Catfish hepcidin gene is expressed in a wide range of tissues and exhibits tissue-specific upregulation after bacterial infection
DNA, Complementary
Base Sequence
Molecular Sequence Data
Enterobacteriaceae Infections
04 agricultural and veterinary sciences
Edwardsiella ictaluri
Immunity, Innate
Up-Regulation
3. Good health
Ictaluridae
Fish Diseases
Hepcidins
Species Specificity
Organ Specificity
Sepsis
Animals
Humans
0401 agriculture, forestry, and fisheries
Amino Acid Sequence
Catfishes
Antimicrobial Cationic Peptides
DOI:
10.1016/j.dci.2005.03.006
Publication Date:
2005-05-05T12:01:14Z
AUTHORS (5)
ABSTRACT
Antimicrobial peptides (AMPs) are important components of the host innate immune response against microbial invasion. The cysteine-rich AMPs such as defensin and hepcidin have been extensively studied from various organisms, but their role in disease defense in catfish is unknown. As a first step, we sequenced a hepcidin cDNA from both channel catfish and blue catfish, and characterized the channel catfish hepcidin gene. The channel catfish hepcidin gene consists of two introns and three exons that encode a peptide of 96 amino acids. The amino acid sequences and gene organization were conserved between catfish and other organisms. In contrast to its almost exclusive expression in the liver in humans, the channel catfish hepcidin gene was expressed in a wide range of tissues except brain. Its expression was detected early during embryonic and larval development, and induced after bacterial infection with Edwardsiella ictaluri, the causative agent of enteric septicemia of catfish (ESC) in a tissue-specific manner. The upregulation was observed in the spleen and head kidney, but not in the liver. The expression of hepcidin was upregulated 1--3 days after challenge, but returned to normal levels at 7 days after challenge. The expression profile of the catfish hepcidin gene during the course of bacterial infection mirrors those of inflammatory proteins such as chemokines, suggesting an important role for hepcidin during inflammatory responses.
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