High throughput measurement of envelope gene diversity for an HIV incidence assay
High throughput measurement of envelope gene diversity for an HIV incidence assay
批准号:
8717846
负责人:
Satish Kumar Pillai
金额:
$17.72万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-01-18 至 2015-12-31
关键词:
AIDS preventionBiological AssayBlood TestsCharacteristicsChronicComplementDNADNA BindingDataDisadvantagedDistantDyesEntropyEvaluationFeasibility StudiesFutureGenesGeneticGenetic VariationGoldHIVHIV InfectionsHealthcare SystemsHigh-Throughput Nucleotide SequencingHuman immunodeficiency virus testImmune responseIncidenceInfectionKineticsMeasurementMeasuresMethodsMolecular GeneticsPatientsPerformancePilot ProjectsPlasmaProceduresPublic HealthQualitative MethodsRNA-Directed DNA PolymeraseReagentRelative (related person)ResolutionSamplingT-Cell ReceptorT-Cell Receptor GenesTemperatureTestingTimeValidationViralViral Envelope GeneVirusWeightWidthbasecostdeep sequencinggenetic technologyimprovedmeltingnovel strategiespublic health relevanceresponsevirus genetics
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Estimating HIV incidence is an important challenge for public health. An assay that could reliably distinguish incident (new) HIV infections from chronic ones would be invaluable. Initial approaches to this problem have focused on the qualities of the host's humoral response to the virus. Unfortunately, assays based on this principle have been technically difficult and there are concerns about their accuracy. An alternative strategy is to measure the genetic diversity of a patient's virus, with diversity expected to be low in new HIV infections. Directly sequencing viral samples is expensive; measuring sequence diversity through high-resolution melting curves is more affordable, but it is only a qualitative method, and it may be misleading in patients with multiple founder viruses. Here, we propose to adapt a low-cost assay based on DNA hybridization kinetics, called AmpliCot, to the measurement of HIV gene complexity. The first aim of the project is to adapt and simplify the existing method (used to measure T cell receptor gene complexity) to viral envelope genes. This will require the synthesis of new measurement standards and the validation of new experimental conditions. The second aim is to determine how well AmpliCot measurements correlate with viral sequence complexity, sequence diversity, and Shannon entropy (a measure of sequence complexity weighted for relative abundance), with comparison to deep sequencing as a gold standard. The third aim is to test the predictive power of AmpliCot, high-resolution melting, or a combination of the two methods, against a test panel of plasma samples from subjects with new and chronic HIV infections. Serial samples from newly-infected HIV patients can be used to test whether the assay can detect an increase in viral genetic diversity over time. The reagents, methods and preliminary data from this pilot project will be used to support an R01 application for more extensive validation of this method.
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会议论文
Innate Sensing of Cell-Free DNA and the Interferon-Mediated Control of HIV In Vivo
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批准号:10620085
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资助金额:$29.09万
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财政年份:2023
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负责人:Satish Kumar Pillai
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Innate Sensing of Cell-Free DNA and the Interferon-Mediated Control of HIV In Vivo
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批准号:10661305
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资助金额:$27.7万
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依托单位:
Bioinformatics Core
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批准号:10614011
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资助金额:$11.91万
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财政年份:2022
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负责人:Satish Kumar Pillai
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Bioinformatics Core
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批准号:10459931
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资助金额:$12.74万
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财政年份:2022
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Project 3: Identifying plasma biomarkers predicting time to HIV rebound after treatment interruption
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批准号:10223997
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资助金额:$39.58万
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财政年份:2017
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负责人:Satish Kumar Pillai
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依托单位:
Effects of Cell-Intrinsic Immunity on Establishment and Reversal of HIV Latency
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批准号:9354580
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项目类别:
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资助金额:$12.5万
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财政年份:2015
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负责人:Satish Kumar Pillai
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依托单位:
Effects of Cell-Intrinsic Immunity on Establishment and Reversal of HIV Latency
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批准号:9134183
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资助金额:$30.48万
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财政年份:2015
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负责人:Satish Kumar Pillai
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依托单位:
High throughput measurement of envelope gene diversity for an HIV incidence assay
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批准号:8720184
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项目类别:
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资助金额:$22.71万
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财政年份:2013
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负责人:Satish Kumar Pillai
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依托单位:
High throughput measurement of envelope gene diversity for an HIV incidence assay
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批准号:8466485
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项目类别:
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资助金额:$0.0万
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财政年份:2013
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负责人:Satish Kumar Pillai
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依托单位:
Characterization of the HIV-1 Latent Reservoir in CCR5-Delta 32 Heterozygotes
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批准号:8603539
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项目类别:
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资助金额:$22.24万
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财政年份:2013
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负责人:Satish Kumar Pillai
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依托单位:
Antiviral Role of APOBEC3 in HIV/HCV Coinfected Patients
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批准号:8760584
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项目类别:
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资助金额:$6.21万
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财政年份:2008
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负责人:Satish Kumar Pillai
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依托单位:
Antiviral Role of APOBEC3 in HIV/HCV Coinfected Patients
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批准号:7615163
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项目类别:
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资助金额:$18.04万
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财政年份:2008
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负责人:Satish Kumar Pillai
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依托单位:
Antiviral Role of APOBEC3 in HIV/HCV Coinfected Patients
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批准号:8067032
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项目类别:
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资助金额:$18.04万
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财政年份:2008
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负责人:Satish Kumar Pillai
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依托单位:
Antiviral Role of APOBEC3 in HIV/HCV Coinfected Patients
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批准号:8242881
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项目类别:
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资助金额:$11.8万
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财政年份:2008
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负责人:Satish Kumar Pillai
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依托单位:
Antiviral Role of APOBEC3 in HIV/HCV Coinfected Patients
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批准号:7419454
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项目类别:
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资助金额:$18.04万
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财政年份:2008
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负责人:Satish Kumar Pillai
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依托单位:
Antiviral Role of APOBEC3 in HIV/HCV Coinfected Patients
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批准号:7817125
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项目类别:
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资助金额:$18.04万
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财政年份:2008
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负责人:Satish Kumar Pillai
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依托单位:
Project 3: Identifying plasma biomarkers predicting time to HIV rebound after treatment interruption
-
批准号:9754770
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项目类别:
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资助金额:$39.58万
-
财政年份:--
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负责人:Satish Kumar Pillai
-
依托单位:
Project 3: Identifying plasma biomarkers predicting time to HIV rebound after treatment interruption
-
批准号:9539963
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项目类别:
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资助金额:$39.58万
-
财政年份:--
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负责人:Satish Kumar Pillai
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依托单位:
海外基金