Microbiome Core
微生物组核心
基本信息
- 批准号:10579864
- 负责人:
- 金额:$ 15.9万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2019
- 资助国家:美国
- 起止时间:2019-03-05 至 2024-02-29
- 项目状态:已结题
- 来源:
- 关键词:16S ribosomal RNA sequencingAerobicAlgorithmsAntigensBioinformaticsCell physiologyCellsCharacteristicsClinicalCollaborationsComputer AnalysisCustomDataDatabasesDendritic CellsEquilibriumGenesGenomeGoalsHumanImmuneImmune responseImmunityImmunologyInvestigationLaboratoriesLengthLibrariesLiteratureLungLung immune responseLymphocyteMacrophageMediatingMetagenomicsMicrobeMicrofluidicsMiningMolecularMotivationMucous MembraneNasopharynxOralPathway interactionsPatientsPhenotypeProcessResearch PersonnelResearch Project GrantsResolutionSamplingServicesShapesShotgun SequencingSiteSkinSpecificitySpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationSpectroscopy, Fourier Transform InfraredStructure of parenchyma of lungSurfaceSystemTechnologyThe Jackson LaboratoryTissuesValidationVariantViralVirus Diseasescomparative genomicscomputational pipelinescomputer infrastructurecostdysbiosisexperimental studygenome sequencinggut microbiotahuman microbiotaimmune functionimmunoregulationin silicoin vitro Assayinnovationinterestmetagenomemicrobialmicrobial communitymicrobial genomicsmicrobial productsmicrobiomemicrobiome analysismicrobiotanoveloral bacteriaoral microbial communityoverexpressionpathogenpulmonary functionreconstructionresponsereverse geneticsstemtechnology developmentwhole genome
项目摘要
PROJECT SUMMARY MICROBIOME CORE
The microbiome is a critical factor in educating both systemic as well as local immunity. Compartmentalized
immune interactions with the resident flora have been identified at barrier tissues of the body, including the skin,
gut, and lung. Each of these niches has different microbes and microbial community characteristics, which in
turn uniquely shape and maintain innate and adaptive responses. In the lung, host immune responses to
pathogen colonization—whether bacterial, fungal, or viral—are highly influenced by the local microbiota. A
central hypothesis of this center is that the activity and specificity of the lung immune response can be amplified
or diminished based on microbial configurations. Thus, to understand the milieu and activity of tissue-resident
lung cells, including macrophages, lung dendritic cells, and lymphocytes, we must investigate the composition
and functional interactions of the local microbiome with the host tissue.
The central goal of the Microbiome Core is to enable discovery of mechanisms by which the microbiome
influences lung immune function, as per the goals of The Jackson Laboratory Cooperative Center on Human
Immunology (JAX CCHI). The Microbiome Core will be closely integrated with the Sample Core, providing
sequence data, microbial cultivars, and computational analyses for both Research Projects and the Technology
Development project. The Microbiome Core provides unique experimental and computational infrastructures that
are not available as commodity services within or outside of The Jackson Laboratory. Key innovations that the
Core brings to the JAX CCHI include: state-of-the-art metagenomic shotgun sequencing technologies and
analyses at species- and strain-resolution; functional reconstructions; associative analyses with immune
phenotypes; low-cost, microfluidics-based microbial isolate genome extraction; and MALDI (Matrix Assisted
Laser Desorption/Ionization) technology for rapid assessment of strain identity and diversity. The application of
these technologies to the goals of the JAX CCHI will be organized around three Specific Aims:
AIM 1. Reconstruct microbial community composition from clinical samples at high resolution.
AIM 2. Systematic cultivation of microbiota.
AIM 3. Computational prediction of microbiome-immune interactions.
Impact: The Core’s experimental and computational infrastructure will provide both the associative and
mechanistic underpinnings for the CCHI’s central goals of understanding how the microbiome may modulate the
lung’s immune response to viral perturbation.
项目总结微生物组核心
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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Julia S Oh其他文献
Julia S Oh的其他文献
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{{ truncateString('Julia S Oh', 18)}}的其他基金
Developing in situ transcriptomics of a bioprinted follicular skin model
开发生物打印毛囊皮肤模型的原位转录组学
- 批准号:
10678027 - 财政年份:2023
- 资助金额:
$ 15.9万 - 项目类别:
Molecular Mechanisms of Staphylococcus Epidermidis Strain Diversity
表皮葡萄球菌菌株多样性的分子机制
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10539139 - 财政年份:2021
- 资助金额:
$ 15.9万 - 项目类别:
Molecular Mechanisms of Staphylococcus Epidermidis Strain Diversity
表皮葡萄球菌菌株多样性的分子机制
- 批准号:
10412521 - 财政年份:2021
- 资助金额:
$ 15.9万 - 项目类别:
Molecular Mechanisms of Staphylococcus Epidermidis Strain Diversity
表皮葡萄球菌菌株多样性的分子机制
- 批准号:
10328966 - 财政年份:2021
- 资助金额:
$ 15.9万 - 项目类别:
Topological Mapping of Immune, Microbiota, Metabolomic and Clinical Phenotypes to Reveal ME/CFS Disease Mechanisms - Basic Research Project
免疫、微生物群、代谢组学和临床表型的拓扑图绘制以揭示 ME/CFS 疾病机制 - 基础研究项目
- 批准号:
10011904 - 财政年份:2017
- 资助金额:
$ 15.9万 - 项目类别:
Topological Mapping of Immune, Microbiota, Metabolomic and Clinical Phenotypes to Reveal ME/CFS Disease Mechanisms - Basic Research Project
免疫、微生物群、代谢组学和临床表型的拓扑图绘制以揭示 ME/CFS 疾病机制 - 基础研究项目
- 批准号:
10248308 - 财政年份:2017
- 资助金额:
$ 15.9万 - 项目类别:
Topological Mapping of Immune, Microbiota, Metabolomic and Clinical Phenotypes to Reveal ME/CFS Disease Mechanisms - Basic Research Project
免疫、微生物群、代谢组学和临床表型的拓扑图绘制以揭示 ME/CFS 疾病机制 - 基础研究项目
- 批准号:
9769922 - 财政年份:
- 资助金额:
$ 15.9万 - 项目类别:
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