{"title":"Transferrin from obscure puffer Takifugu obscurus promotes antimicrobial immune response","authors":"Ruixia Wang, Ying Huang, Yan Shi, Zhe Zhao","doi":"10.1016/j.fsi.2025.110184","DOIUrl":null,"url":null,"abstract":"<div><div>Transferrin (TF) is an iron-binding glycoprotein that plays a crucial role in host defense by restricting iron availability to pathogens and activating antimicrobial immune responses. However, its antimicrobial role in fish remains largely unexplored. In this study, we identified and characterized transferrin from obscure puffer <em>Takifugu obscurus</em>, named ToTF, and investigated its functions in bacterial infections. The coding region of the ToTF gene consists of 2295 bp, encoding a polypeptide of 764 amino acids. Tissue distribution analysis revealed that <em>ToTF</em> is primarily expressed in the liver. The mRNA expression of ToTF was significantly upregulated in both the liver and kidney following challenge with <em>Staphylococcus aureus</em> and <em>Vibrio harveyi</em>. Moreover, recombinant ToTF (rToTF) markedly inhibits iron-dependent bacteria growth, including <em>S. aureus</em> and <em>V. harveyi</em>. The iron-binding capacity of rToTF peaked at pH 8 and decreased significantly under acidic conditions. Furthermore, the antibacterial activity of rToTF peaked at near-neutral pH but decreased significantly at pH below 5. This dual mechanism deprives bacteria of essential iron through high-affinity binding and directly inhibits their growth under optimal conditions. These findings highlight the dual role of ToTF in the antibacterial immunity of <em>T. obscurus</em>, mediated by iron sequestration and direct bacteriostatic effects. This study supports the development of TF-based antibacterial agents and enhances strategies for aquatic disease prevention and fish disease resistance.</div></div>","PeriodicalId":12127,"journal":{"name":"Fish & shellfish immunology","volume":"159 ","pages":"Article 110184"},"PeriodicalIF":4.1000,"publicationDate":"2025-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fish & shellfish immunology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1050464825000737","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"FISHERIES","Score":null,"Total":0}
引用次数: 0
Abstract
Transferrin (TF) is an iron-binding glycoprotein that plays a crucial role in host defense by restricting iron availability to pathogens and activating antimicrobial immune responses. However, its antimicrobial role in fish remains largely unexplored. In this study, we identified and characterized transferrin from obscure puffer Takifugu obscurus, named ToTF, and investigated its functions in bacterial infections. The coding region of the ToTF gene consists of 2295 bp, encoding a polypeptide of 764 amino acids. Tissue distribution analysis revealed that ToTF is primarily expressed in the liver. The mRNA expression of ToTF was significantly upregulated in both the liver and kidney following challenge with Staphylococcus aureus and Vibrio harveyi. Moreover, recombinant ToTF (rToTF) markedly inhibits iron-dependent bacteria growth, including S. aureus and V. harveyi. The iron-binding capacity of rToTF peaked at pH 8 and decreased significantly under acidic conditions. Furthermore, the antibacterial activity of rToTF peaked at near-neutral pH but decreased significantly at pH below 5. This dual mechanism deprives bacteria of essential iron through high-affinity binding and directly inhibits their growth under optimal conditions. These findings highlight the dual role of ToTF in the antibacterial immunity of T. obscurus, mediated by iron sequestration and direct bacteriostatic effects. This study supports the development of TF-based antibacterial agents and enhances strategies for aquatic disease prevention and fish disease resistance.
期刊介绍:
Fish and Shellfish Immunology rapidly publishes high-quality, peer-refereed contributions in the expanding fields of fish and shellfish immunology. It presents studies on the basic mechanisms of both the specific and non-specific defense systems, the cells, tissues, and humoral factors involved, their dependence on environmental and intrinsic factors, response to pathogens, response to vaccination, and applied studies on the development of specific vaccines for use in the aquaculture industry.