Quantitative studies of influenza evolution
流感进化的定量研究
基本信息
- 批准号:8615424
- 负责人:
- 金额:$ 51.64万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2014
- 资助国家:美国
- 起止时间:2014-02-01 至 2018-12-31
- 项目状态:已结题
- 来源:
- 关键词:AffectAnimal ModelAntibody ActivationAttentionAvian InfluenzaAvian Influenza A VirusBindingBiologyBiomedical ComputingBirdsCell CommunicationCellsCessation of lifeCollaborationsComplexCoupledCytotoxic T-LymphocytesDataDissectionEvolutionFosteringGeneticGenomicsHigh-Throughput RNA SequencingHumanImmune responseImmune systemIn VitroIndividualInfectionInfluenzaInterferon Type ILaboratoriesLeadLife Cycle StagesLivestockMethodsMissionModelingMonitorMutationPatternPhasePhenotypePopulationPopulation DynamicsPopulation StudyProcessProductionPublic HealthRNAResearch InfrastructureResearch PersonnelRiskShapesSourceStructureSystemSystems BiologyTechnologyUniversitiesViralViral GenomeVirusVirus DiseasesWorld Health OrganizationZoonosesbasecomplex biological systemscomputer frameworkfitnessgain of functionin vitro Modelin vivo Modelinfluenza epidemicinfluenza virus vaccineinfluenzavirusinsightmathematical modelmembernovelpandemic diseasepandemic influenzapressureprotein protein interactionpublic health relevanceresearch studyseasonal influenzasegregationsurveillance datatool
项目摘要
An enormous mutation rate, coupled with reassortment (a process analogous to chromosomal segregation) of
RNA segments of the viral genome, and natural zoonosis, have lead to influenza epidemics and pandemics in
humans. It has been estimated seasonal influenza causes approximately 5 million cases annually, resulting in
250,000 to 500,000 deaths. Deaths resulting from pandemic influenza can reach millions and
each year, the
World Health Organization predicts which strains of the virus are most likely to be circulating in the following
year. This approach relies on yearly global surveillance data to monitor ongoing infections in humans and
livestock and is prone to significant error.
A major shortcoming of these data is that they represent a partial
landscape of circulating viruses due to limitations in surveillance and the selective pressures are generated in
an uncontrolled setting making it difficult to assess the affect of complex evolutionary processes.
However,
even when such predictions are accurate, a particular influenza vaccine usually confers protection for no more
We propose to overcome these limitations by
integrating the experimental expertise of the Shapira and Garcia-Sastre laboratories together with
than a few years due to the high mutation rate of the virus.
mathematical modeling and computational framework of the Rabadan laboratory, a member of the Center for
the Multiscale Analysis of Genomic and Cellular Networks (MAGNet; which provides a core framework for
applying systems biology approaches to studying complex biological systems such as influenza evolution).
While it is well established that reassortment between influenza isolates from different host species can
generate viruses with pandemic potential, the relationship between reassortment, viral mutation rates, as well
as the selective pressures imposed on this virus remain key questions in influenza biology and are major issues
for global public health.
Not only does
influenza represent an ideal laboratory model for quantitative studies
of evolution, In
collaboration with MAGNet, we propose to use modern genomic approaches, coupled with genetically
tractable mammalian systems, to determine, in an unprecedented fashion, precisely what evolutionary
changes the virus undergoes as it adapts across species, or as it interacts with the host innate and adaptive
immune systems, to compute the evolutionary trajectory of individual viral sequences, and to identify
selection pressures exerted on the virus. We expect that the experimental and computational platform
described in this proposal will foster new insights into the evolutionary constrains that govern viral evolution.
Coupled with ongoing surveillance efforts, even modest improvements on the current understanding of the
influenza fitness landscape will allow for better assessment of pandemic risk potential of circulating strains.
understanding the variables that influence antigenic drift, and viral adaptation is paramount.
巨大的突变率,加上重组(类似于染色体分离的过程)
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Sagi Shapira其他文献
Sagi Shapira的其他文献
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{{ truncateString('Sagi Shapira', 18)}}的其他基金
Leveraging experimental and computational tools to define molecular functions of non-coding RNAs in innate immune responses to viral infection
利用实验和计算工具来定义非编码RNA在病毒感染先天免疫反应中的分子功能
- 批准号:
10005115 - 财政年份:2019
- 资助金额:
$ 51.64万 - 项目类别:
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