Development of a widely applicable immunoassay for insulin in marine teleosts that regulates cross-reactivity using biotinylation and inhibits interference by plasma components

• An immunoassay for measuring insulin in teleosts was developed.
• This assay can be applicable to at least 6 teleosts that are phylogenetically far.
• The applicability was achieved by regulating immunoreactivity in a labeled ligand.
• This is the first report of plasma interference in insulin immunoassay in fish.
• Novel simple methods for inhibition of this interference were also developed.

Amino acids are important insulinotropins in fish, and their effects vary between amino acids and fish species. Insulin levels are indicative of growth efficiency and stress levels in fish; however, interspecies comparisons of insulin levels are hampered by the difficulty of measuring insulin concentration in each fish. We developed a widely applicable competitive immunoassay using biotinylated yellowtail (Seriola quinqueradiata) insulin for measuring insulin in marine teleosts, including yellowtail and red seabream (Pagrus major), which are the most common species raised by aquaculture in Japan. Amino acid sequence substitution was limited at the ninth residue of the A-chain (A9) between these two species, and analysis of the primary structures of insulins from six phylogenetically far teleosts suggested that the sequences of yellowtail and red seabream insulins are identical to those of many teleosts, except the A9 residue. However, A9 is known to be an epitope that confers cross-reactive differences on insulin. We solved this problem through immunoreactive invalidation of this residue by biotinylation. The binding–inhibition curves of yellowtail and red seabream insulins were identical following the use of this technique. However, yellowtail and red seabream plasma was found to contain components that interfere with immunoassays. This problem was solved by the extraction of plasma using equal volume of acid–ethanol in yellowtail and by cooling at 0 °C during the cross-reaction between the ligand and antibody in red seabream. Serially diluted plasma samples from both species exhibited linearity after these treatments. In a recovery test using plasma with added yellowtail insulin, the average recovery varied from 96.2% to 109.4%. A post-feeding rise in insulin was confirmed by this immunoassay in yellowtail, and peak of the rise was 39.8 ± 7 ng/ml at 1 h postfeeding from 3.9 ± 1.1 ng/ml at 0 h. This indicates that this assay is sufficient for measuring the baseline concentration of plasma insulin after starvation and is a useful indicator of nutritional status in yellowtail, as in other teleosts. This immunoassay demonstrated high performance and resisted interference from plasma components; consequently, it constitutes a useful tool for the interspecies evaluation of insulinotropins and represents a widely applicable insulin immunoassay for many teleosts.