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The apoptotic potential of different HIV-1 subtype C Tat mutations in cell culture

dc.contributor.advisorEngelbrecht, Susanen_ZA
dc.contributor.advisorGlashoff, Richarden_ZA
dc.contributor.authorIsaacs, Shahiedaen_ZA
dc.contributor.otherStellenbosch University. Faculty of Medicine and Health Sciences. Dept. of Pathology. Medical Virology.en_ZA
dc.date.accessioned2013-02-26T13:17:07Zen_ZA
dc.date.accessioned2013-03-15T07:39:15Z
dc.date.available2013-02-26T13:17:07Zen_ZA
dc.date.available2013-03-15T07:39:15Z
dc.date.issued2013-03en_ZA
dc.identifier.urihttp://hdl.handle.net/10019.1/80187
dc.descriptionThesis (MScMedSc)--Stellenbosch University, 2013.en_ZA
dc.descriptionBibliography
dc.description.abstractThe efficiency in which HIV-1 can infect, spread and evade the attack of therapeutic agents can be attributed to a high mutation rate and frequent recombination events. These factors have collectively contributed to the diversity observed in HIV-1 and resulted in a multitude of subtypes, sub-subtypes, circulating recombinant forms (CRF’s) and unique recombinant forms (URF’s). The aim of this study was to investigate HIV-1 diversity in Cape Town using a small cohort of treatment naive patients being investigated for HIV Associated Neurocognitive Disorders (HAND). Four different genomic domains: gag, pol, accessory and gp41 genes were sequenced to subtype the virus. HIV-1 tat was further investigated because the dicysteine motif has been reported to play a role in HAND. Viral RNA and proviral DNA was extracted from 64 patients and used for the amplification and sequencing of the genes. Rega and jpHMM online tools were used to identify HIV-1 subtypes and recombinants while Neighbor-joining phylogenetic trees were constructed for phylogenetic analysis. The pol gene was further investigated using SCUEAL to detect possible intra-subtype recombination and was also screened for the presence of transmitted drug resistance. In addition tat sequence datasets retrieved from the Los Alamos sequence database were investigated and compared with the newly generated sequences for the detection of point mutations and amino acid signature patterns. Sequencing identified most of the samples as subtype C; however six inter-subtype recombinants (AE, A1G, A1CU and two BC) and 9 intra-subtype C recombinants were identified. In addition 13% of pol sequences were identified with resistance mutations. Signature pattern analysis identified a high level of variability in the tat sequences: 68% were identified with C30S31; 29% with the C30C31 mutation and a single sequence with a novel mutation C30A31. Functional analysis of these mutations indicated that all mutations investigated were capable of inducing apoptosis in cell culture. The C30C31 mutation generated the highest level of apoptosis, closely followed by the C30A31 mutation. However no statistical significance could be detected between tat mutations and the observed levels of apoptosis.en_ZA
dc.format.extent121 p. : ill.
dc.language.isoen_ZAen_ZA
dc.publisherStellenbosch : Stellenbosch Universityen_ZA
dc.subjectHIV diversityen_ZA
dc.subjectTat mutations in cell cultureen_ZA
dc.subjectHIV infections -- South Africa -- Preventionen_ZA
dc.subjectSubtype Cen_ZA
dc.subjectHIV infections -- South Africa -- Treatmenten_ZA
dc.subject.otherPathology -- Division of Medical Virologyen_ZA
dc.titleThe apoptotic potential of different HIV-1 subtype C Tat mutations in cell cultureen_ZA
dc.typeThesisen_ZA
dc.rights.holderStellenbosch University


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