Nile tilapia TBK1 interacts with STING and TRAF3 and is involved in the IFN-β pathway in the immune response

• Published in: Fish & shellfish immunology 2023-11, Vol.142, p.109125-109125, Article 109125
• Main Authors: Zheng, Qiuyue, Gao, Fengying, Liu, Zhigang, Sun, Chengfei, Dong, Junjian, Zhang, Hetong, Ke, Xiaoli, Lu, Maixin
• Format: Article
• Language: English
• Subjects: Expression profile; Immune response; Nile tilapia (Oreochromis niloticus); TBK1
• ISSN: 1050-4648; 1095-9947
• DOI: 10.1016/j.fsi.2023.109125

Nile tilapia (Oreochromis niloticus) occupies an important position in the culture of economic fish in China. However, the high mortality caused by streptococcal disease has had a significant impact on the tilapia farming industry. Therefore, it is necessary to clarify the immune mechanism of tilapia in response to Streptococcus agalactiae. As a hub in the natural immune signaling pathway, the junction molecule can help the organism defend against and clear pathogens and is crucial in the signaling pathway. In this study, the cDNA sequence of Nile tilapia TBK1 was cloned, and the expression profile was examined in normal fish and challenged fish. The cDNA sequence of the TBK1 gene was 3378 bp, and its open reading frame (ORF) was 2172 bp, encoding 723 amino acids. The deduced TBK1 protein contained an S_TKc domain, a coiled coil domain and a ubiquitin-like domain (ULD). TBK1 had the highest homology with zebra mbuna (Maylandia zebra) and Lake Malawi cichlid fish (Astatotilapia calliptera), both at 97.59%. In the phylogenetic tree, TBK1 forms a large branch with other scleractinian fish. TBK1 expression was highest in the brain and lowest in the liver. LPS, Poly I:C, and S. agalactiae challenge resulted in significant changes in TBK1 expression in the tissues examined. The subcellular localization showed that TBK1-GFP was distributed in the cytoplasm and could significantly increase IFN-β activation. Pull-down results showed that there was an interaction between TBK1 and TRAF3 and an interaction between STING protein and TBK1 protein. The above results provide a basis for further investigation into the mechanism of TBK1 involvement in the signaling pathway. •The cDNA sequence of TBK1 was identified from tilapia (Oreochromis niloticus).•Stimulation of S. agalactiae, PolyI:C and LPS can change gene expression level of TBK1.•The overexpression of TBK1 significantly induced the NF-kappaB activity in cell line.•The TBK1 interacted with STING and TRAF3.