Replication-competent adenovirus reporters utilizing endogenous viral expression architecture

This research provides powerful new tools to rapidly study adenovirus gene expression and replication. By integrating fluorescent and secreted luciferase reporters into native viral regulatory elements, we enable real-time, non-destructive tracking of early and late stage infection in living cells. These modular reporters are compatible with a wide range of genetic and chemical perturbations, allowing researchers to investigate the function of specific viral genes, host interactions, and the impact of host genes and antiviral compounds. Importantly, the high-throughput nature of these systems overcomes limitations of traditional plaque assays to quantify viral replication dynamics. Our work will allow for the rapid creation of both novel infectious and replication-incompetent viral vectors.

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Publication Details

Journal
Journal of Virology
Published
2025-09-10
DOI
https://doi.org/10.1128/jvi.01146-25
Citations
1
Primary Topic
Virus-based gene therapy research
Type
article
Field-Weighted Citation Impact
1.82
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Replication-competent adenovirus reporters utilizing endogenous viral expression architecture

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Replication-competent adenovirus reporters utilizing endogenous viral expression architecture

Molly R. Patterson, Lorenzo Serra, Alexander M. Price, Daniel T. Claiborne, Alison Yu, Colm J. O'Brien, Reyes Acosta
article en
1 citations

Abstract

This research provides powerful new tools to rapidly study adenovirus gene expression and replication. By integrating fluorescent and secreted luciferase reporters into native viral regulatory elements, we enable real-time, non-destructive tracking of early and late stage infection in living cells. These modular reporters are compatible with a wide range of genetic and chemical perturbations, allowing researchers to investigate the function of specific viral genes, host interactions, and the impact of host genes and antiviral compounds. Importantly, the high-throughput nature of these systems overcomes limitations of traditional plaque assays to quantify viral replication dynamics. Our work will allow for the rapid creation of both novel infectious and replication-incompetent viral vectors.

Journal of VirologyVol. 99(10)
The Wistar Institute (US), GNA University (IN), Genome Institute of Singapore (SG), University of Pennsylvania (US), University of Bologna (IT)
Openalex Percentile: Top 13%
Virus-based gene therapy research
1.82
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