grant

P01 Administrative Core

Organization METHODIST HOSPITAL RESEARCH INSTITUTELocation HOUSTON, UNITED STATESPosted 1 Aug 2020Deadline 31 Jul 2026
NIHUS FederalResearch GrantFY2025AccelerationAccountabilityAddressAdmissionAdmission activityAdvisory CommitteesAgricultureAntibiotic AgentsAntibiotic DrugsAntibiotic ResistanceAntibioticsAntimicrobial ResistanceBenchmarkingBest Practice AnalysisBudgetsC diffC difficileC. diffC. difficileCcra beta-lactamaseClinicalClinical DataClostridioides difficileClostridium difficileColiform BacilliCollaborationsCombating Antibiotic Resistant BacteriaCommunicationCritical IllnessCritically IllDataDecision MakingDedicationsDevelopmentDisease ProgressionDisputesEffectivenessEnsureEnteric BacteriaEnterobacteriaEnterobacteriaceaeExtended-spectrum beta-lactamaseExtended-spectrum β-lactamaseGI colonizationGI commensalGI microbiotaGastrointestinal microbiotaGenomicsGoalsGovernmentHomeHuman ResourcesImmunocompromisedImmunocompromised HostImmunocompromised PatientImmunosuppressed HostIndustrializationInfectionInstitutionIntensive Care UnitsInvestigatorsLeadershipLifeLiquid substanceLogisticsMDR organismMDR pathogenManpowerMediatingMedicalMedical centerMinorMiscellaneous AntibioticModern MedicineMonitorNational Institutes of HealthOn-Line SystemsOnline SystemsOrganismPathogenicityPatientsPersonsPhenotypePositionPositioning AttributeProcessProductivityProgram ReviewsProgress ReportsProteomicsPublic HealthQuality ControlR-Series Research ProjectsR01 MechanismR01 ProgramRegimenResearchResearch ActivityResearch GrantsResearch PersonnelResearch Project GrantsResearch ProjectsResearchersResistance to antibioticsResistant to antibioticsResolutionSamplingSystemTask ForcesTechniquesTexasTherapeuticTranslatingUnited NationsUnited States National Institutes of HealthVancomycin resistant enterococcusVancomycin-resistant enterococciWorkadvisory teamanti-microbial resistantantibiotic drug resistanceantibiotic resistantbenchmarkcarbapenemaseclinical practicecommensal bacteria in the gastrointestinal tractcommensal bacteria in the gutcommensal bacteria in the intestinecommensal floracommensal microbescommensal microbiotacommensal microfloraconflict resolutiondata managementdata sharingdevelopmentaldiagnostic approachdiagnostic strategyenteric commensalenteric microbial communityenteric microbiotafluidfunctional genomicsgastrointestinalgastrointestinal commensalgastrointestinal microbial floragastrointestinal tract colonizationgut colonizationgut commensalgut communitygut floragut microbe communitygut microbial communitygut microbial compositiongut microbial consortiagut microbiotagut microbioticgut microflorahigh riskhomesimmunosuppressed patientimproved outcomeinsightintestinal colonizationintestinal commensalintestinal floraintestinal microbiotaintestinal microfloraintestinal tract microfloraliquidliving systemmeetingmeetingsmetabolism measurementmetabolomicsmetabonomicsmicrobial consortiamicrobial floramicrobiotamicrofloramicroorganismmortalitymulti-drug resistant organismmulti-drug resistant pathogenmultidrug resistant organismmultidrug resistant pathogenmultiple drug resistant organismmultiple drug resistant pathogenmultispecies consortianovelonline computeroperationoperationsoutcome predictionpathogenpersonnelprogramsresistance to anti-microbialresistant to antimicrobialresolutionssample collectionspecimen collectionsuccesssynergismtreatment strategyvancomycin resistance enterococcivancomycin resistance in enterococciweb based
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Full Description

ABSTRACT (Administrative Core)
The clinical introduction of antibiotics in 1930s-40s represented a major medical breakthrough enabling many

advances in modern medicine, agriculture and industrial practice. Unfortunately, the rise of antibiotic-resistant

microorganisms globally is now considered one of the most challenging public health threats of the 21st century.

The call for action against the threat of antibiotic resistance has now reached the highest level of government

including the Office of the US President (with the creation of the Presidential Advisory Council on Combating

Antibiotic-Resistant Bacteria) and the initiative for global action by the United Nations, among others.

Vancomycin-resistant enterococci (VRE), Enterobacteriaceae carrying extended spectrum β-lactamases and

carbapenemases (ESBL-E/CRE), and Clostridiodes difficile are particularly concerning for high-risk patients

who are immunocompromised and/or admitted to intensive care units (ICUs). Having the potential to cause life-

threatening infections, particularly in those patients who have already been subjected to multiple antibiotic

regimens, each of these organisms colonize the intestines, and their presence impacts subsequent colonization

by other pathogens further contributing to serious disease progression and even mortality in these high-risk

patients. Although these pathogens have been studied in isolation, elucidation of the dynamic interactions

between pathogens and commensal gut microbiota and their implication for predicting outcomes and,

thus, treatment strategies is more urgent than ever and requires a strategic, coordinated effort. The Texas

Medical Center in Houston, Texas is home to several world leaders in antimicrobial resistance research and

clinical practice with patient access and tremendous expertise in the cutting-edge genomic and phenotypic

techniques who are uniquely positioned to perform concerted and synergistic systems-level studies of the

multiple players that must be understood to address this challenge. These experts have recognized this

exceptional opportunity and the strength of addressing the critical and unmet challenge through the formation of

a multi-institutional collaborative research program Dynamics of Colonization and Infection by Multidrug-

Resistant Pathogens in Immunocompromised and Critically Ill Patients (DYNAMITE). Crucial for the

effectiveness of this multi-institutional research effort, is dedicated centralized administrative oversight and

support. The Administrative Core will serve as the central “hub” for program oversight, accountability,

communication, and project/process coordination for the three Projects and the Functional Genomics Core. To

achieve these goals, the Administrative Core will provide integrative accountability and oversight through the

Executive Leadership Team and the Internal and External Advisory Committees, and administrative support for

all project leaders, research personnel, key collaborators and advisors, and institutional administrative liaisons.

Grant Number: 5P01AI152999-05
NIH Institute/Center: NIH

Principal Investigator: Cesar Arias

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