Expanding the adenovirus toolbox: reporter viruses for studying the dynamics of human adenovirus replication

J Virol. 2024 May 14;98(5):e0020724. doi: 10.1128/jvi.00207-24. Epub 2024 Apr 19.

Abstract

To streamline standard virological assays, we developed a suite of nine fluorescent or bioluminescent replication competent human species C5 adenovirus reporter viruses that mimic their parental wild-type counterpart. These reporter viruses provide a rapid and quantitative readout of various aspects of viral infection and replication based on EGFP, mCherry, or NanoLuc measurement. Moreover, they permit real-time non-invasive measures of viral load, replication dynamics, and infection kinetics over the entire course of infection, allowing measurements that were not previously possible. This suite of replication competent reporter viruses increases the ease, speed, and adaptability of standard assays and has the potential to accelerate multiple areas of human adenovirus research.IMPORTANCEIn this work, we developed a versatile toolbox of nine HAdV-C5 reporter viruses and validated their functions in cell culture. These reporter viruses provide a rapid and quantitative readout of various aspects of viral infection and replication based on EGFP, mCherry, or NanoLuc measurement. The utility of these reporter viruses could also be extended for use in 3D cell culture, organoids, live cell imaging, or animal models, and provides a conceptual framework for the development of new reporter viruses representing other clinically relevant HAdV species.

Keywords: NanoLuc; adenovirus; bioluminescence; fluorescence; gene expression; microneutralization assay; plaque assay; reporter virus; viral kinetics; viral replication compartments.

MeSH terms

  • Adenovirus Infections, Human / virology
  • Adenoviruses, Human* / genetics
  • Adenoviruses, Human* / physiology
  • Cell Line
  • Genes, Reporter*
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • HEK293 Cells
  • Humans
  • Viral Load
  • Virus Replication*