Foot-and-Mouth Disease Virus Evades Innate Immune Response by 3C-Targeting of MDA5

Foot-and-mouth disease (FMD) is a highly contagious disease caused by FMD virus (FMDV) in cloven-hoofed animals. Retinoic acid-inducible gene I (RIG-I) and melanoma differentiation-associated gene 5 (MDA5) are representative receptors in the cytoplasm for the detection of viral RNA and trigger antiviral responses, leading to the production of type I interferon. Although MDA5 is a crucial receptor for sensing picornavirus RNA, the interplay between MDA5 and FMDV is relatively unknown compared to the interplay between RIG-I and FMDV. Here, we observed that the FMDV infection inhibits MDA5 protein expression. Of the non-structural proteins, the Lb and 3C proteinases (Lb(pro) and 3C(pro)) were identified to be primarily responsible for this inhibition. However, the inhibition by 3C(pro) was independent of proteasome, lysosome and caspase-dependent pathway and was by 3C protease activity. A direct interaction between 3C(pro) and MDA5 protein was observed. In conclusion, this is the first report that 3C(pro) inhibits MDA5 protein expression as a mechanism to evade the innate immune response during FMDV infection. These results elucidate the pathogenesis of FMDV and provide fundamental insights for the development of a novel vaccine or therapeutic agent.

Automated summary

During foot-and-mouth disease virus (FMDV) infection, inhibition of MDA5 protein expression is primarily caused by the non-structural proteins Lb(pro) and 3C(pro), with 3C(pro) directly interacting with MDA5 protein through its protease activity. This study sheds light on the pathogenesis of FMDV and may contribute to the development of novel vaccines or therapeutic agents.