Antibiotics Alter Pocillopora Coral-Symbiodiniaceae-Bacteria Interactions and Cause Microbial Dysbiosis During Heat Stress

Journal article


Connelly, M.T., McRae, C.J., Liu, P.J., Martin, C. and Traylor-Knowles, N. (2022). Antibiotics Alter Pocillopora Coral-Symbiodiniaceae-Bacteria Interactions and Cause Microbial Dysbiosis During Heat Stress. Frontiers in Marine Science. 8. https://doi.org/10.3389/fmars.2021.814124
AuthorsConnelly, M.T., McRae, C.J., Liu, P.J., Martin, C. and Traylor-Knowles, N.
Abstract

Symbioses between eukaryotes and their associated microbial communities are fundamental processes that affect organisms’ ecology and evolution. A unique example of this is reef-building corals that maintain symbiotic associations with dinoflagellate algae (Symbiodiniaceae) and bacteria that affect coral health through various mechanisms. However, little is understood about how coral-associated bacteria communities affect holobiont heat tolerance. In this study, we investigated these interactions in four Pocillopora coral colonies belonging to three cryptic species by subjecting fragments to treatments with antibiotics intended to suppress the normal bacteria community, followed by acute heat stress. Separate treatments with only antibiotics or heat stress were conducted to compare the effects of individual stressors on holobiont transcriptome responses and microbiome shifts. Across all Pocillopora species examined, combined antibiotics and heat stress treatment significantly altered coral-associated bacteria communities and caused major changes in both coral and Cladocopium algal symbiont gene expression. Individually, heat stress impaired Pocillopora protein translation and activated DNA repair processes, while antibiotics treatments caused downregulation of Pocillopora amino acid and inorganic ion transport and metabolism genes and Cladocopium photosynthesis genes. Combined antibiotics-heat stress treatments caused synergistic effects on Pocillopora and Cladocopium gene expression including enhanced expression of oxidative stress response genes, programed cell death pathways and proteolytic enzymes that indicate an exacerbated response to heat stress following bacteria community suppression. Collectively, these results provide further evidence that corals and their Symbiodiniaceae and bacteria communities engage in highly coordinated metabolic interactions that are crucial for coral holobiont health, homeostasis, and heat tolerance.

Keywordscoral, holobiont, transcriptome, microbiome, antibiotics, bacteria, dysbiosis
Year2022
JournalFrontiers in Marine Science
Journal citation8
PublisherFrontiers Media
ISSN2296-7745
Digital Object Identifier (DOI)https://doi.org/10.3389/fmars.2021.814124
Web address (URL)https://www.frontiersin.org/articles/10.3389/fmars.2021.814124/full
Publication dates
Print13 Jan 2022
Publication process dates
Accepted22 Dec 2021
Deposited02 May 2024
Publisher's version
License
File Access Level
Open
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Gene Expression Response to Stony Coral Tissue Loss Disease Transmission in M. cavernosa and O. faveolata From Florida
Traylor-Knowles, N., Connelly, M. T., Young, B. D., Eaton, K., Muller, E. M., Paul, V. J., Ushijima, B., DeMerlis, A., Drown, M. K., Goncalves, A., Kron, N., Snyder, G. A., Martin, C. and Rodriguez, K. (2021). Gene Expression Response to Stony Coral Tissue Loss Disease Transmission in M. cavernosa and O. faveolata From Florida. Frontiers in Marine Science. 8 (681563). https://doi.org/10.3389/fmars.2021.681563