Project 3: Functional Microbiome and Host Signatures in Transition from Commensal to pathogen
Project 3: Functional Microbiome and Host Signatures in Transition from Commensal to pathogen
批准号:
10614695
负责人:
Tor C. Savidge
金额:
$65.13万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
未结题
起止时间:
2020-08-01 至 2026-07-31
关键词:
AchievementAddressAdultAlgorithmsAntibiotic TherapyAntibioticsAntimicrobial ResistanceBacteriaCenters for Disease Control and Prevention (U.S.)Cessation of lifeChildClinicalClinical ManagementClostridium difficileCommunicable DiseasesCommunitiesCritical IllnessDataDevelopmentDiseaseDisease OutcomeDisease ProgressionDisease susceptibilityExtended-spectrum β-lactamaseGoalsHealthcareImmune responseImmunocompromised HostIndigenousIndividualInfantInfectionIntensive Care UnitsLinkMedicalMetabolicMetabolic PathwayMetagenomicsModern MedicineNosocomial InfectionsOrganismOutcomePatientsPhysiciansPopulationPredispositionPublic HealthPublishingResistanceRiskRisk FactorsShotgunsSignal TransductionStem cell transplantStructureSystemTechnologyTestingTherapeutic InterventionTransplant RecipientsVancomycin resistant enterococcusVirulenceantimicrobialbacteriocinbasecarbapenem resistancecohortcombatdesigneffective therapyfunctional genomicsgut colonizationgut microbiotahazardhigh riskhost microbiotaimmunosuppressedinfection managementinfection riskinfectious disease modelinnovationinsightmetaproteomicsmicrobiomemicrobiotamulti-drug resistant pathogennovel strategiesnovel therapeuticspathogenpathogenic bacteriapreventpriority pathogenprospectiveresistant Klebsiella pneumoniaetraittreatment planning
中文摘要
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英文摘要
ABSTRACT
Project 3: Functional Microbiome and Host Signatures in Transition from Commensal to pathogen
Overuse of antibiotics and adaptability of bacteria has resulted in antimicrobial resistance (AMR) in pathogens
of significant public health concern. Identifying individuals who are susceptible to infection is critical in
implementing an effective treatment plan and in promoting good antimicrobial stewardship. This project focuses
on developing innovative systems technology to develop microbiome-based risk algorithms that identify
susceptible patients in the general hospitalized population. The project premise being tested is that nosocomial
pathogens that colonize the intestines specifically target individuals with immature infant-like gut microbiota
features that are permissive to pathogen colonization. The notable AMR-pathogens of our study include
Clostridioides difficile, vancomycin-resistant enterococcus (VRE), carbapenem-resistant Klebsiella pneumoniae,
and extended spectrum β-lactamase producing Enterobacteriacae (ESBL-E/CRE) because these organisms
often colonize the intestines before causing infection. Specifically, we show that these priority pathogens often
co-colonize vulnerable patients who are missing keystone microbiota species that appear to be broadly
protective against these bacteria by producing diverse bacteriocins. In Project 3 of this PO1 application, we will
perform synergistic functional profiling of these unique host-microbiota-pathogen interactions to address the
following two specific aims:
• Aim 3.1. Define the metabolically active microbiota community structure identified with
pathogen colonization and disease progression in the susceptible patient.
• Aim 3.2. Characterize keystone microbiota features and their protective antimicrobial
mechanisms.
The study is impactful because we intend to establish predictive microbiome-risk algorithms for precision
infection management of immunosuppressed and critically ill patients. The long-term goal is to advise the
physician and healthcare stakeholders of clinical surveillance and therapeutic interventions that match the risk
posed by each individual’s infection, as well as define host-microbiota-pathogen interactions that are permissive
to other emerging infections.
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Project 3: Functional Microbiome and Host Signatures in Transition from Commensal to pathogen
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批准号:10226289
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项目类别:
-
资助金额:$53.95万
-
财政年份:2020
-
负责人:Tor C. Savidge
-
依托单位:
Project 3: Functional Microbiome and Host Signatures in Transition from Commensal to pathogen
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批准号:10024961
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项目类别:
-
资助金额:$49.4万
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财政年份:2020
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负责人:Tor C. Savidge
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依托单位:
Metabolome-Based Biomarkers and Neutraceuticals in Clostridium Difficile Infection
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批准号:8925055
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项目类别:
-
资助金额:$19.66万
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财政年份:2014
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负责人:Tor C. Savidge
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依托单位:
Metabolome-Based Biomarkers and Neutraceuticals in Clostridium Difficile Infection
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批准号:8822617
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项目类别:
-
资助金额:$23.6万
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财政年份:2014
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负责人:Tor C. Savidge
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依托单位:
Allosteric therapy of the Clostridium difficile toxins
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批准号:8343416
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项目类别:
-
资助金额:$10.77万
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财政年份:2012
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负责人:Tor C. Savidge
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依托单位:
Allosteric therapy of the Clostridium difficile toxins
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批准号:8609632
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项目类别:
-
资助金额:$27.48万
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财政年份:2012
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负责人:Tor C. Savidge
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依托单位:
Allosteric therapy of the Clostridium difficile toxins
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批准号:8678835
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项目类别:
-
资助金额:$39.33万
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财政年份:2012
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负责人:Tor C. Savidge
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依托单位:
Allosteric therapy of the Clostridium difficile toxins
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批准号:8890763
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项目类别:
-
资助金额:$39.33万
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财政年份:2012
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负责人:Tor C. Savidge
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依托单位:
Allosteric therapy of the Clostridium difficile toxins
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批准号:8463992
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项目类别:
-
资助金额:$36.97万
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财政年份:2012
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负责人:Tor C. Savidge
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依托单位:
S-nitrosoglutathione regulation of intestinal barrier function in Crohn's disease
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批准号:7660261
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项目类别:
-
资助金额:$18.88万
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财政年份:2009
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负责人:Tor C. Savidge
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依托单位:
海外基金