Salmonid alphavirus non-structural protein 2 is a key protein that activates the NF-KB signaling pathway to mediate inflammatory responses

Salmonid alphavirus (SAV) infection of Atlantic salmon (Salmo salar) and rainbow trout (Oncorhynchus mykiss) causes pancreas disease (PD) with typical inflammatory responses, such as necrosis of the exocrine pancreas, cardiomyopathy and skeletal myopathy. However, the pathogenic mechanism underlying SAV infection is still unclear. Inflammation may cause damage to the body, but it is a defense response against infection by pathogenic microorganisms, of which nuclear factor-kappa B (NF-KB) is the main regulator. This study revealed that SAV can activate NF-KB, of which the viral nonstructural protein Nsp2 is the major activating protein. SAV activates the NF-KB signaling pathway by simultaneously up-regulating TLR3, 7, 8 and then the expression of the signaling molecule myeloid differentiation factor 88 (Myd88) and tumor necrosis factor receptor-associated factor 6 (TRAF6). We found that Nsp2 can induce IKB degradation and p65 phosphorylation and transnucleation, and activate NF-KB downstream inflammatory cytokines. Nsp2 may simultaneously activate NF-KB through TLR3,7,8-dependent signaling pathways. Overexpression of Nsp2 can up-regulate mitochondrial antiviral signaling protein (MAVS) and then promote the expression of IFNa1 and antiviral protein Mx, which inhibits viral replication. This study shows that Nsp2 acts as a key activator protein for the NF-KB signaling pathway, which induces inflam-mation post-SAV infection. This study systematically analyzes the molecular mechanism of SAV activation of the NF-KB signaling pathway, and provides a theoretical basis for revealing the mechanism of innate immune response and inflammatory injury caused by SAV.

Automated summary

This study reveals that Salmonid alphavirus infection activates the NF-KB signaling pathway and induces inflammation. The viral nonstructural protein Nsp2 is identified as the major activator of NF-KB, promoting immune cell signaling and antiviral response to inhibit viral replication.