Modified fish diet shifted serum metabolome and alleviated chronic anemia in bottlenose dolphins (Tursiops truncatus): Potential role of odd-chain saturated fatty acids

PLoS One. 2020 Apr 7;15(4):e0230769. doi: 10.1371/journal.pone.0230769. eCollection 2020.

Abstract

Bottlenose dolphins (Tursiops truncatus) are long-lived mammals that can develop chronic aging-associated conditions similar to humans, including metabolic syndrome. Initial studies suggest that these conditions may be attenuated in dolphins using a modified fish diet. Serum metabolomics, fatty acid panels, and blood-based health indices were compared between 20 dolphins on a modified, 50% wild-type diet (50% mullet, 25% capelin, and 25% squid and/or herring) and 10 dolphins on a baseline diet (75% capelin and 25% squid and/or herring). Blood samples were collected at Months 0, 1, 3 and 6. Dolphins on the modified diet had lower insulin (7.5 ± 4.0 and 14.8 ± 14.0 μIU/ml, P = 0.039), lower cholesterol (160 ± 26 and 186 ± 24 mg/dl, P = 0.015) and higher hematocrit (46 ± 3 and 44 ± 3%, P = 0.043) by Month 1 compared to controls. Dolphins with anemia (hemoglobin ≤ 12.5 g/dl, n = 6) or low-normal hemoglobin (12.5-13.5 g/dl, n = 3) before placed on the modified diet had normal hemoglobin concentrations (> 13.5 g/dl) by Month 3. The modified diet caused a significant shift in the metabolome, which included 664 known metabolites. Thirty prioritized metabolites at Months 1 and 3 were 100% predictive of dolphins on the modified diet. Among 25 prioritized lipids, 10 (40%) contained odd-chain saturated fatty acids (OCFAs); C15:0 was the highest-prioritized OCFA. Increased dietary intake of C15:0 (from 1.3 ± 0.4 to 4.5 ± 1.1 g/day) resulted in increased erythrocyte C15:0 concentrations (from 1.5 ± 0.3 to 5.8 ± 0.8 μg/ml, P < 0.0001), which independently predicted raised hemoglobin. Further, increasing age was associated with declining serum C15:0 (R2 = 0.14, P = 0.04). While higher circulating OCFAs have been previously associated with lower risks of cardiometabolic diseases in humans, further studies are warranted to assess potential active roles of OCFAs, including C15:0, in attenuating anemia.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Anemia / etiology*
  • Anemia / metabolism*
  • Animals
  • Bottle-Nosed Dolphin / blood*
  • Bottle-Nosed Dolphin / metabolism*
  • Cholesterol / metabolism
  • Diet / methods
  • Fatty Acids / metabolism*
  • Female
  • Fishes / blood*
  • Fishes / metabolism*
  • Male
  • Metabolic Syndrome / genetics
  • Metabolic Syndrome / metabolism
  • Metabolome / physiology*

Substances

  • Fatty Acids
  • Cholesterol

Grants and funding

This work was funded by a federal grant issued to SV by the Office of Naval Research (ONR Grant Number N000141512131, https://www.onr.navy.mil/). ONR had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Epitracker, Inc. provided support in the form of salaries for SV but did not have any role in the study design or data collection and analysis. Epitracker Inc. did play a role in the preparation of the manuscript and, in cooperation with the US Navy Marine Mammal Program, the decision to publish. The specific role of this author is articulated in the ‘author contributions’ section.