» Articles » PMID: 34113334

Nucleolar Phosphoprotein NPM1 Interacts With Porcine Circovirus Type 3 Cap Protein and Facilitates Viral Replication

Overview
Journal Front Microbiol
Specialty Microbiology
Date 2021 Jun 11
PMID 34113334
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Porcine circovirus type 3 (PCV3) is a recently discovered virus with potentially significant implications on the global swine industry. PCV3 replication involves the entry of the viral capsid (Cap) protein with nucleolar localization signals into the nucleus. Using liquid chromatography-mass spectrometry analysis, nucleolar phosphoprotein NPM1 was identified as one of the cellular proteins bound to PCV3 Cap. Co-immunoprecipitation demonstrated that PCV3 Cap interacts directly with NPM1, where the region binding with NPM1 is mapped to amino acid residues 1-38 of Cap. Upon co-transfection, the expression of Cap protein promoted the redistribution of NPM1, which translocated from the nucleus to the cytoplasm and colocalized with Cap in cultured PK15 cells. NPM1 expression was upregulated and translocated from the nucleus to the cytoplasm in PCV3-infected cells, upon siRNA-mediated depletion, or upon treatment with NPM1 inhibitor in PK15 cells with impaired PCV3 replication, as evidenced by decreased levels of viral DNA synthesis and protein expression. By contrast, the replication of PCV3 was enhanced in stably NPM1-expressing cells via a lentivirus-delivered system. Taken together, these findings indicate that NPM1 interacts with PCV3 Cap and plays a crucial role in PCV3 replication.

Citing Articles

DDX21 Promotes PCV3 Replication by Binding to Cap Protein and Inhibiting Interferon Responses.

Sun H, Dai Q, Zhou B, Lan X, Qiu Y, Zhang Q Viruses. 2025; 17(2).

PMID: 40006921 PMC: 11861039. DOI: 10.3390/v17020166.


E3 ligase RNF2 inhibits porcine circovirus type 3 replication by targeting its capsid protein for ubiquitination-dependent degradation.

Wang D, Zhao J, Yang X, Ji Y, Yu J, Li Z J Virol. 2024; 98(8):e0022324.

PMID: 39046246 PMC: 11334428. DOI: 10.1128/jvi.00223-24.


Ubiquitination-dependent degradation of nucleolin mediated by porcine circovirus type 3 capsid protein.

Wang D, Hou L, Ji Y, Xie J, Zhao J, Zhu N J Virol. 2023; 97(12):e0089423.

PMID: 38032196 PMC: 10734473. DOI: 10.1128/jvi.00894-23.


Revisiting Porcine Circovirus Infection: Recent Insights and Its Significance in the Piggery Sector.

Maity H, Samanta K, Deb R, Gupta V Vaccines (Basel). 2023; 11(8).

PMID: 37631876 PMC: 10457769. DOI: 10.3390/vaccines11081308.


Mechanisms of circovirus immunosuppression and pathogenesis with a focus on porcine circovirus 2: a review.

Feher E, Jakab F, Banyai K Vet Q. 2023; 43(1):1-18.

PMID: 37431709 PMC: 10367577. DOI: 10.1080/01652176.2023.2234430.


References
1.
Shi D, Shi H, Sun D, Chen J, Zhang X, Wang X . Nucleocapsid Interacts with NPM1 and Protects it from Proteolytic Cleavage, Enhancing Cell Survival, and is Involved in PEDV Growth. Sci Rep. 2017; 7:39700. PMC: 5206633. DOI: 10.1038/srep39700. View

2.
Day P, Thompson C, Pang Y, Lowy D, Schiller J . Involvement of Nucleophosmin (NPM1/B23) in Assembly of Infectious HPV16 Capsids. Papillomavirus Res. 2016; 1:74-89. PMC: 4934132. DOI: 10.1016/j.pvr.2015.06.005. View

3.
Breitbart M, Delwart E, Rosario K, Segales J, Varsani A, Ictv Report Consortium . ICTV Virus Taxonomy Profile: Circoviridae. J Gen Virol. 2017; 98(8):1997-1998. PMC: 5656780. DOI: 10.1099/jgv.0.000871. View

4.
Colombo E, Alcalay M, Pelicci P . Nucleophosmin and its complex network: a possible therapeutic target in hematological diseases. Oncogene. 2011; 30(23):2595-609. DOI: 10.1038/onc.2010.646. View

5.
Li Y . Protein B23 is an important human factor for the nucleolar localization of the human immunodeficiency virus protein Tat. J Virol. 1997; 71(5):4098-102. PMC: 191564. DOI: 10.1128/JVI.71.5.4098-4102.1997. View