Ascorbic Acid Biosynthesis and Brackish Water Acclimation in the Euryhaline Freshwater White-Rimmed Stingray, Himantura signifer

PLoS One. 2013 Jun 18;8(6):e66691. doi: 10.1371/journal.pone.0066691. Print 2013.

Abstract

L-gulono-γ-lactone oxidase (Gulo) catalyzes the last step of ascorbic acid biosynthesis, which occurs in the kidney of elasmobranchs. This study aimed to clone and sequence gulonolactone oxidase (gulo) from the kidney of the euryhaline freshwater stingray, Himantura signifer, and to determine the effects of acclimation from freshwater to brackish water (salinity 20) on its renal gulo mRNA expression and Gulo activity. We also examined the effects of brackish water acclimation on concentrations of ascorbate, dehydroascorbate and ascorbate + dehydroascorbate in the kidney, brain and gill. The complete cDNA coding sequence of gulo from the kidney of H. signifer contained 1323 bp coding for 440 amino acids. The expression of gulo was kidney-specific, and renal gulo expression decreased significantly by 67% and 50% in fish acclimated to brackish water for 1 day and 6 days, respectively. There was also a significant decrease in renal Gulo activity after 6 days of acclimation to brackish water. Hence, brackish water acclimation led to a decrease in the ascorbic acid synthetic capacity in the kidney of H. signifer. However, there were significant increases in concentrations of ascorbate and ascorbate + dehydroascorbate in the gills (after 1 or 6 days), and a significant increase in the concentration of ascorbate and a significant decrease in the concentration of dehydroascorbate in the brain (after 1 day) of fish acclimated to brackish water. Taken together, our results indicate that H. signifer might experience greater salinity-induced oxidative stress in freshwater than in brackish water, possibly related to its short history of freshwater invasion. These results also suggest for the first time a possible relationship between the successful invasion of the freshwater environment by some euryhaline marine elasmobranchs and the ability of these elasmobranchs to increase the capacity of ascorbic acid synthesis in response to hyposalinity stress.

MeSH terms

  • Adaptation, Physiological
  • Amino Acid Sequence
  • Animals
  • Ascorbic Acid / biosynthesis*
  • Ascorbic Acid / metabolism
  • Base Sequence
  • Fresh Water*
  • Phylogeny
  • Sequence Homology, Amino Acid
  • Skates, Fish / genetics
  • Skates, Fish / metabolism*
  • Skates, Fish / physiology
  • Tissue Distribution

Substances

  • Ascorbic Acid

Grants and funding

This study was supported in part by the Singapore Ministry of Education through grant R154-000-470-112 and the Singapore Ministry of Defence through grant R-347-000-188-232 to Y. K. Ip. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.