| Literature DB >> 32696397 |
Zhaohua Zhong1, Wenran Zhao2, Xiaoman Wo3, Yuan Yuan3, Yong Xu3, Yang Chen4, Yao Wang3, Shuoxuan Zhao3, Lexun Lin4, Xiaoyan Zhong4, Yan Wang4.
Abstract
Enterovirus A71 (EV-A71) is one of the etiological pathogens leading to hand, foot, and mouth disease (HFMD), which can cause severe neurological complications. The neuropathogenesis of EV-A71 infection is not well understood. The mislocalization and aggregation of TAR DNA-binding protein 43 (TDP-43) is the pathological hallmark of amyotrophic lateral sclerosis (ALS). However, whether TDP-43 was impacted by EV-A71 infection is unknown. This study demonstrated that TDP-43 was cleaved during EV-A71 infection. The cleavage of TDP-43 requires EV-A71 replication rather than the activated caspases due to viral infection. TDP-43 is cleaved by viral protease 3C between the residues 331Q and 332S, while mutated TDP-43 (Q331A) was not cleaved. In addition, mutated 3C which lacks the protease activity failed to induce TDP-43 cleavage. We also found that TDP-43 was translocated from the nucleus to the cytoplasm, and the mislocalization of TDP-43 was induced by viral protease 2A rather than 3C. Taken together, we demonstrated that TDP-43 was cleaved by viral protease and translocated to the cytoplasm during EV-A71 infection, implicating the possible involvement of TDP-43 in the pathogenesis of EV-A71infection.Entities:
Keywords: 2A protease; 3C protease; Enterovirus A71 (EV-A71); TAR DNA-binding protein 43 (TDP-43)
Year: 2020 PMID: 32696397 PMCID: PMC7973337 DOI: 10.1007/s12250-020-00262-x
Source DB: PubMed Journal: Virol Sin ISSN: 1995-820X Impact factor: 4.327