Shuai Li,Jie Song,Jia Liu,Shijun Zhou,Gaihong Zhao,Tingting Li,Li Huang,Jiangnan Li,Changjiang Weng

J Biol Chem.2024 Apr 22:107307.doi: 10.1016/j.jbc.2024.107307. Online ahead of print.

Abstract

African swine fever (ASF), caused by the African swine fever virus (ASFV), is a viral hemorrhagic disease that affects domestic pigs and wild boars. ASFV infection causes extensive tissue damage, and the associated mechanism is poorly understood. Pyroptosis is characterized by the activation of inflammatory caspases and pore formation in the cellular plasma membrane, resulting in the release of inflammatory cytokines and cell damage. How ASFV infection regulates pyroptosis remains unclear. Here, using small interfering RNA assay and overexpression methods, we report that ASFV infection regulated pyroptosis by cleaving the pyroptosis execution protein gasdermin A (GSDMA). ASFV infection activated caspase-3 and caspase-4, which specifically cleaved GSDMA at D75-P76 and D241-V242 to produce GSDMA into five fragments, including GSDMA-N_1-75, GSDMA-N_1-241, and GSDMA-N76-241 fragments at the N terminal end of GSDMA. Only GSDMA-N1-241, which was produced in the late stage of ASFV infection, triggered pyroptosis and inhibited ASFV replication. The fragments GSDMA-N_1-75 and GSDMA-N_76-241 lose the ability to induce pyroptosis. Overall ASFV infection differentially regulates pyroptosis by GSDMA in the indicated phase, which may be conducive to its own replication. Our findings reveal a novel molecular mechanism for the regulation of pyroptosis.

Keywords: African swine fever; Caspase-3; Caspase-4; GADMA; Pyroptosis.