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11th ICRS Abstract book - Nova Southeastern University

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Oral Mini-Symposium 5: Functional Biology of Corals and Coral Symbiosis: Molecular Biology, Cell Biology and Physiology<br />

5-26<br />

Suicide Is Painless, It Brings On Many Changes: Apoptosis And Autophagy in<br />

Cnidarian-Dinoflagellate Symbiosis.<br />

Simon DUNN* 1 , Sophie DOVE 1<br />

1 Center for Marine Studies, <strong>University</strong> of Queensland, St Lucia, Brisbane, Australia<br />

The underlying cellular pathways that control the onset, maintenance and breakdown of<br />

cnidarian–dinoflagellate symbiosis are just beginning to be described. The pathways that<br />

have been shown to operate during these processes are highly conserved from yeast to<br />

complex metazoans, including higher vertebrates. Two examples of these pathways are<br />

apoptosis and autophagy, which are crucial to development, tissue homeostasis and<br />

immunity. Apoptosis and autophagy leading to the suicide of specific cells has been<br />

shown to be active when the cnidarian-dinoflagellate symbiosis is under stress. Key<br />

molecular components of these signal transduction pathways have been identified in<br />

cnidarians. However, the triggers activating the initiation of these pathways in this<br />

symbiosis remain unresolved and are now under investigation. This study focuses on the<br />

role of mitochondria in these cellular processes.<br />

5-27<br />

Potential Parental Effects On Establishment And Maintenance Of Cnidarian-Algal<br />

Symbioses<br />

Daniel POLAND* 1 , Andrew HANNES 1 , Mary Alice COFFROTH 2<br />

1 Department of Biological Sciences, SUNY at Buffalo, Buffalo, NY, 2 Department of<br />

Geology, SUNY at Buffalo, Buffalo, NY<br />

During early stages of cnidarian-algal symbioses coral recruits acquire a diverse array of<br />

symbiotic dinoflagellate algae (genus Symbiodinium). Yet over time Symbiodinium<br />

diversity within the host is reduced as the adult host-Symbiodinium specificity is<br />

established. The factors controlling this are unclear. Here, we investigated the<br />

establishment of symbioses between a Caribbean octocoral, Briareum asbestinum, and its<br />

Symbiodinium partners. Adult B. asbestinum harbor Symbiodinium of two lineages within<br />

clade B (B178 and B184), which are distinguished by sequence variability in the<br />

chloroplast large subunit (23S) ribosomal DNA. B. asbestinum harbored Symbiodinium<br />

B178 in most Caribbean and Florida Keys populations sampled. However, in the Florida<br />

Keys, a few B. asbestinum populations harbored mostly B184 or B178+B184<br />

Symbiodinium. To investigate the progression of the symbiosis from newly settled polyps<br />

(recruits) to established colonies, asymbiotic larvae were collected from parents with<br />

B184 or B178 Symbiodinium. Larvae from B178 adults were placed in several habitats<br />

and larvae from B184 adults were raised at a site where only B178 adults were found.<br />

Regardless of the Symbiodinium populations in adults, recruits initially harbored<br />

Symbiodinium assemblages dominated by B184, although other algal symbionts were<br />

also present. After 24 months, 98% of recruits originating from parents with B184<br />

Symbiodinium harbored only B184, despite the predominance of B178 in the local host<br />

population. Recruits originating from parents with B178 Symbiodinium showed an<br />

increased frequency of B178 with 10% and 40% of the recruits harboring B178 and<br />

B178+184, respectively, and 50% maintaining only B184 Symbiodinium. These results<br />

suggest that establishment of symbiotic relationships in cnidarians may remain dynamic<br />

for many years following settlement and initial Symbiodinium acquisition.<br />

5-28<br />

Cell-Cycle Regulation in The Dinoflagellate-Cnidarian Symbiosis<br />

Santiago PEREZ* 1 , John PRINGLE 1 , Carlo CARUSO 1<br />

1 Genetics, Stanford, Stanford, CA<br />

Studies of cnidarian-algal symbiosis have described many aspects of their anatomy and<br />

physiology. However, to date, the molecular and cellular underpinnings of these ecologically<br />

important symbioses remain grossly understudied. For example, several studies of the<br />

hydrozoan species Hydra viridis concluded that its symbiotic green-algal cells coordinate<br />

their cell cycles with those of the host cells and that light, inorganic nutrients, and host feeding<br />

are important regulators of this process. Yet, we do not know the mechanisms either of hostsymbiont<br />

coordination or of the environmental influences on the process, nor is it clear whether<br />

the controls that appear to operate in Hydra are also found in other systems such as coraldinoflagellate<br />

symbioses. We are one of several laboratories attempting to develop the small<br />

tropical sea anemone Aiptasia spp. as a tractable laboratory model system for study of the<br />

molecular and cell biology of cnidarian-dinoflagellate symbioses. Aiptasia, like the<br />

scleractinian corals, is symbiotic with dinoflagellates of the genus Symbiodinium, so it is<br />

likely that our results will be widely applicable. We will describe our progress in developing<br />

methods for the study of and in elucidating the coordination between the host and symbiont<br />

cellular reproduction during the initial establishment of the symbiosis, its steady-state<br />

maintenance, and the stress conditions that lead to the breakdown of the symbiois.<br />

5-29<br />

Functional Diversity in The Symbiotic Interactions Between Coral And symbiodinium<br />

Michael STAT* 1 , Emily MORRIS 1 , Ruth GATES 1<br />

1 HIMB, <strong>University</strong> of Hawaii, Kaneohe, HI<br />

The symbiotic continuum ranges between mutualism and parasitism. In coral-dinoflagellate<br />

symbiosis, the interaction has been defined as mutualistic via the exchange of organic and<br />

inorganic nutrients that in turn allows for the growth and formation of coral reefs. The<br />

symbiotic dinoflagellate genus Symbiodinium is genetically diverse containing eight broad<br />

lineages (clades A-H). Corals predominantly associate with clade C Symbiodinium, and less<br />

commonly with clades A, B, D, F, and G. Variation in the function and interactive physiology<br />

of different coral-dinoflagellate assemblages is virtually unexplored but important to our<br />

understanding of factors that contribute to coral reef resilience. In this study, we evaluated the<br />

symbiotic interaction between coral and Symbiodinium belonging to two clades, A and C. We<br />

approached this using ecological, phylogenetic, and biochemical analyses. Our data shows 1)<br />

that there is a significant correlation between the presence of Symbiodinium clade A and<br />

health compromised corals; 2) that phylogenetic and genetic distance analyses place clade A as<br />

more closely related to free-living dinoflagellates than the other Symbiodinium lineages; and<br />

3) that Symbiodinium clade A fixes and releases significantly lower amounts of carbon in the<br />

presence of a coral synthetic host factor than clade C. Collectively these data demonstrate that<br />

the interaction between coral and Symbiodinium clade A is not the same as the relationship<br />

between clade C and coral and that along the symbiotic continuum the interaction between<br />

clade A and coral is closer to parasitic than mutualistic in nature.<br />

32

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