Signaling events induced by lipopolysaccharide-activated Toll in response to bacterial infection in shrimp.
Signaling events induced by lipopolysaccharide-activated Toll in response to bacterial infection in shrimp.
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DOI:
10.3389/fimmu.2023.1119879
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发表时间:
2023
影响因子:
7.3
通讯作者:
Li, Chaozheng
中科院分区:
文献类型:
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作者:
Wang, Sheng;Li, Haoyang;Li, Qinyao;Yin, Bin;Li, Sedong;He, Jianguo;Li, Chaozheng
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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影响因子:
6.7
作者:
Mitri C;Jacques JC;Thiery I;Riehle MM;Xu J;Bischoff E;Morlais I;Nsango SE;Vernick KD;Bourgouin C
通讯作者:
Bourgouin C
影响因子:
64.5
作者:
Chevrier N;Mertins P;Artyomov MN;Shalek AK;Iannacone M;Ciaccio MF;Gat-Viks I;Tonti E;DeGrace MM;Clauser KR;Garber M;Eisenhaure TM;Yosef N;Robinson J;Sutton A;Andersen MS;Root DE;von Andrian U;Jones RB;Park H;Carr SA;Regev A;Amit I;Hacohen N
通讯作者:
Hacohen N
影响因子:
29.7
作者:
Brubaker SW;Bonham KS;Zanoni I;Kagan JC
通讯作者:
Kagan JC
影响因子:
64.8
作者:
Alexopoulou, L;Holt, AC;Flavell, RA
通讯作者:
Flavell, RA
影响因子:
11
作者:
通讯作者:
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