6533b86efe1ef96bd12cb5cf

RESEARCH PRODUCT

Social evolution of innate immunity evasion in a virus

Rafael SanjuánMaria Duran-morenoPilar Domingo-calapErnesto Segredo-otero

subject

Microbiology (medical)virusesImmunologyBiologyApplied Microbiology and BiotechnologyMicrobiologyAntiviral AgentsModels BiologicalArticleVirusVesicular stomatitis Indiana virus03 medical and health sciencesMiceViral ProteinsInterferonImmunityGeneticsmedicineAnimals030304 developmental biologyImmune Evasion0303 health sciencesMice Inbred BALB CInnate immune systemNatural selection030306 microbiologyBrainCell BiologyDNA-Directed RNA Polymerasesbiology.organism_classificationAltruismVirologyBiological EvolutionImmunity Innate3. Good healthDisease Models AnimalVesicular stomatitis virusViral evolutionHost-Pathogen InteractionsFemaleInterferonsSocial evolutionmedicine.drug

description

Antiviral immunity has been studied extensively from the perspective of virus−cell interactions, yet the role of virus−virus interactions remains poorly addressed. Here, we demonstrate that viral escape from interferon (IFN)-based innate immunity is a social process in which IFN-stimulating viruses determine the fitness of neighbouring viruses. We propose a general and simple social evolution framework to analyse how natural selection acts on IFN shutdown and validate it in cell cultures and mice infected with vesicular stomatitis virus. Furthermore, we find that IFN shutdown is costly because it reduces short-term viral progeny production, thus fulfilling the definition of an altruistic trait. Hence, in well-mixed populations, the IFN-blocking wild-type virus is susceptible to invasion by IFN-stimulating variants and spatial structure consequently determines whether IFN shutdown can evolve. Our findings reveal that fundamental social evolution rules govern viral innate immunity evasion and virulence and suggest possible antiviral interventions.

10.1038/s41564-019-0379-8http://dx.doi.org/10.1038/s41564-019-0379-8