Frontiers in Immunology (Feb 2023)

Signaling events induced by lipopolysaccharide-activated Toll in response to bacterial infection in shrimp

  • Sheng Wang,
  • Sheng Wang,
  • Sheng Wang,
  • Haoyang Li,
  • Haoyang Li,
  • Haoyang Li,
  • Qinyao Li,
  • Qinyao Li,
  • Bin Yin,
  • Bin Yin,
  • Sedong Li,
  • Jianguo He,
  • Jianguo He,
  • Jianguo He,
  • Jianguo He,
  • Chaozheng Li,
  • Chaozheng Li,
  • Chaozheng Li,
  • Chaozheng Li

DOI
https://doi.org/10.3389/fimmu.2023.1119879
Journal volume & issue
Vol. 14

Abstract

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Toll-like receptors (TLR) play a crucial role in the detection of microbial infections in vertebrates and invertebrates. Mammalian TLRs directly recognize a variety of structurally conserved microbial components. However, invertebrates such as Drosophila indirectly recognize microbial products by binding to the cytokine-like ligand Spätzle, which activates signaling cascades that are not completely understood. In this study, we investigated the signaling events triggered by Toll in response to lipopolysaccharide (LPS), a cell wall component of gram-negative bacteria, and Vibrio parahaemolyticus infection in the arthropod shrimp Litopenaeus vannamei. We found that five of the nine Tolls from L. vannamei bound to LPS and the RNAi of LvToll1, LvToll2, LvToll3, LvToll5, and LvToll9 weakened LvDorsal-L phosphorylation induced by V. parahaemolyticus. All nine Tolls combined with MyD88 via the TIR domain, thereby conferring signals to the tumor necrosis factor receptor-associated factor 6 (TRAF6)-transforming growth factor-β activated kinase 1 binding protein 2 (TAB2)-transforming growth factor-β activated kinase 1 (TAK1) complex. Further examination revealed that the LvTRAF6-LvTAB2-LvTAK1 complex contributes to Dorsal-L phosphorylation and nuclear translocation during V. parahaemolyticus infection. Overall, shrimp Toll1/2/3/5/9–TRAF6/TAB2/TAK1–Dorsal cascades protect the host from V. parahaemolyticus infection, which provides a better understanding of how the innate immune system recognizes and responds to bacterial infections in invertebrates.

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