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Edwards, O. R.

Publications and source records attributed to Edwards, O. R..

2 recordsLinked to original sources

Rapid thermal adaptation in coral photosymbionts draws on standing variation and recombination

Bleaching tolerance in corals depends in part on the thermal tolerance of their microalgal symbionts. Laboratory evolution has increased the thermal tolerance of the symbiont Cladocopium proliferum in ~120 generations, but the genetic basis of that response was unknown. We compared single nucleotide polymorphisms in transcriptomes of three heat-evolved C. proliferum strains and one wild-type (unselected) strain from the same progenitor. We found 15,640 polymorphic loci, but no variant was both private to a strain and consistent across its replicates, which indicates that new mutations contributed little to the response in expressed sequences. Instead, allele frequencies at 350 loci differed significantly between strains, and linkage patterns indicated recombination had occurred within scaffolds both before and after the strains were separated. Selection and recombination of variation already present in the progenitor therefore underpinned the rapid thermal adaptation. Experimental evolution for reef restoration should start from genetically diverse cultures rather than single cell isolates.

evolutionary biology↗

Flow cytometry-based biomarker assay for in vitro identification of heat tolerance conferring coral symbionts

Corals tolerance to high temperature stress largely depends on their symbiotic microalgae (Symbiodiniaceae). However, the contributing microalgal traits are largely unclear. Here we compare the in vitro cellular profiles of seven Cladocopium C1acro microalgal strains (derived from the same ancestral strain) during a four-week exposure to 27{degrees}C or 31{degrees}C. One was an unselected wild-type strain (WT), three were selected at 31{degrees}C for nine years and shown to confer thermal tolerance on the coral host (SS+) and three others were similarly selected but did not confer tolerance (SS-). Flow cytometry was used to measure the intracellular stress indicators reactive oxygen species (ROS), reduced glutathione (rGSH) and mitochondrial-membrane potential ({Delta}{Psi}m), as well as cell size/shape and photosynthetic pigments. Cell densities and photosynthetic efficiency ({Phi}PSII, Fv/Fm) were also measured. WT showed the highest levels of intracellular ROS and {Delta}{Psi}m, lowest rGSH and largest cell sizes at both temperatures. SS+ strains had the lowest ROS and highest rGSH values and a unique pattern of correlations among parameters at 31{degrees}C. Our results support previous reports implicating the role of microalgal ROS, {Delta}{Psi}m and rGSH in holobiont thermal tolerance and suggest flow cytometry is a useful pre-screening tool for identifying microalgal strains with enhanced thermal tolerance.

microbiology↗