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Veterinary immunology and immunopathology2009; 135(1-2); 34-42; doi: 10.1016/j.vetimm.2009.10.027

Cloning, sequencing and expression analysis of the equine hepcidin gene by real-time PCR.

Abstract: Equine serum or plasma iron concentration drops quickly during inflammation. Accumulation of iron inside macrophages and reduction of the intestinal absorption of this element cause hypoferremia during systemic inflammatory processes. These mechanisms are mediated by hepcidin, a 25 amino acids peptide synthesized mainly in the liver in response to iron stores and inflammation. Hepcidin is an important peptide for systemic iron homeostasis and also has antibacterial and antifungal activities. Hepcidin up-regulation is particularly useful during acute inflammation, especially before adaptive immunity occurs, restricting iron availability necessary for pathogenic microorganism growth. Hepcidin gene products have been previously characterized in man, non-human primates, rat, mouse, dog swine, cattle, fishes, reptiles and birds; but until now not in the horse. We have cloned and sequenced equine hepcidin mRNA and performed hepcidin expression analysis in different tissues collected from four healthy horses. The deduced precursor of equine hepcidin was most homologous to Bos taurus and Sus scrofa. The expressed profile of equine hepcidin in liver was very high. Expression in cervical spinal cord and cerebral cortex was much lower than liver but higher than lung, duodenum, stomach, spleen, kidney, skeletal muscle and bladder. This sequence will be helpful for additional studies on iron metabolism and inflammatory process in horses.
Publication Date: 2009-11-02 PubMed ID: 19945753DOI: 10.1016/j.vetimm.2009.10.027Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research paper discusses the cloning, sequencing and expression analysis of the equine hepcidin gene. Essentially, the researchers have isolated and studied the horse gene associated with regulating iron levels and responding to inflammation, known as hepcidin.

Primary Focus of the Research

  • The primary focus of the research is the equine hepcidin gene. Hepcidin is a peptide that controls iron levels in the body and plays an essential role in the systemic iron homeostasis, which is crucial to an organisms overall wellbeing. This peptide is also known for its antibacterial and antifungal properties.
  • Notably, during periods of inflammation, the body’s iron concentration drops dramatically: the hepcidin peptide mediates this, causing an accumulation of iron inside macrophages and the decreased absorption of iron in the intestines.

Why this Research?

  • Though the hepcidin gene has been characterized in numerous organisms—men, non-human primates, rats, mice, dogs, swine, cattle, fish, reptiles and birds—it has not been previously studied in a horse.
  • This research is essential as it expands our understanding of iron metabolism and inflammation across a broad spectrum of species, including horses. The horse’s hepcidin gene could differ in many ways, influencing how iron is regulated and how inflammation is handled in this species.

Methodology and Findings

  • The researchers cloned and sequenced equine hepcidin mRNA from four healthy horses. They then performed an expression analysis in various tissues from these horses.
  • The precursor of equine hepcidin was found to be most homologous to Bos taurus (cattle) and Sus scrofa (pig).
  • The expression of hepcidin in horse liver was very high compare to other tissues. In contrast, its expression in the cervix spinal cord and cerebral cortex was much lower than in the liver but higher than in the lung, duodenum, stomach, spleen, kidney, skeletal muscle, and bladder.

Potential Implications

  • This sequence discovery will be valuable for future studies on iron metabolism and the inflammatory process in horses, possibly leading to better disease prevention and treatment strategies for this species.

Cite This Article

APA
Oliveira Filho JP, Badial PR, Cunha PHJ, Cruz TF, Araújo JP, Divers TJ, Winand NJ, Borges AS. (2009). Cloning, sequencing and expression analysis of the equine hepcidin gene by real-time PCR. Vet Immunol Immunopathol, 135(1-2), 34-42. https://doi.org/10.1016/j.vetimm.2009.10.027

Publication

ISSN: 1873-2534
NlmUniqueID: 8002006
Country: Netherlands
Language: English
Volume: 135
Issue: 1-2
Pages: 34-42
PII: S0165-2427(09)00353-5

Researcher Affiliations

Oliveira Filho, José P
  • Department of Veterinary Clinical Science, School of Veterinary Medicine and Animal Science, Sao Paulo State University, Unesp, FMVZ, Botucatu, SP 18618000, Brazil.
Badial, Peres R
  • Department of Veterinary Clinical Science, School of Veterinary Medicine and Animal Science, Sao Paulo State University, Unesp, FMVZ, Botucatu, SP 18618000, Brazil.
Cunha, Paulo H J
  • Department of Veterinary Clinical Science, School of Veterinary Medicine and Animal Science, Sao Paulo State University, Unesp, FMVZ, Botucatu, SP 18618000, Brazil.
Cruz, Taís F
  • Department of Immunology and Microbiology, Sao Paulo State University, Unesp, IBB, Botucatu, SP 18618000, Brazil.
Araújo, João P
  • Department of Immunology and Microbiology, Sao Paulo State University, Unesp, IBB, Botucatu, SP 18618000, Brazil.
Divers, Thomas J
  • Department of Clinical Science, Cornell University, Ithaca, NY 14853, USA.
Winand, Nena J
  • Department of Molecular Medicine, Cornell University, Ithaca, NY 14853, USA.
Borges, Alexandre S
  • Department of Veterinary Clinical Science, School of Veterinary Medicine and Animal Science, Sao Paulo State University, Unesp, FMVZ, Botucatu, SP 18618000, Brazil. Electronic address: asborges@fmvz.unesp.br.

MeSH Terms

  • Amino Acid Sequence
  • Animals
  • Antimicrobial Cationic Peptides / genetics
  • Base Sequence
  • Cloning, Molecular
  • DNA, Complementary / genetics
  • Gene Expression Profiling
  • Hepcidins
  • Horses / genetics
  • Liver / metabolism
  • Molecular Sequence Data
  • Open Reading Frames / genetics
  • Phylogeny
  • Reverse Transcriptase Polymerase Chain Reaction / veterinary
  • Sequence Alignment
  • Sequence Analysis, DNA

Citations

This article has been cited 5 times.
  1. Satué K, Fazio E, La Fauci D, Medica P. Changes of Hepcidin, Ferritin and Iron Levels in Cycling Purebred Spanish Mares. Animals (Basel) 2023 Mar 31;13(7).
    doi: 10.3390/ani13071229pubmed: 37048485google scholar: lookup
  2. Mira J, Herman M, Zakia LS, Olivo G, Araújo JP Jr, Borges AS, Oliveira-Filho JP. Frequency of Equus caballus papillomavirus in equine aural plaques. J Vet Diagn Invest 2018 Jul;30(4):565-568.
    doi: 10.1177/1040638717753495pubmed: 29601778google scholar: lookup
  3. Lombardi L, Maisetta G, Batoni G, Tavanti A. Insights into the antimicrobial properties of hepcidins: advantages and drawbacks as potential therapeutic agents. Molecules 2015 Apr 10;20(4):6319-41.
    doi: 10.3390/molecules20046319pubmed: 25867823google scholar: lookup
  4. Bruhn O, Grötzinger J, Cascorbi I, Jung S. Antimicrobial peptides and proteins of the horse--insights into a well-armed organism. Vet Res 2011 Sep 2;42(1):98.
    doi: 10.1186/1297-9716-42-98pubmed: 21888650google scholar: lookup
  5. Khangembam VC, Kumar A. Buffalo hepcidin: characterization of cDNA and study of antimicrobial property. Vet Res Commun 2011 Feb;35(2):79-87.
    doi: 10.1007/s11259-010-9452-8pubmed: 21161377google scholar: lookup