A Fluorescent Reporter Virus Toolkit for Interrogating Enterovirus Biology and Host Interactions
Mireya Martínez-Pérez,
Sebastian Velandia-Álvarez,
Cristina Vidal-Verdú,
Beatriz Álvarez-Rodríguez,
Ron Geller
Affiliations
Mireya Martínez-Pérez
Institute for Integrative Systems Biology (I<sup>2</sup>SysBio), Universitat de València—Consejo Superior de Investigaciones Científicas (UV-CSIC), 46980 Valencia, Spain
Sebastian Velandia-Álvarez
Institute for Integrative Systems Biology (I<sup>2</sup>SysBio), Universitat de València—Consejo Superior de Investigaciones Científicas (UV-CSIC), 46980 Valencia, Spain
Cristina Vidal-Verdú
Institute for Integrative Systems Biology (I<sup>2</sup>SysBio), Universitat de València—Consejo Superior de Investigaciones Científicas (UV-CSIC), 46980 Valencia, Spain
Beatriz Álvarez-Rodríguez
Institute for Integrative Systems Biology (I<sup>2</sup>SysBio), Universitat de València—Consejo Superior de Investigaciones Científicas (UV-CSIC), 46980 Valencia, Spain
Ron Geller
Institute for Integrative Systems Biology (I<sup>2</sup>SysBio), Universitat de València—Consejo Superior de Investigaciones Científicas (UV-CSIC), 46980 Valencia, Spain
Enteroviruses are a group of highly prevalent human pathogens responsible for a wide range of illnesses, ranging from common cold symptoms to life-threatening diseases. A deep understanding of enterovirus biology, evolution, and host interaction is required for the development of effective vaccines and antivirals. Recombinant reporter viruses encoding luminescent or fluorescent proteins have been developed to facilitate such investigation. In this work, using coxsackievirus B3 as our model, we analyze how the insertion of fluorescent reporter genes at three distinct sites within the viral polyprotein affects viral fitness, identifying the most tolerant site for reporter insertion. We then describe a set of experimental workflows for measuring viral fitness, sera neutralization, antiviral efficacy, and recombination using fluorescent reporter viruses. The high homology between different enteroviruses suggests these assays can be readily adapted to study additional members of this medically and economically relevant group of viruses.