grant

CRISPR and Virulence Core

Organization UNIVERSITY OF CALIFORNIA, SAN FRANCISCOLocation SAN FRANCISCO, UNITED STATESPosted 1 Jan 2022Deadline 31 Dec 2026
NIHUS FederalResearch GrantFY2026AffectAlgorithmsAntigensApplied GeneticsAssayBioassayBioinformaticsBiological AssayC immitisC posadasiiC. immitisC. posadasiiCRISPRCRISPR approachCRISPR based approachCRISPR methodCRISPR methodologyCRISPR techniqueCRISPR technologyCRISPR toolsCRISPR-CAS-9CRISPR-based methodCRISPR-based techniqueCRISPR-based technologyCRISPR-based toolCRISPR/CAS approachCRISPR/Cas methodCRISPR/Cas systemCRISPR/Cas technologyCRISPR/Cas9CRISPR/Cas9 technologyCandidate Disease GeneCandidate GeneCas nuclease technologyCell BodyCell Culture TechniquesCellsCenters for Disease ControlCenters for Disease Control and PreventionCenters for Disease Control and Prevention (U.S.)Clustered Regularly Interspaced Short Palindromic RepeatsClustered 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 technologyCo-cultureCoccidioidesCoccidioides immitisCoccidioides posadasiiCoccidioidomycosisCocultivationCocultureCoculture TechniquesComplexDataData AnalysesData AnalysisDefectDesert rheumatismDevelopmentDiagnosticDiseaseDisease OutcomeDisorderEngineeringFungal Drug ResistanceFungus drug resistantGWA studyGWASGene DeletionGene TargetingGene TranscriptionGenesGeneticGenetic TranscriptionGoalsHumanImmuneImmunesIn VitroIncidenceInfectionLabelLaboratoriesLeadLength of StayMacrophageMarketingMethodologyMiceMice MammalsModelingModern ManMorphologyMurineMusNumber of Days in HospitalPathogenesisPathogenicityPathogenicity FactorsPathway interactionsPatientsPatternPb elementPhasePhenotypePlasmidsPlayProteinsRNA ExpressionReportingResearchResearch ProposalsRoleSan Joaquin Valley feverSisterTechnologyTestingTherapeuticTimeTranscriptTranscriptionUnited States Centers for Disease ControlUnited States Centers for Disease Control and PreventionVaccinesValley FeverVirulenceVirulence FactorsVisualization softwareWorkanti-fungal drug resistanceanti-fungal drug resistantanti-fungal resistanceanti-fungal resistantcandidate identificationcell culturecell culturescostdata interpretationdesert feverdevelop a vaccinedevelop vaccinesdevelopment of a vaccinedevelopmentalexperienceexperimentexperimental researchexperimental studyexperimentsfungal pathogenfungi pathogenfungus drug resistancegene deletion mutationgene functiongenetic approachgenetic strategygenome analysisgenome wide associationgenome wide association scangenome wide association studygenomewide association scangenomewide association studyheavy metal Pbheavy metal leadhospital dayshospital length of stayhospital stayimmunogenimprovedin vitro Assayinsightinterestmouse modelmurine modelmutantnovelpathogenpathogenic funguspathwayprogramspromoterpromotorresistance to anti-fungalresistant to anti-fungalreverse geneticssocial roletooltraitvaccine developmentvisualization toolwhole genome association analysiswhole genome association study
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Full Description

PROJECT SUMMARY/ABSTRACT
Little is known about virulence mechanisms for most emerging fungal pathogens. Coccidioides immitis and C.

posadasii, are of specific concern due to rapid increase in disease (coccidioidomycosis, aka Valley fever)

incidence in the US, with a more than 10-fold increase in reported disease over the last 20 years. The Centers

for Disease Control and Prevention (CDC) report that average cost for treating Valley fever is $50,000 per patient,

including extensive hospital stays and treatment regimes. Use of CRISPR/Cas9 and functional assessment of

targeted gene deletion on virulence can help improve our understanding of mechanisms of pathogenicity and

represent the foundational framework that is necessary for development of these approaches. We propose to

functionally delete 10 gene targets in Coccidioides posadasii strain Silveira and assay these deletions for loss of

virulence. We will further investigate pathogenicity in C. immitis strain RS for those genes that show a loss of

virulence. Currently, few specific mechanisms of virulence have been investigated in Coccidioides. Analysis of

these data will provide new insights into functions of Coccidioides genes, which will increase our understanding

of fungal pathogenesis mechanisms. Finally, we will work to develop tools to engineer fluorescently labeled live

strains for Coccidioides using mCherry expression that will increase tools for interrogating host:pathogen

interactions in an in vitro cell culture assay. In total, this proposal represents needed improvements in functional

assessment of virulence in an important, yet understudied, fungal pathogen.

Grant Number: 5U19AI166798-05
NIH Institute/Center: NIH

Principal Investigator: Bridget Barker

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