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A Murine Model of Dengue Virus-induced Acute Viral Encephalitis-like Disease
Published on: April 28, 2019
EXO70 protein influences dengue virus secretion
Zhaoni Chen1, Xing Lin, Zhiwei Zhang
1Department of Pharmacology, Guangxi Medical University, 22 Shuangyong Road, Nanning, Guangxi 530021, PR China.
Microbes and Infection
|November 2, 2010
Summary
Dengue virus (DENV) uses the host protein EXO70 to aid its exit from cells. Reducing EXO70 levels significantly hinders DENV production by affecting virus secretion, not replication.
Area of Science:
- Virology
- Cell Biology
- Molecular Biology
Background:
- The mechanisms by which flaviviruses, like dengue virus (DENV), exit host cells via exocytosis are not fully understood.
- Host cell machinery involvement in viral particle release remains an area of active investigation.
Purpose of the Study:
- To investigate the role of exocyst components, specifically EXO70, in facilitating dengue virus (DENV) exocytosis.
- To determine if DENV utilizes the exocyst complex for efficient virus particle release.
Main Methods:
- Knock-down experiments to reduce EXO70 protein levels in DENV-infected cells.
- Analysis of viral transcription, translation, and secretion.
- Monitoring of EXO70 expression levels post-DENV infection.
- Investigating the influence of DENV proteins (envelope, pre-membrane) on EXO70 expression.
Main Results:
- Knock-down of EXO70 significantly reduced dengue virus production.
- EXO70 primarily affects virus egression/secretion, not viral transcription or translation.
- EXO70 expression is upregulated post-DENV infection, particularly with co-expression of DENV envelope and pre-membrane proteins.
- The pre-membrane protein may facilitate proper folding of the envelope protein, influencing EXO70 upregulation.
Conclusions:
- The host protein EXO70 plays a crucial role in dengue virus exocytosis.
- EXO70 facilitates the secretion of DENV particles from infected cells.
- Upregulation of EXO70 during infection likely supports efficient virus release.
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