grant

Novel Antimalarials from Fungi

Organization UNIVERSITY OF CENTRAL FLORIDALocation ORLANDO, UNITED STATESPosted 18 May 2020Deadline 30 Apr 2027
NIHUS FederalResearch GrantFY20240-11 years oldAddressAnti-Infective AgentsAnti-Infective DrugsAnti-InfectivesAnti-infective PreparationAnti-malarialsAppearanceAreaArtemisininsBio-InformaticsBioinformaticsBiologicalBurmaCRISPR approachCRISPR based approachCRISPR methodCRISPR methodologyCRISPR techniqueCRISPR technologyCRISPR toolsCRISPR-CAS-9CRISPR-based methodCRISPR-based techniqueCRISPR-based technologyCRISPR-based toolCRISPR/CAS approachCRISPR/Cas methodCRISPR/Cas technologyCRISPR/Cas9CRISPR/Cas9 technologyCaliforniaCas nuclease technologyCellular biologyCessation of lifeChemicalsChildChild YouthChildhoodChildren (0-21)ClassificationClinicalClustered Regularly Interspaced Short Palindromic Repeats approachClustered Regularly Interspaced Short Palindromic Repeats methodClustered Regularly Interspaced Short Palindromic Repeats methodologyClustered Regularly Interspaced Short Palindromic Repeats techniqueClustered Regularly Interspaced Short Palindromic Repeats technologyCombined Modality TherapyCopy Number PolymorphismCountryDataDeathDevelopmentDiseaseDisorderDrug KineticsDrug resistanceDrugsESI Mass SpectrometryEconomicsEffectivenessEvolutionFilamentous FungiFloridaGeneralized GrowthGenetic AlterationGenetic ChangeGenetic defectGrowthHPLCHigh Performance Liquid ChromatographyHigh Pressure Liquid ChromatographyHigh Speed Liquid ChromatographyIn VitroIn vivo analysisIndividualInterdisciplinary ResearchInterdisciplinary StudyLaboratoriesLeadLibrariesLiverMalariaMeasuresMediatingMedicationMedicineMethodsMiceMice MammalsModelingMoldsMolecular TargetMulti-Drug ResistanceMultidisciplinary CollaborationMultidisciplinary ResearchMultidrug ResistanceMultimodal TherapyMultimodal TreatmentMultiple Drug ResistanceMultiple Drug ResistantMurineMusMutationMyanmarNMR SpectrometerNMR SpectroscopyNatural ProductsNatural Products ChemistryNatural SelectionsNatureOklahomaPaludismParasite resistanceParasitesPb elementPersonsPharmaceutical PreparationsPharmacokineticsPharmacologyPhenotypePlasmodium InfectionsPopulationPredispositionPrevalencePropertyProteinsProteomeResearchResearch ResourcesResearch SpecimenResistanceResistance profileResistance to Multi-drugResistance to MultidrugResistance to Multiple DrugResistant profileResistant to Multiple DrugResistant to multi-drugResistant to multidrugResolutionResource DevelopmentResourcesSourceSoutheast AsiaSoutheastern AsiaSpecimenSpectrometry, Mass, Electrospray IonizationStructureSusceptibilitySystematicsTexasTherapeuticTimeTissue GrowthUniversitiesValidationViet NamVietnamanti-malarial agentsanti-malarial drugsarteannuinartemisininebiologiccell biologycellular targetingcombination therapycombined modality treatmentcombined treatmentcommunicable disease control agentcomparativecopy number variantcopy number variationdetermine efficacydevelopmentaldisease controldisorder controldrug discoverydrug resistantdrug/agenteconomicefficacy analysisefficacy assessmentefficacy determinationefficacy evaluationefficacy examinationefficacy studyentire genomeevaluate efficacyexamine efficacyexperiencefull genomefungusgenome editinggenome mutationgenome sequencinggenomic editingglobal healthheavy metal Pbheavy metal leadhepatic body systemhepatic organ systemimprovedin vivoin vivo evaluationin vivo testingkidsmacromoleculemortalitymulti-drug resistantmulti-modal therapymulti-modal treatmentmultidrug resistantnaturally occurring productnew drug treatmentsnew drugsnew pharmacological therapeuticnew therapeuticsnew therapynext generationnext generation therapeuticsnovelnovel drug treatmentsnovel drugsnovel lead compoundnovel pharmaco-therapeuticnovel pharmacological therapeuticnovel therapeuticsnovel therapynuclear magnetic resonance spectroscopyontogenyparasite resistantpediatricpharmacologicpharmacophoreqinghaosuquing hau sauquinghaosuresistance strainresistance to Drugresistance to Parasiteresistantresistant parasiteresistant strainresistant to Drugresistant to Parasiteresolutionsscaffoldscaffoldingscreeningscreeningssecondary metabolitesmall molecule therapeuticstargeted drug therapytargeted drug treatmentstargeted therapeutictargeted therapeutic agentstargeted therapytargeted treatmentvalidationswhole genomeyoungster
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Full Description

Malaria still afflicts about half of the world population causing more than 400,000 deaths, mostly
children. The global economic toll of malaria is enormous. Most of the drugs that are currently

utilized for malaria treatment, including artemisinin-based combination treatments are losing

their effectiveness due to widespread emergence of drug resistance. To address the fragility of

malaria therapy, we propose to discover novel antimalarial compounds through screening of a

library of fungal secondary metabolites. We hypothesize that fungal secondary metabolites, which

are underexplored for antimalarial discovery, will provide us with a unique opportunity to

investigate medicinally relevant but untapped chemical space for the discovery of novel malaria

therapeutics. Premise for this proposal is based on our promising preliminary screen that has

identified fungal extracts and pure compounds of fungal origin with potent antiplasmodial activities.

To prove this hypothesis, we propose herein to (1) Screen a library of 10,000 extracts derived

from diverse fungal species and dereplicate prioritized bioactive extracts to identify and

determine structures of selective antiplasmodial compounds that are active against multiple

parasite developmental stages; hits will be screened to determine cross-resistance, and killing

rate. (2) Active compounds will be prioritized by in vitro physicochemical, in vivo pharmacology

and in vivo efficacy studies. (3) Target identification of prioritized hits will be determined by in

vitro evolution of resistance followed by whole genome sequencing. Target validation will be

conducted by CRISPR/Cas9 mediated genome editing. The research in this endeavor will be

conducted through a multidisciplinary collaboration between the laboratories of Debopam

Chakrabarti (University of Central Florida), Robert Cichewicz (University of Oklahoma), Kirsten

Hanson (University of Texas San Antonio), Elizabeth Winzeler and Jeremiah Momper

(University of California San Diego) with combined expertise in natural product chemistry,

malaria cell biology, anti-infective discovery, target identification, and validation. This is a highly

significant endeavor, as we will discover novel lead compounds with validated targets for

therapy against multidrug resistant malaria.

Grant Number: 5R01AI154777-05
NIH Institute/Center: NIH

Principal Investigator: DEBOPAM CHAKRABARTI

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