DEVELOPMENT OF A CELL CULTURE, SCREENING, AND SEQUENCING METHOD FOR HIGH-THROUGHPUT ISOLATION OF HIV-POSITIVE CD4+ T-CELLS FROM HIV-INFECTED PATIENTS

dc.contributor.advisorSylvain Laverdure, PhD
dc.contributor.authorWhitney Bruchey
dc.contributor.departmentHood College Biology
dc.contributor.programHood College Biomedical and Environmental Science
dc.date.accessioned2024-04-26T20:04:49Z
dc.date.available2024-04-26T20:04:49Z
dc.date.issued2024
dc.description.abstractHuman immunodeficiency virus type 1 (HIV-1) is a retrovirus that targets immune cells critical to innate and adaptive immune responses in infected patients. Despite viremia suppression by antiretroviral drug treatments, chronic immune activation persists in HIV-1-infected patients, increasing their risk of HIV-associated chronic comorbidities. Defective HIV-1 proviruses harboring genetic mutations may contribute to persistent immune activation in suppressed HIV-1-infected patients through expression of canonical or novel viral proteins. In this study, we presented the steps taken to develop optimal culture conditions for CD4+ T cells from suppressed HIV-infected patients, and an unbiased nested polymerase chain reaction (PCR) approach for screening of HIV-1 positive cells. Of the 507 potential HIV-1 positive clones detected, we chose three for further bioinformatic analysis that resulted in observation of two novel open reading frames within HIV-1 integrase and reverse transcriptase genes.
dc.format.extent57 pages
dc.genreMaster’s thesis
dc.identifierdoi:10.13016/m2ale8-blkg
dc.identifier.urihttp://hdl.handle.net/11603/33319
dc.language.isoen_US
dc.rightsAttribution 3.0 United Statesen
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/
dc.subjectHIV/AIDS
dc.titleDEVELOPMENT OF A CELL CULTURE, SCREENING, AND SEQUENCING METHOD FOR HIGH-THROUGHPUT ISOLATION OF HIV-POSITIVE CD4+ T-CELLS FROM HIV-INFECTED PATIENTS
dc.typeText

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