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

Author:

King Cason R.1ORCID,Dodge Mackenzie J.2,MacNeil Katelyn M.2,Tessier Tanner M.34,Mymryk Joe S.2567ORCID,Mehle Andrew1ORCID

Affiliation:

1. Department of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, Wisconsin, USA

2. Department of Microbiology and Immunology, University of Western Ontario, London, Ontario, Canada

3. Division of Protective Immunity, The Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania, USA

4. Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA

5. Department of Oncology, University of Western Ontario, London, Ontario, Canada

6. Department of Otolaryngology, University of Western Ontario, London, Ontario, Canada

7. London Regional Cancer Program, Lawson Health Research Institute, London, Ontario, Canada

Abstract

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. IMPORTANCE In 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.

Funder

Life Sciences Research Foundation

Burroughs Wellcome Fund

Wisconsin Alumni Research Foundation

Publisher

American Society for Microbiology

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