IMMUNE CONTROL OF WEST NILE VIRUS QUASISPECIES DYNAMICS
IMMUNE CONTROL OF WEST NILE VIRUS QUASISPECIES DYNAMICS
批准号:
8635271
负责人:
James D Brien
金额:
$16.07万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-02-01 至 2018-01-31
关键词:
AddressAmalgamAntibodiesAntiviral AgentsAttenuated Live Virus VaccineBrainC57BL/6 MouseCellsCongenic MiceDataDendritic CellsDengue VirusDevelopmentDiseaseEscape MutantEvolutionFamily memberFibroblastsFlaviviridaeFutureGenerationsGenesGeneticGenetic VariationGenomicsGoalsGrowthHIVHepatitis C virusIFNAR1 geneIRF1 geneIRF3 geneImmuneImmune responseImmune systemImmunocompetenceIn VitroIndividualInfectionInterferon Type IInterferonsLeadLipidsMediatingModelingMonitorMouse StrainsMusMutationNatureNucleotidesOrganPathogenesisPathologyPathway interactionsPopulationProteinsRNA VirusesRNA-Directed RNA PolymeraseResistanceRetroviridaeRoleSafetySerial PassageSerumSeverity of illnessSignal PathwaySignal TransductionSorting - Cell MovementSourceSpleenTranslationsVaccinesVariantViralViral GenomeVirulenceVirusVirus DiseasesWest Nile virusWorkadaptive immunityautocrinecell typedeep sequencingdesigneffective therapygene functionimmunogenicityin vivomRNA Transcript Degradationmacrophagemembernovel strategiesparacrinepressureresearch studyresponsetooltransmission processtype I interferon receptorviral fitnessvirus genetics
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): RNA viruses do not exist in nature as a single genomic sequence, but rather as an amalgam of related sequences referred to as a viral swarm or quasispecies. This proposal is designed to characterize the functional consequences of virus sequence variation within hosts that vary in immunological competence using WNV as a model. This proposal aims to identify how the type I IFN response differentially restricts viral growth an disease caused by a genetically homogenous versus heterogeneous virus population. It also addresses the effect of type I IFN on the evolution of the WNV genome, leading to a better understanding of the viral sequences and diversity (both nucleotide and protein) that are restricted by the type I IFN signaling pathway. A greater understanding of the interactions between type I IFN and a viral swarm could promote novel strategies to limit viral diversity, immune escape, and disease severity. In addition, understanding how type I IFN controls viral evolution could promote increased safety and immunogenicity of live attenuated vaccines, as most vaccines are derived from infectious clones, a source of homogenous virus.
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