Targeted metabolomics characterizes metabolite occurrence and variability in stable freshwater mussel populations

Author:

Waller Diane1ORCID,Putnam Joel2ORCID,Steiner J Nolan1,Fisher Brant3,Burcham Grant N4ORCID,Oliver John1,Smith Stephen B5,Erickson Richard1ORCID,Remek Anne6,Bodoeker Nancy7

Affiliation:

1. United States Geological Survey, Upper Midwest Environmental Sciences Center , 2630 Fanta Reed Road, La Crosse, WI 54603, USA

2. Conagen, Inc. , 15 Deangelo Dr, Bedford, MA 01730, USA

3. Indiana Department of Natural Resources – Division of Fish & Wildlife , Atterbury Fish & Wildlife Area, 7970 South Rowe Street, Edinburgh, IN  46124, USA

4. Heeke Animal Disease Diagnostic Laboratory , 11367 East Purdue Farm Road, Dubois, IN 47527 and Department of Comparative Pathobiology, College of Veterinary Medicine, Purdue University, West Lafayette, IN 47907, USA

5. Department of Animal Science, Texas A&M University , 2471 TAMU, College Station, TX 77843, USA

6. 200 W Washington St, Indianapolis , IN 46204, USA

7. Department of Comparative Pathobiology, Purdue University College of Veterinary Medicine , 625 Harrison St. West Lafayette, IN 47907, USA

Abstract

Abstract Freshwater mussels (order Unionida) play a key role in freshwater systems as ecosystem engineers and indicators of aquatic ecosystem health. The fauna is globally imperilled due to a diversity of suspected factors; however, causes for many population declines and mortality events remain unconfirmed due partly to limited health assessment tools. Mussel-monitoring activities often rely on population-level measurements, such as abundance and age structure, which reflect delayed responses to environmental conditions. Measures of organismal health would enable preemptive detection of declining condition before population-level effects manifest. Metabolomic analysis can identify shifts in biochemical pathways in response to stressors and changing environmental conditions; however, interpretation of the results requires information on inherent variability of metabolite concentrations in mussel populations. We targeted metabolites in the haemolymph of two common mussels, Lampsilis cardium and Lampsilis siliquoidea, from three Indiana streams (USA) using ultra-high-performance liquid chromatography combined with quadrupole time-of-flight mass spectroscopy. The influence of species, stream and sex on metabolite variability was examined with distance-based redundancy analysis. Metabolite variability was most influenced by species, followed by site and sex. Inter- and intraspecies metabolite variability among sexes was less distinct than differences among locations. We further categorized metabolites by occurrence and variability in mussel populations. Metabolites with high occurrence (Categories 1 and 2) included those indicative of energy status (catabolism versus anabolism; arginine, proline, carnitine, nicotinic acid, pantothenic acid), oxidative stress (proline, glutamine, glutamate) and protein metabolism (thymidine, cytidine, inosine). Metabolites with lower occurrence (Category 3) are constituents of assorted metabolic pathways and can be important biomarkers with additional temporal sampling to characterize their variability. These data provide a reference for future temporal (before/after) monitoring and for studies of stressor–metabolite linkages in freshwater mussels.

Publisher

Oxford University Press (OUP)

Subject

Management, Monitoring, Policy and Law,Nature and Landscape Conservation,Ecological Modeling,Physiology

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