Picornavirus 3C – a protease ensuring virus replication and subverting host responses

Author:

Yi Jiamin1,Peng Jiangling1,Yang Wenping1,Zhu Guoqiang1,Ren Jingjing1,Li Dan1ORCID,Zheng Haixue1ORCID

Affiliation:

1. State Key Laboratory of Veterinary Etiological Biology and OIE/National Foot and Mouth Disease Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, Gansu730046, China

Abstract

ABSTRACT The protease 3C is encoded by all known picornaviruses, and the structural features related to its protease and RNA-binding activities are conserved; these contribute to the cleavage of viral polyproteins and the assembly of the viral RNA replication complex during virus replication. Furthermore, 3C performs functions in the host cell through its interaction with host proteins. For instance, 3C has been shown to selectively ‘hijack’ host factors involved in gene expression, promoting picornavirus replication, and to inactivate key factors in innate immunity signaling pathways, inhibiting the production of interferon and inflammatory cytokines. Importantly, 3C maintains virus infection by subtly subverting host cell death and modifying critical molecules in host organelles. This Review focuses on the molecular mechanisms through which 3C mediates physiological processes involved in virus–host interaction, thus highlighting the picornavirus-mediated pathogenesis caused by 3C.

Funder

National Natural Science Foundation of China

Chinese Academy of Agricultural Sciences

Publisher

The Company of Biologists

Subject

Cell Biology

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