Characterization and Immune Function of NOD1 in Snakehead (Channa argus)
The innate immune response is a critical defense mechanism by which vertebrates recognize and eliminate invading pathogens. Pattern recognition receptors (PRRs) detect pathogen-associated molecular patterns and activate downstream signaling pathways. NOD1, a classic PRR of the NLR family, recruits the adaptor protein RIPK2 to initiate antibacterial signaling. In this study, we cloned and characterized the NOD1 gene from snakehead (Channa argus). Briefly, the full-length NOD1 cDNA is 2829 bp encoding 943 amino acids, showing high homology with Perciformes. The qPCR analysis revealed widespread NOD1 gene expression in various tissues, with significant upregulation in the gill (p < 0.05) and spleen (p < 0.05) following bacterial infection. Overexpression of the NOD1 gene activated the NF-κB signaling pathway in a dose- and time-dependent manner, and specifically responded to the bacterial ligand iE-DAP but not to other tested ligands. Furthermore, NOD1 synergized with the downstream adaptor RIPK2 to enhance NF-κB activity, and direct protein interaction between NOD1 and RIPK2 was confirmed by co-immunoprecipitation. Taken together, these findings demonstrate that snakehead NOD1 plays a critical role in the host antimicrobial immune response.
Authors
- YJ Li
- Ning Yang (ORCID: https://orcid.org/0000-0001-5772-3320)
- Qiang Fu (ORCID: https://orcid.org/0000-0002-9094-5168)
- Chao Li (ORCID: https://orcid.org/0000-0002-1950-0190)
- Beibei Wang (ORCID: https://orcid.org/0000-0003-2362-2905)
- Xiaoyan Zhang (ORCID: https://orcid.org/0000-0002-3193-1401)
- Liu Y (ORCID: https://orcid.org/0009-0004-3901-1652)
- Min Cao (ORCID: https://orcid.org/0009-0008-1354-2921)
- Guangzhou Wu (ORCID: https://orcid.org/0009-0007-2424-1414)
- Xiaochen Zhu
Institutions
- Qingdao Agricultural University (CN)
- Jining University (CN)
Publication Details
- Journal
- Biology
- Published
- 2026-06-16
- DOI
- https://doi.org/10.3390/biology15120942
- Primary Topic
- Immune Response and Inflammation
- Type
- article
- Field-Weighted Citation Impact
- 0.00