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Affinity Purification of Influenza Virus Ribonucleoprotein Complexes from the Chromatin of Infected Cells
Published on: June 3, 2012
Transforming acidic coiled-coil containing protein 3 suppresses influenza A virus replication by impeding viral
Lulu Deng1, Lingcai Zhao1, Jiayu Jin1
1MOE Joint International Research Laboratory of Animal Health and Food Safety, Engineering Laboratory of Animal Immunity of Jiangsu Province, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, China.
Abstract:
Transforming acidic coiled-coil containing protein 3 (TACC3) is a motor spindle protein that plays an essential role in stabilization of the mitotic spindle. In this study, we show that the overexpression of TACC3 reduces the viral titers of multiple influenza A viruses (IAVs). In contrast, the downregulation of TACC3 increases IAVs propagation. Next, we map the target steps of TACC3 requirement to the early stages of viral replication. By confocal microscopy and nuclear plasma separation experiment, we reveal that overexpression of TACC3 results in a substantial decrease of IAV NP accumulation in the nuclei of infected cells. We further show that viral attachment and internalization are not affected by TACC3 overexpression and detect that the early and late endosomal trafficking of IAV in TACC3 overexpression cells is slower than negative control cells. These results suggest that TACC3 exerts an impaired effect on the endosomal trafficking and nuclear import of vRNP, thereby negatively regulating IAV replication. Moreover, the infection of different IAV subtypes decreases the expression level of TACC3 in turn. Consequently, we speculate that IAV ensures the generation of offspring virions by antagonizing the expression of inhibitory factor TACC3. Collectively, our results establish TACC3 as an important inhibitory factor for replication of the IAV, suggesting that TACC3 could be a potential target for the development of future antiviral compounds.
Insights
Transforming acidic coiled-coil containing protein 3 (TACC3) inhibits influenza A virus (IAV) replication by impairing viral endosomal trafficking and nuclear import. IAV infection also reduces TACC3 expression, suggesting a viral counter-strategy.
Area of Science:
- Virology
- Cell Biology
- Molecular Biology
Background:
- Transforming acidic coiled-coil containing protein 3 (TACC3) is crucial for mitotic spindle stability.
- Influenza A viruses (IAVs) are significant human pathogens requiring host factors for replication.
Purpose of the Study:
- To investigate the role of TACC3 in the replication cycle of influenza A viruses.
- To identify specific stages of viral replication affected by TACC3.
Main Methods:
- Overexpression and downregulation of TACC3 in host cells.
- Confocal microscopy and nuclear-plasma separation experiments.
- Analysis of viral attachment, internalization, endosomal trafficking, and nuclear import.
Main Results:
- TACC3 overexpression reduced viral titers and impaired nuclear import of viral components.
- TACC3 downregulation enhanced viral propagation.
- Slower endosomal trafficking of IAV observed in TACC3-overexpressing cells.
- IAV infection decreased TACC3 expression levels.
Conclusions:
- TACC3 acts as a host inhibitory factor against IAV replication.
- TACC3 interferes with viral endosomal trafficking and nuclear import.
- IAV may antagonize TACC3 expression to promote its own replication.
- TACC3 represents a potential therapeutic target for antiviral development.
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