Awardee OrganizationRUTGERS BIOMEDICAL AND HEALTH SCIENCES
Description
Abstract Text
ABSTRACT
Fungal species are among the most common causes of nosocomial bloodstream and invasive infections in
immunocompromised hosts. Mortality from candidemia can be very high, ranging from 20-40%. Cryptococcus
affects approximately 2-3% of solid organ transplant patients and Cryptococcus gattii has emerged as a new
cause of pneumonia and disseminated fungal disease. The global emergence of virulent multidrug resistant
species such as Candida auris, with a mortality reported to be as high as 68% is particularly worrisome. Culture-
based tests to detect Candida infections are slow, relatively insensitive, and may have difficulty distinguishing
between C. auris and other related Candida species. Lateral flow antigen tests for Cryptococcus have high
sensitivity and specificity but Cryptococcal antigen detection is available only as a standalone assay that is not
part of a larger fungal panel; thus, Cryptococcus infections may be missed in the absence of clinical suspicion.
Nucleic acid amplification based Candida assays do not have the sensitivity required to detect a Candida
infection directly from a patient blood sample (without pre-culture amplification) except for the T2Candida test
(based on magnetic resonance technology), which is prohibitively expensive, slow, low throughput and is only
able to distinguish among a limited number of Candida species. A more widely available, more rapid and user
friendly, and less expensive test for fungal blood stream infections has the potential to greatly impact patient
care and improve infection control. This proposal will take advantage of years of successful collaborations
between the Alland laboratory and Cepheid developing point of care diagnostic assays, including new
approaches to large blood volume sample processing and ultra-sensitive DNA sequence detection. We will
leverage this experience to create a fungal detection assay with unparalleled performance. Our specific aims
are: 1) Assay development. 2) Improved sample processing to maximize test blood volume and enhance assay
sensitivity. 3) Development and testing using dried reagent beads. 4) Perform analytic and pre-clinical studies in
preparation for large-scale clinical trials.
Public Health Relevance Statement
PROJECT NARRATIVE
This project will develop a highly specific, sensitive, rapid, and easy to use a point of care test to rapidly
detect blood stream infections due to the fungi Candida and Cryptococcus including Candida auris and
Cryptococcus gattii, newly emerging diseases. This research will benefit public health by increasing the speed
that these infections can be detected, ensuring that the best treatment for each specific infecting organism is
selected.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AffectBacteriaBiological AssayBloodBlood CirculationBlood TestsBlood VolumeBlood specimenBuffersCandidaCandida albicansCandida aurisCandida glabrataCerebrospinal FluidCessation of lifeClinicalClinical TrialsCodeCollaborationsCommunicable DiseasesCryptococcusCryptococcus gattiiCryptococcus neoformansDNA SequenceDetectionDevelopmentDiagnosisDiagnosticDiseaseDrynessEnsureFDA approvedFreeze DryingFungemiaHIVImmunocompromised HostIndividualInfectionInfection ControlLaboratoriesLateralLifeMagnetic ResonanceMedical Care CostsMethodsMoldsMulti-Drug ResistanceMycosesNested PCRNucleic AcidsOrganismPacific NorthwestPatient CarePatientsPerformancePhasePneumoniaPreparationProbabilityProcessPublic HealthReactionReagentReportingResearchRiskSamplingSensitivity and SpecificitySerumSignal TransductionSolidSpecificitySpeedStaphylococcus aureusStreamTechnologyTemperatureTestingTimeTrainingUnited StatesVirulentamplification detectionantigen detectionantigen testassay developmentbasecandidemiaclinically relevantdesigndetection assaydiagnostic assayeffective therapyexperiencefungusimprovedinnovationlow and middle-income countriesmeltingmortalitynovel strategiesorgan transplant recipientpandemic diseasepoint of carepoint of care testingpoint-of-care diagnosticspreclinical studyprototyperapid detectionrapid diagnosistesting accesstreatment durationuser-friendly
National Institute of Allergy and Infectious Diseases
CFDA Code
855
DUNS Number
090299830
UEI
YVVTQD8CJC79
Project Start Date
16-January-2020
Project End Date
31-December-2025
Budget Start Date
01-January-2024
Budget End Date
31-December-2025
Project Funding Information for 2024
Total Funding
$764,715
Direct Costs
$555,044
Indirect Costs
$209,671
Year
Funding IC
FY Total Cost by IC
2024
National Institute of Allergy and Infectious Diseases
$764,715
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5R01AI148437-05
Publications
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Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
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Clinical Studies
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History
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