Teleost-specific TLR23 in Takifugu rubripes recruits MyD88 to trigger ERK pathway and promotes antibacterial defense

Fish Shellfish Immunol. 2024 Aug:151:109724. doi: 10.1016/j.fsi.2024.109724. Epub 2024 Jun 26.

Abstract

Takifugu rubripes is a highly valued cultured fish in Asia, while pathogen infections can result in severe diseases and lead to substantial economic losses. Toll-like receptors (TLRs), as pattern recognition receptors, play a crucial role on recognition pathogens and initiation innate immune response. However, the immunological properties of teleost-specific TLR23 remain largely unknown. In this study, we investigated the biological functions of TLR23 (TrTLR23) from T. rubripes, found that TrTLR23 existed in various organs. Following bacterial pathogen challenge, the expression levels of TrTLR23 were significantly increased in immune related organs. TrTLR23 located on the cellular membrane and specifically recognized pathogenic microorganism. Co-immunoprecipitation and antibody blocking analysis revealed that TrTLR23 recruited myeloid differentiation primary response protein (MyD88), thereby mediating the activation of the ERK signaling pathway. Furthermore, in vivo showed that, when TrTLR23 is overexpressed in T. rubripes, bacterial replication in fish tissues is significantly inhibited. Consistently, when TrTLR23 expression in T. rubripes is knocked down, bacterial replication is significantly enhanced. In conclusion, these findings suggested that TrTLR23 played a critical role on mediation TLR23-MyD88-ERK axis against bacterial infection. This study revealed that TLR23 involved in the innate immune mechanism, and provided the foundation for development disease control strategies in teleost.

Keywords: Bacterial infection; TLR23; Takifugu rubripes; Toll-like receptor.

MeSH terms

  • Animals
  • Edwardsiella / immunology
  • Edwardsiella / physiology
  • Fish Diseases* / immunology
  • Fish Proteins* / genetics
  • Fish Proteins* / immunology
  • Gene Expression Regulation / immunology
  • Immunity, Innate* / genetics
  • MAP Kinase Signaling System / immunology
  • Myeloid Differentiation Factor 88* / genetics
  • Myeloid Differentiation Factor 88* / immunology
  • Myeloid Differentiation Factor 88* / metabolism
  • Takifugu* / genetics
  • Takifugu* / immunology
  • Toll-Like Receptors* / genetics
  • Toll-Like Receptors* / immunology
  • Toll-Like Receptors* / metabolism
  • Vibrio / physiology

Substances

  • Fish Proteins
  • Myeloid Differentiation Factor 88
  • Toll-Like Receptors