Abstract

Superinfection exclusion (SIE) is a process by which a virally infected cell is protected from subsequent infection by the same or a closely related virus. By preventing cell coinfection, SIE favors preservation of genome integrity of a viral strain and limits its recombination potential with other viral genomes, thereby impacting viral evolution. Although described in virtually all viral families, the precise step(s) impacted by SIE during the viral life cycle have not been systematically explored. Here, we describe for the first time SIE triggered by chikungunya virus (CHIKV), an alphavirus of public health importance. Using single-cell technologies, we demonstrate that CHIKV excludes subsequent infection with: CHIKV; Sindbis virus, a related alphavirus; and influenza A, an unrelated RNA virus. We further demonstrate that SIE does not depend on the action of type I interferon, nor does it rely on host cell transcription. Moreover, exclusion is not mediated by the action of a single CHIKV protein; in particular, we observed no role for non-structural protein 2 (nsP2), making CHIKV unique among characterized alphaviruses. By stepping through the viral life cycle, we show that CHIKV exclusion occurs at the level of replication, but does not directly influence virus binding, nor viral structural protein translation. In sum, we characterized co-infection during CHIKV replication, which likely influences the rate of viral diversification and evolution.

Highlights

  • RNA viruses achieve genome diversification through a fast mutation rate and a propensity for recombination between different genomes

  • Chikungunya virus superinfection exclusion is broad and not restricted to alphaviruses To study Superinfection exclusion (SIE) triggered by chikungunya virus (CHIKV), we used two reporter viruses derived from an Indian Ocean CHIKV strain: one coding for GFP, inserted immediately after the subgenomic

  • We found that RNA replication was impacted in an multiplicity of infection (MOI)-dependent manner (Fig 7E), reflecting the expression of protein data obtained by flow cytometry (Fig 7F), and indicating that CHIKV SIE acts by inhibiting challenge virus replication

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Summary

Introduction

RNA viruses achieve genome diversification through a fast mutation rate and a propensity for recombination between different genomes. This latter phenomenon necessitates the infection of a cell by at least two genomes and is dependent on the potential for cellular coinfection. In this context, superinfection exclusion (SIE, termed homologous interference), a mechanism by which the infection by a first virus inhibits the infection of a second, typically related, virus, is relevant to genome diversification and virus evolution. Insitro provided support in the form of salaries for M.L.A. The specific roles of these authors are articulated in the ‘author contributions’ section. None of the funders had a role in study design, data collection and analysis, decision to publish, or preparation of the manuscript

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