Key result
Picornavirus 3C protease promotes viral replication and subverts host innate immunity by hijacking host factors, inhibiting interferon production, and modifying host organelles.
Why the study?
This review was conducted to highlight picornavirus-mediated pathogenesis by focusing on the molecular mechanisms through which protease 3C mediates physiological processes in virus-host interaction.
This review summarizes the role of the picornavirus 3C protease in viral replication and subversion of host immune responses.
May inform antiviral targeting of 3C protease; leaves open clinical translation in picornavirus infections.
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.
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Yi et al. (2021) conducted a review in Picornavirus infection. Picornavirus 3C protease was evaluated. Picornavirus 3C protease promotes viral replication and subverts host innate immunity by hijacking host factors, inhibiting interferon production, and modifying host organelles.
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