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Cold stress syndrome (CSS) in the Florida manatee (Trichechus manatus latirostris) results in perturbations to many physiological pathways, often leading to further illness or death. In this study, we applied a non-targeted lipidomics approach with ultra-high performance liquid chromatography and high-resolution tandem mass spectrometry to characterize changes related to CSS in the lipidomic profiles of manatee plasma. Lipidomic analyses were conducted on healthy manatee (control) and cold-exposed manatee plasma samples with varying concentrations of Serum Amyloid A (SAA), an acute-phase protein that is associated with inflammatory disease. Control manatees (n = 10) were compared to all manatees exposed to cold temperatures (n = 17), and a subset of those manatees with SAA values > 120 [mu]g/mL (n = 9). Increased SAA values were associated with higher levels of various acylcarnitine lipids, while several triacylglycerols and oxidized triacylglycerols were significantly lower in manatees with cold exposure. These identified lipids are critical molecules involved in the maintenance of energy homeostasis and could potentially be examined in conjunction with current physical parameters to characterize cold stress. The ability to detect such differences highlights the addition of lipidomics as a valuable tool in understanding cold stress and potentially other illnesses in manatees. Further investigation into the function of the altered lipids could greatly increase our understanding of lipid metabolism in physiologically stressed manatees as well as other marine mammals and inform future management recovery strategies., Author(s): Emily K. Griffin [sup.1] , Kaylie Anne Costa [sup.1] , Juan J. Aristizabal-Henao [sup.1] , Michael P. Napolitano [sup.2] , Margaret E. Hunter [sup.3] , Jason A. Ferrante [sup.3] [...]

In recent years, the utility of lipidomics has been recognized in environmental toxicology and biomonitoring efforts due to the ubiquitous nature and importance of lipids in many cellular processes including signal transduction, energy storage, and cellular compartmentalization. Additionally, technological advances in high-resolution mass spectrometry have enabled the rapid expansion of the field, creating a surge in interest in comparative studies of lipid metabolism from a Systems Biology standpoint. Here, we adapted a nontargeted lipidomic approach for the study of plasma samples from nesting female leatherback (Dermochelys coriacea), loggerhead (Caretta caretta), and green (Chelonia mydas) sea turtles in Florida using ultra-high-performance liquid chromatography/high-resolution tandem mass spectrometry. We identified 877 lipids in common between the three species, of which the concentrations for 467 lipids were statistically different between two or more group comparisons. Principal component analysis revealed unique lipidomic signatures associated with each species of turtle, including various glycerophosphatidylcholines, glycerophosphatidylethanolamines, triacylglycerols, and oxidized triacylglycerols that were higher in leatherback sea turtles, diacylglycerols and select glycerophosphatidylinositols which were higher in loggerhead sea turtles, and specific plasmanyl-phosphatidylcholines that were higher in green sea turtles. Our results indicate that lipidomic profiling can be a useful tool for studying lipid metabolism and physiology of different species of sea turtles, while establishing baseline data that may be used as reference in future studies for observation of differences in life stages, for following spatial and temporal trends in nesting turtles, and for investigating population dynamics in response to various stressors., Author(s): Atiye Ahmadireskety [sup.1], Juan J. Aristizabal-Henao [sup.2], Anna Marqueño [sup.3], Justin R. Perrault [sup.4], Nicole I. Stacy [sup.5], Charles A. Manire [sup.4], John A. Bowden [sup.1] [sup.2] Author Affiliations: [...]