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Transgene Expression in Cultured Cells Using Unpurified Recombinant Adeno-Associated Viral Vectors
Published on: October 20, 2023
Effects of adeno-associated virus on adenovirus replication and gene expression during coinfection
Jennifer M Timpe1, Kristin C Verrill, James P Trempe
1Department of Biochemistry and Cancer Biology, Medical University of Ohio, 3035 Arlington Ave., Toledo, OH 43614-5804, USA.
Abstract:
Adeno-associated virus (AAV) is a nonpathogenic parvovirus that requires adenovirus (Ad) or another helper virus for a fully permissive infection. AAV-mediated inhibition of Ad is well documented, yet many details of this interaction remain unclear. In this study, we observed a maximum 50-fold decrease in infectious virus production and a 10- to 40-fold reduction in Ad DNA synthesis during coinfections with AAV. With the exception of the E3 gene, AAV decreased all steady-state Ad mRNA levels at 24 h postinfection (hpi) in a dose-dependent manner. However, not all transcription units were affected equally. E4 and late transcription were the most strongly inhibited, and E1A and E2A were the least affected. The temporal effects of AAV on Ad mRNA transcript levels also varied among the Ad genes. Ad protein expression paralleled mRNA levels at 24 hpi, suggesting that coinfecting AAV does not exert substantial effects on translation. In plasmid transfection assays, Rep78 protein most effectively limited Ad amplification, while Rep40 had no effect. Since E2a and E4 proteins are essential for efficient Ad DNA amplification, we examined the relationship between reduced E2A and E4 expression and decreased DNA amplification. Transfected Rep78 did not reduce E2A and E4 transcript levels prior to DNA replication. Also, AAV-induced inhibition of E2A and E4 mRNA production did not occur in the presence of hydroxyurea. It is therefore unlikely that decreased early gene expression is solely responsible for AAV's suppression of Ad DNA replication. Our results suggest that AAV amplification and/or Rep gene expression inhibits Ad DNA synthesis.
Insights
Adeno-associated virus (AAV) coinfection significantly reduces adenovirus (Ad) production and DNA synthesis. AAV Rep gene expression, not early gene suppression, appears to be the primary mechanism inhibiting Ad replication.
Area of Science:
- Virology
- Molecular Biology
Background:
- Adeno-associated virus (AAV) requires helper viruses like adenovirus (Ad) for replication.
- AAV's inhibitory effects on Ad are known but not fully understood.
Purpose of the Study:
- To investigate the mechanisms by which AAV inhibits Ad replication.
- To determine the role of AAV gene expression in suppressing Ad DNA synthesis.
Main Methods:
- Coinfection of cells with AAV and Ad.
- Analysis of Ad DNA synthesis and mRNA levels.
- Plasmid transfection assays using AAV Rep proteins.
Main Results:
- AAV reduced infectious Ad production by up to 50-fold and Ad DNA synthesis by 10- to 40-fold.
- AAV dose-dependently decreased most Ad mRNA levels, with E4 and late transcripts most affected.
- AAV Rep78 protein inhibited Ad amplification, but not by reducing E2A or E4 transcript levels before DNA replication.
Conclusions:
- AAV inhibits Ad DNA replication through mechanisms independent of early gene expression suppression.
- AAV amplification and/or Rep gene expression are likely responsible for inhibiting Ad DNA synthesis.
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