Population dynamic models of microbial interactions
Population dynamic models of microbial interactions
批准号:
10220062
负责人:
CHRISTOPHER HASKELL REMIEN
金额:
$16.35万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2015
资助国家:
美国
项目状态:
未结题
起止时间:
2015-03-15 至 2025-06-30
关键词:
AntibioticsAttentionBiologicalClostridium difficileCommunitiesComplexDataDevelopmentDiseaseEnvironmentEtiologyFoundationsGoalsHealthHealth PromotionHumanHuman MicrobiomeIndividualInfectionIrritable Bowel SyndromeMathematicsMeasuresMediatingMethodologyMethodsMicrobeModelingModernizationOutcomePhasePopulationPopulation DynamicsPopulation GeneticsPropertyResearchResearch PersonnelResistanceResourcesRiskSeriesStatistical MethodsTimeToxinTranslatingWorkalpha Toxinbaseclinically relevantdata analysis pipelinedesignhigh riskinnovationinterestmathematical modelmembermicrobialmicrobial communitymicrobiomemicrobiome researchmicroorganism interactionnovelopportunistic pathogenpathogenrepairedresiliencetheoriestooltraitvaginal microbiome
中文摘要
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英文摘要
The association between human microbiomes and health has garnered a great deal of scientific and popular
attention. By allowing rapid and inexpensive characterization of microbial community composition, modern
sequencing has uncovered enormous microbial diversity. Determining the presence versus absence of microbes
is insufficient however; we need to understand how dysfunctional microbiomes form and how to repair them. A
critical step toward the goal of promoting the assembly of microbial communities that support health is to predict
their temporal dynamics. There remains, however, a critical gap: untangling causation from correlation. Simply
stated, we are currently unable to interpret the biological and clinical relevance buried within the extreme
complexity of microbial communities. Our long-term goal is to advance microbiome research by a) developing
new models that capture causality in microbial interactions; and b) developing tools to interpret the relevance of
microbial interactions for human health. Before the development of data analysis pipelines, we need to establish
theoretical underpinnings upon which to base the methods. We have three aims focused on developing such
theory. (1) Develop molecule-mediated models of microbial interactions. Existing statistical approaches for
modeling the temporal dynamics of microbiomes are built on assumptions that are rarely valid for microbial
communities and thus can be profoundly misleading. Misspecified models may mislead researchers toward poor
prediction of dynamics, or worse, prescription of a misguided treatment that enhances rather than inhibits a
microbial species of interest—a major problem if the species of interest is a pathogen. We will assess the
predictive power of statistical time-series models given realistic molecule-mediated interactions in synthetic data
and develop new statistical methods that account for time-varying interactions. (2) Predict stability of a
microbiome. Even when interactions that govern microbial population dynamics are well estimated, these
interactions may not be directly relevant to human health. Rather, we may want to predict higher-level properties
of a microbiome such as its resilience. Resilience—the ability of a microbiome to maintain and recover function
in the face of perturbations such as by antibiotics or opportunistic pathogens—is related to the mathematical
concept of stability. We will develop new measures to capture the resilience of the microbiome. (3) Predict other
high-level microbiome properties. Often a property of the microbiome in its entirety is of interest, such as the
ability to regulate pH or metabolize a toxin. Borrowing from population genetic theory, we will develop novel
mathematical models to predict the temporal dynamics of traits associated with the microbiome. Together, these
aims will greatly enhance our understanding and interpretation of the temporal dynamics of microbial
communities, and lay the foundation for our capacity to influence their trajectories toward desired outcomes.
This research will provide a critical step in enhancing our ability to assess risk, design synthetic microbial
communities to perform tasks, and manipulate microbiomes to promote health.
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Population dynamic models of microbial interactions
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批准号:10026005
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项目类别:
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资助金额:$16.35万
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财政年份:--
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负责人:CHRISTOPHER HASKELL REMIEN
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依托单位:
国内基金
海外基金
多模态超声VisTran-Attention网络评估早期子宫颈癌保留生育功能手术可行性
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批准号:--
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项目类别:青年科学基金项目
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资助金额:30万元
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批准年份:2022
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负责人:郑巧
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依托单位:
Ultrasomics-Attention孪生网络早期精准评估肝内胆管癌免疫治疗的研究
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批准号:--
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项目类别:面上项目
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资助金额:52万元
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批准年份:2022
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负责人:陈立达
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依托单位: