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A stable symbiosis between corals and dinoflagellate algae is crucial for coral reef health, and it is driven by nutrient exchange and environmental interactions. Our understanding of the homeostasis between host cnidarian and algal symbiont during the host adult stage is a longtime area of focus, but little is known about the balance of partners during development and regeneration. We investigated the role of symbiotic algae and heterotrophic feeding on development in the sea anemone model organism commonly called Aiptasia. We focused on asexually-produced offspring (G1), examining the effects of autotrophic and heterotrophic nutrition on developmental rates. We found that the presence of symbionts enhanced growth in fed conditions but impeded development and survival under starvation. The effect of symbiont presence on starved offspring was dose-dependent where those offspring with more symbionts at an earlier stage lost tentacles and mass faster than those with fewer symbionts. We hypothesize that suppression of immunity during development explains the patterns we observe. Our results provide insight into the metabolic costs and benefits of symbiosis under different nutritional conditions during development and regeneration of symbiotic cnidarians.
A stable symbiosis between corals and dinoflagellate algae is crucial for coral reef health, and it is driven by nutrient exchange and environmental interactions. Our understanding of the homeostasis between host cnidarian and algal symbiont during the host adult stage is a longtime area of focus, but little is known about the balance of partners during development and regeneration. We investigated the role of symbiotic algae and heterotrophic feeding on development in the sea anemone model organism commonly called Aiptasia. We focused on asexually-produced offspring (G1), examining the effects of autotrophic and heterotrophic nutrition on developmental rates. We found that the presence of symbionts enhanced growth in fed conditions but impeded development and survival under starvation. The effect of symbiont presence on starved offspring was dose-dependent where those offspring with more symbionts at an earlier stage lost tentacles and mass faster than those with fewer symbionts. We hypothesize that suppression of immunity during development explains the patterns we observe. Our results provide insight into the metabolic costs and benefits of symbiosis under different nutritional conditions during development and regeneration of symbiotic cnidarians.
Reef-building corals depend on symbiosis with photosynthetic algae that reside within their cells. As important as this relationship is for maintaining healthy reefs, it is strikingly delicate. When ocean temperatures briefly exceed the average summer maximum, corals can bleach, losing their endosymbionts. Although the mechanisms governing bleaching are unknown, studies implicate uncoupling of coral and algal cell divisions at high temperatures. Still, little is known regarding the coordination of host and algal cell divisions. Control of nutrient exchange is one likely mechanism. Both nitrogen and phosphate are necessary for dividing cells, and although nitrogen enrichment is known to increase symbiont density in the host, the consequences of phosphate enrichment are poorly understood. Here, we examined the effects of phosphate depletion on symbiont growth in culture and compared the physiology of phosphate-starved symbionts in culture to symbionts that were freshly isolated from a host. We found that available phosphate is as low in freshly isolated symbionts as it is in phosphate-starved cultures. Furthermore, RNAseq revealed that phosphate-limited and freshly isolated symbionts have similar patterns of gene expression for phosphate-dependent genes, most notably upregulation of phosphatases, which is consistent with phosphate recycling. Similarly, lipid profiling revealed a substantial decrease in phospholipid abundance in both phosphate-starved cultures and freshly isolated symbionts. These findings are important because they suggest that limited access to phosphate controls algal cell divisions within a host. IMPORTANCE The corals responsible for building tropical reefs are disappearing at an alarming rate as elevated sea temperatures cause them to bleach and lose the algal symbionts they rely on. Without these symbionts, corals are unable to harvest energy from sunlight and, therefore, struggle to thrive or even survive in the nutrient-poor waters of the tropics. To devise solutions to address the threat to coral reefs, it is necessary to understand the cellular events underpinning the bleaching process. One model for bleaching proposes that heat stress impairs algal photosynthesis and transfer of sugar to the host. Consequently, the host’s demands for nitrogen decrease, increasing nitrogen availability to the symbionts, which leads to an increase in algal proliferation that overwhelms the host. Our work suggests that phosphate may play a similar role to nitrogen in this feedback loop.
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