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Crystal structure of spring viremia of carp virus phosphoprotein central domain
Structural highlights
Publication Abstract from PubMedSpring viremia of carp virus (SVCV) is a highly pathogenic Vesiculovirus in the common carp. The phosphoprotein (P protein) of SVCV is a multifunctional protein that acts as a polymerase cofactor and an antagonist of cellular interferon (IFN) response. Here, we report the 1.5-A-resolution crystal structure of the P protein central domain (PCD) of SVCV (SVCVPCD). The PCD monomer consists of two beta sheets, an alpha helix, and another two beta sheets. Two PCD monomers pack together through their hydrophobic surfaces to form a dimer. The mutations of residues on the hydrophobic surfaces of PCD disrupt the dimer formation to different degrees and affect the expression of host IFN consistently. Therefore, the oligomeric state formation of the P protein of SVCV is an important mechanism to negatively regulate host IFN response.IMPORTANCE SVCV can cause spring viremia of carp with up to 90% lethality, and it is the homologous virus of the notorious vesicular stomatitis virus (VSV). There are currently no drugs that effectively cure this disease. P proteins of negative-strand RNA viruses (NSVs) play an essential role in many steps during the replication cycle and an additional role in immunosuppression as a cofactor. All P proteins of NSVs are oligomeric, but the studies on the role of this oligomerization mainly focus on the process of virus transcription or replication, and there are few studies on the role of PCD in immunosuppression. Here, we present the crystal structure of SVCVPCD A new mechanism of immune evasion is clarified by exploring the relationship between SVCVPCD and host IFN response from a structural biology point of view. These findings may provide more accurate target sites for drug design against SVCV and provide new insights into the function of NSVPCD. Structural and Functional Characterization of the Phosphoprotein Central Domain of Spring Viremia of Carp Virus.,Wang ZX, Liu SB, Guan H, Lu LF, Tu JG, Ouyang S, Zhang YA J Virol. 2020 Jul 16;94(15). pii: JVI.00855-20. doi: 10.1128/JVI.00855-20. Print , 2020 Jul 16. PMID:32434890[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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