Two hepcidin-like antimicrobial peptides in Barramundi Lates calcarifer exhibit differing tissue tropism and are induced in response to lipopolysaccharide

• Published in: Fish & shellfish immunology Vol. 31; no. 2; pp. 350 - 357
• Main Authors: Barnes, Andrew C., Trewin, Brendan, Snape, Natale, Kvennefors, E. Charlotte E., Baiano, Justice C.F.
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.08.2011
• Subjects: Amino Acid Sequence; Animals; Antimicrobial Cationic Peptides - chemistry; Antimicrobial Cationic Peptides - genetics; Antimicrobial Cationic Peptides - immunology; Antimicrobial Cationic Peptides - metabolism; Antimicrobial peptide; Base Sequence; DNA, Complementary - genetics; DNA, Complementary - immunology; DNA, Complementary - metabolism; Fish Proteins - genetics; Fish Proteins - immunology; Fish Proteins - metabolism; Gene Expression Profiling; Hepcidin; Hepcidins; Innate immunity; Lates calcarifer; Lipopolysaccharides - pharmacology; Micropterus; Molecular Sequence Data; Perciformes; Perciformes - genetics; Perciformes - immunology; Perciformes - metabolism; Pseudosciaena; Sebastes schlegeli; Innate immunity; Lates calcarifer; Hepcidin; Antimicrobial peptide
• ISSN: 1050-4648; 1095-9947
• DOI: 10.1016/j.fsi.2011.05.027

Genes encoding two hepcidin-like antimicrobial peptides were discovered in Barramundi, Lates calcarifer (barramundi, Giant sea perch). Analysis of the coding regions indicated that genes for each hepcidin comprised 3 exons and 2 introns. The deduced amino acid sequences for each molecule resulted in a protein comprising a signal sequence of 24 aa in each case, coupled to a prepropeptide of 75 aa for hepcidin 1 and 78 aa for hepcidin 2. A cleavage site was identified in each prepropetide at amino acid 64 with the cleavage motif – QKR/QS – resulting in mature peptides of 25 and 28 amino acids respectively. Each mature peptide contained 8 conserved cysteine residues and 3 dimensional modeling predicted a β-hairpin and β-sheet structure characteristic of human Liver Expressed Antimicrobial Peptide (LEAP). Analysis of the deduced amino acid sequences by BLAST with phylogenetic supported indicated that hepcidin 1 was a HAMP1-type peptide closely related to hepcidins identified in other Perciformes ( Micropterus and Pseudosciaena), whilst hepcidin 2 was a HAMP2-type peptide most similar to a hepcidin previously identified in black rock fish ( Sebastes schlegeli). Both hepcidin genes were inducible in barramundi following intraperitoneal injection with lipopolysaccharide, with elevated expression detected in liver and head kidney 3 h post IP injection for hepcidin 1 and in liver only for hepcidin 2. The elevated expression was transient with return to normal levels within 24–48 h. No significant expression of either peptide was detected in spleen, skin or gill following IP injection with LPS. ► Hepcidin-like antimicrobial peptides, Hepcidin 1 and 2 from Lates calcarifer are described. ► Phylogenetic analysis assigns them to HAMP1 and HAMP2-like hepcidins respectively. ► LPS up-regulated both hepcidins in the liver but only H1 in the head-kidney. ► Neither were detected in gill, spleen or skin.