Replication-Competent Influenza A and B Viruses Expressing a Fluorescent Dynamic Timer Protein for In Vitro and In Vivo Studies

• Published in: PloS one 2016-01, Vol.11 (1), p.e0147723-e0147723
• Main Authors: Breen, Michael, Nogales, Aitor, Baker, Steven F, Perez, Daniel R, Martínez-Sobrido, Luis
• Format: Article
• Language: English
• Subjects: Animals; Biology and life sciences; Breen, Michael; Cell culture; Cytometry; Development and progression; Dogs; Epidemics; Fatalities; Feasibility studies; Flow cytometry; Fluorescence; Genetic aspects; Growth kinetics; Health aspects; HEK293 Cells; Humans; In vivo methods and tests; Infections; Influenza; Influenza A; Influenza A virus - genetics; Influenza A virus - physiology; Influenza B virus - genetics; Influenza B virus - physiology; Influenza viruses; Influenza, Human - genetics; Influenza, Human - metabolism; Kinetics; Life assessment; Luminescent Proteins - genetics; Luminescent Proteins - metabolism; Medicine and health sciences; Microscopy; Orthomyxoviridae; Pandemics; Physical Sciences; Physiological aspects; Plates (structural members); Replication; Research and Analysis Methods; Respiratory diseases; Tissue culture; Viral infections; Virus replication; Virus Replication - genetics; Virus Replication - physiology; Viruses
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0147723

Influenza A and B viruses (IAV and IBV, respectively) cause annual seasonal human respiratory disease epidemics. In addition, IAVs have been implicated in occasional pandemics with inordinate health and economic consequences. Studying influenza viruses in vitro or in vivo requires the use of laborious secondary methodologies to identify infected cells. To circumvent this requirement, replication-competent infectious influenza viruses expressing an easily traceable fluorescent reporter protein can be used. Timer is a fluorescent protein that undergoes a time-dependent color emission conversion from green to red. The rate of spectral change is independent of Timer protein concentration and can be used to chronologically measure the duration of its expression. Here, we describe the generation of replication-competent IAV and IBV where the viral non-structural protein 1 (NS1) was fused to the fluorescent dynamic Timer protein. Timer-expressing IAV and IBV displayed similar plaque phenotypes and growth kinetics to wild-type viruses in tissue culture. Within infected cells, Timer's spectral shift can be used to measure the rate and cell-to-cell spread of infection using fluorescent microscopy, plate readers, or flow cytometry. The progression of Timer-expressing IAV infection was also evaluated in a mouse model, demonstrating the feasibility to characterize IAV cell-to-cell infections in vivo. By providing the ability to chronologically track viral spread, Timer-expressing influenza viruses are an excellent option to evaluate the in vitro and in vivo dynamics of viral infection.