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Biology subjects

Gorman, L. M.

Publications and source records attributed to Gorman, L. M..

2 recordsLinked to original sources

Contrasting defensive strategies underlie differential susceptibility of corals to crown-of-thorns sea star (CoTS; Acanthaster cf. solaris) predation

Crown-of-thorns sea star (CoTS), Acanthaster cf. solaris, outbreaks are a major cause of hard coral cover decline across the west Pacific, threatening coral reefs. Coral taxa vary in susceptibility to CoTS predation from preferred (Acropora spp.) to non-preferred (Porites spp.), yet the mechanisms underlying these differences are poorly understood. We investigated coral defenses during an ongoing CoTS outbreak in Moorea, French Polynesia by examining gene expression (including putative toxin genes) in healthy and actively predated colonies of a preferred (Acropora hyacinthus) and a non-preferred (Porites sp.) coral prey species. During predation, A. hyacinthus exhibited molecular signatures of cellular stress responses involving oxidative stress signalling, inflammation, and tissue proteolysis. In contrast, Porites sp. showed enrichment of genes involved in mitochondrial metabolic adjustment and aerobic metabolism, suggesting metabolic compensation to maintain cellular function. Furthermore, A. hyacinthus demonstrated a reactive defense behaviour by differentially expressing toxins (e.g., kunitz-type neurotoxins) while Porites sp. employed constitutive expression of all putative toxins regardless of active predation, suggesting a proactive defense strategy. Together, these findings suggest that preferred and non-preferred coral prey exhibit fundamentally different molecular and defensive strategies during CoTS predation, shedding light on the evolutionary arms race between corals and their predators.

molecular biology↗

Coral venom and toxins as protection against crown-of-thorns sea star attack

Crown-of-thorns sea star (CoTS) outbreaks are one of the leading causes of hard coral cover decline across the Indo-Pacific, posing a major threat to the health and resilience of coral reefs. However, the drivers underlying feeding on preferred (e.g., Acropora spp.) versus non-preferred (e.g., Porites spp.) are poorly understood. We hypothesised that coral venom may influence CoTS food preferences. We investigated whether coral venom toxin and peptide families may drive CoTS prey preferences by comparing the genomes and transcriptomes of preferred (five Acropora species) and non-preferred (five Porites species and Echinopora lamellosa) prey species of CoTS. We constructed databases of known cnidarian venom toxins, and along with the full UniProtKB/Swiss-Prot Tox-Prot database, used these to identify toxin peptides and investigate function and phylogeny. The most abundant toxins across all coral species included kunitz-type neurotoxins, neurotoxic turripeptides, snake venom lectins, toxic proteases and actinoporins. There were proteins present only in certain Porites species but completely absent from all Acropora species (e.g., tereporin/conoporin, snake venom peptides) and vice versa (e.g., sarafotoxin). Further, Porites species contained a homolog to conkunitzin, a toxin known to disintegrate the tube feet of CoTS, suggesting a potential mechanism for their lower susceptibility to predation. We also observed a greater diversity of jellyfish-like proteins in CoTS-exposed Porites species compared to naive Porites species, suggesting these proteins deter CoTS. These findings have direct applications to assessing reef corals susceptibility to future CoTS outbreaks and active reef management.

bioinformatics↗