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The transmitted HIV-1 subtype C: characterization of the transmitted/founder full-length virus genome and the influence of early immune selective pressure on virus replication

Includes bibliographical references.

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Bibliographic Details
Main Author: Abrahams, Melissa-Rose Hilda
Other Authors: Williamson, Carolyn
Format: Thesis
Language:English
Published: Department of Clinical Laboratory Sciences 2015
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access_status_str Open Access
author Abrahams, Melissa-Rose Hilda
author2 Williamson, Carolyn
author_browse Abrahams, Melissa-Rose Hilda
Williamson, Carolyn
author_facet Williamson, Carolyn
Abrahams, Melissa-Rose Hilda
author_sort Abrahams, Melissa-Rose Hilda
collection Thesis
description Includes bibliographical references.
format Thesis
id oai:open.uct.ac.za:11427/12712
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:32:27.580Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2015
publishDateRange 2015
publishDateSort 2015
publisher Department of Clinical Laboratory Sciences
publisherStr Department of Clinical Laboratory Sciences
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/12712 The transmitted HIV-1 subtype C: characterization of the transmitted/founder full-length virus genome and the influence of early immune selective pressure on virus replication Abrahams, Melissa-Rose Hilda Williamson, Carolyn Includes bibliographical references. The identification of targets of early immune responses associated with control of HIV-1 infection will inform immunogen design for vaccine interventions. The early evolution of transmitted/founder subtype C virus sequences was investigated to determine the location and frequency of immune selection, and the impact of early immune escape mutations on viral replicative capacity. Single-genome amplified env sequences from 26 acutely-infected women were evaluated for conformance to a model of random evolution to elucidate multiplicity of infection. Near fulllength genome sequences from the first six months of infection were generated for five women and sites evolving under immune selection were mapped. CD8+ cytotoxic Tlymphocyte escape mutations in HLA-B-restricted epitopes were introduced into infectious molecular clones of cognate transmitted/founder viruses by site-directed mutagenesis and their impact on viral replicative fitness was evaluated using parallel replication assays. In 77% of women (n=20) a single transmitted/founder variant established infection and two to five variants in the remaining 23% (n=6). Near full-length genome sequencing in five women confirmed single variant/low-diversity transmission and identified fifty-five genome regions evolving under immune selection, 40% of which was attributed to CD8+ cytotoxic Tlymphocyte pressure, 35% to antibody-mediated pressure, 16% to reversion and 9% could not be classified. The rate of sequence diversification and number of sites evolving under immune selection was highest in nef. The majority of evolving CD8+ cytotoxic T-lymphocyte epitopes (82%) contained shuffling/toggling mutations. A novel B*15:10-associated mutation, A164T, combined with a V85A Pol mutation reduced viral replication capacity in one individual. In a second individual, the attenuating HLA-B*58:01-associated mutation, T242N, enhanced viral replication capacity due to pre-existing compensatory polymorphisms in the transmitted/founder virus. A third individual, who had extremely rapid disease progression, was infected with the virus with the highest replication capacity. This thesis describes the complex nature of early immune selection and escape in transmitted/founder viruses. Although attenuating escape mutations were identified in viruses from two individuals, this was not associated with clinical benefit. The extensive variability of epitopes evolving under early selection may implicate many early immune targets as poor candidates for vaccine immunogens; however some early targets may be useful if clinical benefit is conferred through attenuating escape mutations. 2015-05-04T07:06:44Z 2015-05-04T07:06:44Z 2014 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/12712 eng application/pdf Department of Clinical Laboratory Sciences Faculty of Health Sciences University of Cape Town
spellingShingle Abrahams, Melissa-Rose Hilda
The transmitted HIV-1 subtype C: characterization of the transmitted/founder full-length virus genome and the influence of early immune selective pressure on virus replication
thesis_degree_str Doctoral
title The transmitted HIV-1 subtype C: characterization of the transmitted/founder full-length virus genome and the influence of early immune selective pressure on virus replication
title_full The transmitted HIV-1 subtype C: characterization of the transmitted/founder full-length virus genome and the influence of early immune selective pressure on virus replication
title_fullStr The transmitted HIV-1 subtype C: characterization of the transmitted/founder full-length virus genome and the influence of early immune selective pressure on virus replication
title_full_unstemmed The transmitted HIV-1 subtype C: characterization of the transmitted/founder full-length virus genome and the influence of early immune selective pressure on virus replication
title_short The transmitted HIV-1 subtype C: characterization of the transmitted/founder full-length virus genome and the influence of early immune selective pressure on virus replication
title_sort transmitted hiv 1 subtype c characterization of the transmitted founder full length virus genome and the influence of early immune selective pressure on virus replication
url http://hdl.handle.net/11427/12712
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