7VWV

The crystal structure of African swine fever virus I73R

Summary for 7VWV

• Entry DOI: 10.2210/pdb7vwv/pdb
• Descriptor: I73R (2 entities in total)
• Functional Keywords: asfv, i73r, viral protein
• Biological source: African swine fever virus
• Total number of polymer chains: 2
• Total formula weight: 19424.51

Authors

Shen, Z.,Liang, R. (deposition date: 2021-11-11, release date: 2022-11-16, Last modification date: 2024-05-29)

Primary citation

Liu, Y.,Shen, Z.,Xie, Z.,Song, Y.,Li, Y.,Liang, R.,Gong, L.,Di, D.,Liu, J.,Liu, J.,Chen, Z.,Yu, W.,Lv, L.,Zhong, Q.,Liao, X.,Tian, C.,Wang, R.,Song, Q.,Wang, H.,Peng, G.,Chen, H.
African swine fever virus I73R is a critical virulence-related gene: A potential target for attenuation.
Proc.Natl.Acad.Sci.USA, 120:e2210808120-e2210808120, 2023

PubMed Abstract: African swine fever virus (ASFV) is a large, double-stranded DNA virus that causes a fatal disease in pigs, posing a threat to the global pig industry. Whereas some ASFV proteins have been found to play important roles in ASFV-host interaction, the functional roles of many proteins are still largely unknown. In this study, we identified , an early viral gene in the replication cycle of ASFV, as a key virulence factor. Our findings demonstrate that pI73R suppresses the host innate immune response by broadly inhibiting the synthesis of host proteins, including antiviral proteins. Crystallization and structural characterization results suggest that pI73R is a nucleic-acid-binding protein containing a Zα domain. It localizes in the nucleus and inhibits host protein synthesis by suppressing the nuclear export of cellular messenger RNA (mRNAs). While pI73R promotes viral replication, the deletion of the gene showed that it is a nonessential gene for virus replication. In vivo safety and immunogenicity evaluation results demonstrate that the deletion mutant ASFV-GZΔ is completely nonpathogenic and provides effective protection to pigs against wild-type ASFV. These results reveal as a virulence-related gene critical for ASFV pathogenesis and suggest that it is a potential target for virus attenuation. Accordingly, the deletion mutant ASFV-GZΔ can be a potent live-attenuated vaccine candidate.

PubMed: 37023125
DOI: 10.1073/pnas.2210808120

Experimental method

X-RAY DIFFRACTION (2.59 Å)