldberg, Ove, Dove, Sophie
• Other Authors: Medina, Mónica
• Format: Article in Journal/Newspaper
• Language: English
• Published: Public Library of Science 2015
• Subjects: Multidisciplinary Sciences; Science & Technology - Other Topics; 1100 Agricultural and Biological Sciences; 1300 Biochemistry; Genetics and Molecular Biology; Ocean acidification
• Online Access: https://espace.library.uq.edu.au/view/UQ:374417

Tropical reef-building coral stress levels will intensify with the predicted rising atmospheric CO2 resulting in ocean temperature and acidification increase. Most studies to date have focused on the destabilization of coral-dinoflagellate symbioses due to warming oceans, or declining calcification due to ocean acidification. In our study, pH and temperature conditions consistent with the end-of-century scenarios of the Intergovernmental Panel on Climate Change (IPCC) caused major changes in photosynthesis and respiration, in addition to decreased calcification rates in the coral Acropora millepora. Population density of symbiotic dinoflagellates (Symbiodinium) under high levels of ocean acidification and temperature (Representative Concentration Pathway, RCP8.5) decreased to half of that found under present day conditions, with photosynthetic and respiratory rates also being reduced by 40%. These physiological changes were accompanied by evidence for gene regulation of calcium and bicarbonate transporters along with components of the organic matrix. Meta-transcriptomic RNA-Seq data analyses showed an overall down regulation of metabolic transcripts, and an increased abundance of transcripts involved in circadian clock control, controlling the damage of oxidative stress, calcium signaling/homeostasis, cytoskeletal interactions, transcription regulation, DNA repair, Wnt signaling and apoptosis/immunity/toxins. We suggest that increased maintenance costs under ocean acidification and warming, and diversion of cellular ATP to pH homeostasis, oxidative stress response, UPR and DNA repair, along with metabolic suppression, may underpin why Acroporid species tend not to thrive under future environmental stress. Our study highlights the potential increased energy demand when the coral holobiont is exposed to high levels of ocean warming and acidification.