PCV2 Cap protein nuclear import via importin α/β receptor: molecular insights and antiviral potential

Porcine circovirus type 2 (PCV2) Cap protein serves as the primary structural component and plays multiple roles in viral infection. Previous studies have shown that Cap predominantly localizes to the nucleus, but the molecular mechanisms governing its nuclear import remain unclear. This study demonstrates that PCV2 Cap undergoes an active nuclear transport process dependent on Ran-GTP and importin α, but not transportin-1. Co-immunoprecipitation assays revealed interactions between Cap and several host nuclear transport receptors (NTRs), including all importin α subunits, importin 4, 5, 7, and 11. Furthermore, the small molecule inhibitor importazole (IPZ) partially inhibits the nuclear translocation of Cap and suppresses Cap expression, as well as PCV2 replication. While ivermectin (IVM) only impedes transport without affecting viral replication. These findings provide significant insights into the molecular mechanisms of PCV2-Cap nuclear import and highlight potential therapeutic targets for antiviral strategies aimed at disrupting viral capsid transport.

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Publication Details

Journal
Frontiers in Microbiology
Published
2025-11-19
DOI
https://doi.org/10.3389/fmicb.2025.1701697
Primary Topic
Animal Virus Infections Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

PCV2 Cap protein nuclear import via importin α/β receptor: molecular insights and antiviral potential

Cui Lin, Chengcheng Wu, Haiqin Li, Yanbing Zeng et al.
Frontiers in Microbiology
Animal Virus Infections Studies
article

PCV2 Cap protein nuclear import via importin α/β receptor: molecular insights and antiviral potential

Cui Lin, Chengcheng Wu, Haiqin Li, Yanbing Zeng, Fanfan Zhang, Lihan Tao, Na Li, Yi Huang, Jiezhi Ma, Jia Tan, Shu Fang, Xiaofei Zeng
article en

Abstract

Porcine circovirus type 2 (PCV2) Cap protein serves as the primary structural component and plays multiple roles in viral infection. Previous studies have shown that Cap predominantly localizes to the nucleus, but the molecular mechanisms governing its nuclear import remain unclear. This study demonstrates that PCV2 Cap undergoes an active nuclear transport process dependent on Ran-GTP and importin α, but not transportin-1. Co-immunoprecipitation assays revealed interactions between Cap and several host nuclear transport receptors (NTRs), including all importin α subunits, importin 4, 5, 7, and 11. Furthermore, the small molecule inhibitor importazole (IPZ) partially inhibits the nuclear translocation of Cap and suppresses Cap expression, as well as PCV2 replication. While ivermectin (IVM) only impedes transport without affecting viral replication. These findings provide significant insights into the molecular mechanisms of PCV2-Cap nuclear import and highlight potential therapeutic targets for antiviral strategies aimed at disrupting viral capsid transport.

Frontiers in MicrobiologyVol. 16
Jiangxi University of Technology (CN), Animal Science Research Institute (CN), Nanchang Center for Disease Control and Prevention (CN), Jiangxi Academy of Agricultural Sciences (CN), Jiangxi Agricultural University (CN)
National Natural Science Foundation of China, Jiangxi Academy of Agricultural Sciences
Openalex Percentile: Top 59%
Animal Virus Infections Studies
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PCV2 Cap protein nuclear import via importin α/β receptor: molecular insights and antiviral potential — Cui Lin, Chengcheng Wu, et al. · Frontiers in Microbiology (2025) | TGRS Research Map | TGRS