Revealing the mechanistic basis of reef-building coral tolerance versus susceptibility to low O₂ stress
- Publication Type:
- Thesis
- Issue Date:
- 2022
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Exposure of marine life to low oxygen is accelerating worldwide as a consequence of climate change and localized pollution. Global coral populations have been in significant decline now since the 1950s, experiencing widespread fatal bleaching episodes (i.e., loss of their symbiotic algae). However, only recently have such events been proposed to be directly associated with an inadequate oxygen supply (hypoxia).
I first examined the mechanistic basis for coral hypoxia stress response systems between two common reef-building Acropora species reported to have differential bleaching thresholds to heat stress in the field. As expected, only the less stress-tolerant species bleached under night-time deoxygenated conditions, corresponding to contrasting gene expression profiles indicative of varied effectiveness of their hypoxia-inducible factor (HIF) hypoxia response system (HRS).
I next considered how the responses observed for adult corals applied to coral larvae, where the latter exhibit very different physiologies related to their predominant free-living planktonic (without photosynthetic algae symbionts) versus benthic stages. Despite exhibiting a consistent swimming phenotype compared to control samples, coral planulae demonstrated similar HIF-HRS expression to the adult and differential gene expression that reflected a disruption of pathways involved in developmental regulation, mitochondrial activity, lipid metabolism, and O₂-sensitive epigenetic regulators.
I then incorporated deoxygenated seawater into short-term heat assays and demonstrated that deoxygenation can lower the thermal limit of an Acropora coral species by as much as 0.4 oC and 1oC based on the maximum photosystem II (PSII) photosynthetic efficiency and bleaching index score, respectively. I showed that even heating alone activates putative genes key to the HIF-HRS, which may suggest that a hypoxic state is reached in the coral tissue under heat stress, possibly as a result of an O₂-intensive stress response.
Hypoxia stress associated genes I identified from model Acropora corals were then considered against genomic gene sets of a wider range of coral species based on the notion that a variation in gene copy number can result in differential gene expression with subsequent differences in the effectiveness of any given stress response. Therefore, I used an ortholog-based meta-analysis to investigate how the hypoxia gene set inventory differed amongst 24 coral species. Interestingly, the highest gene copy number was consistently presented by Porites lutea, which is considered to exhibit inherently greater stress tolerance to bleaching. As such, the unevenly expanded (or reduced) hypoxia genes presented here provide key genes of interest to target in examining (or diagnosing) coral stress thresholds.
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