Epstein, Hannah E and Brown, Tanya and Akinrinade, Ayọmikun O and McMinds, Ryan and Pollock, F Joseph and Sonett, Dylan and Smith, Styles and Bourne, David G and Carpenter, Carolina S and Knight, Rob and Willis, Bette L and Medina, Mónica and Lamb, Joleah B and Thurber, Rebecca Vega and Zaneveld, Jesse R (2025) Evidence for microbially-mediated tradeoffs between growth and defense throughout coral evolution. Animal Microbiome, 7 (1). p. 1. DOI https://doi.org/10.1186/s42523-024-00370-z
Epstein, Hannah E and Brown, Tanya and Akinrinade, Ayọmikun O and McMinds, Ryan and Pollock, F Joseph and Sonett, Dylan and Smith, Styles and Bourne, David G and Carpenter, Carolina S and Knight, Rob and Willis, Bette L and Medina, Mónica and Lamb, Joleah B and Thurber, Rebecca Vega and Zaneveld, Jesse R (2025) Evidence for microbially-mediated tradeoffs between growth and defense throughout coral evolution. Animal Microbiome, 7 (1). p. 1. DOI https://doi.org/10.1186/s42523-024-00370-z
Epstein, Hannah E and Brown, Tanya and Akinrinade, Ayọmikun O and McMinds, Ryan and Pollock, F Joseph and Sonett, Dylan and Smith, Styles and Bourne, David G and Carpenter, Carolina S and Knight, Rob and Willis, Bette L and Medina, Mónica and Lamb, Joleah B and Thurber, Rebecca Vega and Zaneveld, Jesse R (2025) Evidence for microbially-mediated tradeoffs between growth and defense throughout coral evolution. Animal Microbiome, 7 (1). p. 1. DOI https://doi.org/10.1186/s42523-024-00370-z
Abstract
Background Evolutionary tradeoffs between life-history strategies are important in animal evolution. Because microbes can influence multiple aspects of host physiology, including growth rate and susceptibility to disease or stress, changes in animal-microbial symbioses have the potential to mediate life-history tradeoffs. Scleractinian corals provide a biodiverse, data-rich, and ecologically-relevant host system to explore this idea. Results Using a comparative approach, we tested if coral microbiomes correlate with disease susceptibility across 425 million years of coral evolution by conducting a cross-species coral microbiome survey (the "Global Coral Microbiome Project") and combining the results with long-term global disease prevalence and coral trait data. Interpreting these data in their phylogenetic context, we show that microbial dominance predicts disease susceptibility, and traced this dominance-disease association to a single putatively beneficial symbiont genus, Endozoicomonas. Endozoicomonas relative abundance in coral tissue explained 30% of variation in disease susceptibility and 60% of variation in microbiome dominance across 40 coral genera, while also correlating strongly with high growth rates. Conclusions These results demonstrate that the evolution of Endozoicomonas symbiosis in corals correlates with both disease prevalence and growth rate, and suggest a mediating role. Exploration of the mechanistic basis for these findings will be important for our understanding of how microbial symbioses influence animal life-history tradeoffs.
Item Type: | Article |
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Uncontrolled Keywords: | Evolutionary tradeoffs; Evolution; Coral disease; Coral microbiome; Coral reefs |
Subjects: | Z Bibliography. Library Science. Information Resources > ZZ OA Fund (articles) |
Divisions: | Faculty of Science and Health Faculty of Science and Health > Life Sciences, School of |
SWORD Depositor: | Unnamed user with email elements@essex.ac.uk |
Depositing User: | Unnamed user with email elements@essex.ac.uk |
Date Deposited: | 13 Jan 2025 13:42 |
Last Modified: | 13 Jan 2025 13:43 |
URI: | http://repository.essex.ac.uk/id/eprint/40017 |
Available files
Filename: s42523-024-00370-z.pdf
Licence: Creative Commons: Attribution 4.0