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Proteomic insights into the modulation of foetal neurogenesis by the anti-retroviral efavirenz

Background: South African guidelines recommend that HIV-positive pregnant women immediately initiate antiretroviral therapy (efavirenz, emtricitabine, and tenofovir), regardless of trimester. Efavirenz causes central nervous system neuropathy and has been linked to birth defects such as encephalocoe...

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Main Author: Albeldas, Claudia
Other Authors: Blackburn, Jonathan
Format: Thesis
Language:English
Published: Department of Integrative Biomedical Sciences 2020
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access_status_str Open Access
author Albeldas, Claudia
author2 Blackburn, Jonathan
author_browse Albeldas, Claudia
Blackburn, Jonathan
author_facet Blackburn, Jonathan
Albeldas, Claudia
author_sort Albeldas, Claudia
collection Thesis
description Background: South African guidelines recommend that HIV-positive pregnant women immediately initiate antiretroviral therapy (efavirenz, emtricitabine, and tenofovir), regardless of trimester. Efavirenz causes central nervous system neuropathy and has been linked to birth defects such as encephalocoele. Cohort studies of HIV-uninfected children exposed to antiretroviral treatment in utero report minor learning delays but are inconclusive. Non-transformed human derived neuroepithelial stem (NES) represent a unique pre-clinical model in which to investigate the effects of efavirenz on the developing neural system. Efavirenz-induced global cellular molecular changes may be characterised using mass spectrometry (MS). Aims: To optimise an MS-based efavirenz extraction and detection assay, and to investigate efavirenzinduced NES proteomic responses. Methods: A TSQ Vantage triple quadrupole mass spectrometer was employed to optimise targeted detection of efavirenz extracted from cultured cells and supernatant. Cells were cultured for 72 hours, incorporating a 24-hourly efavirenz treatment. Efavirenz concentration dynamics were assessed over this period, and cells were harvested every 24 hours for discovery proteomic analysis using a Q-Exactive quadrupole-Orbitrap mass spectrometer. Results: Drug extraction with acetonitrile was selected as the optimal extraction and detection technique. In cell culture, efavirenz concentration increased after 24 hours and decreased after 48 hours. A total of 1663 protein groups were identified, with 26, 39, and 80 protein groups differentially expressed 24, 48, and 72 hours respectively post EFV treatment. The most significantly enriched deregulated pathways included cholesterol biosynthesis, mRNA splicing, and JAK/STAT and Wnt signalling. Conclusions: Efavirenz-altered protein expression reflects functional pathway perturbations, which may contribute to clinically-observed neurological effects. Orthoganal and in vivo confirmation is required.
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license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2020
publishDateRange 2020
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spelling oai:open.uct.ac.za:11427/31111 Proteomic insights into the modulation of foetal neurogenesis by the anti-retroviral efavirenz Albeldas, Claudia Blackburn, Jonathan Medicine Background: South African guidelines recommend that HIV-positive pregnant women immediately initiate antiretroviral therapy (efavirenz, emtricitabine, and tenofovir), regardless of trimester. Efavirenz causes central nervous system neuropathy and has been linked to birth defects such as encephalocoele. Cohort studies of HIV-uninfected children exposed to antiretroviral treatment in utero report minor learning delays but are inconclusive. Non-transformed human derived neuroepithelial stem (NES) represent a unique pre-clinical model in which to investigate the effects of efavirenz on the developing neural system. Efavirenz-induced global cellular molecular changes may be characterised using mass spectrometry (MS). Aims: To optimise an MS-based efavirenz extraction and detection assay, and to investigate efavirenzinduced NES proteomic responses. Methods: A TSQ Vantage triple quadrupole mass spectrometer was employed to optimise targeted detection of efavirenz extracted from cultured cells and supernatant. Cells were cultured for 72 hours, incorporating a 24-hourly efavirenz treatment. Efavirenz concentration dynamics were assessed over this period, and cells were harvested every 24 hours for discovery proteomic analysis using a Q-Exactive quadrupole-Orbitrap mass spectrometer. Results: Drug extraction with acetonitrile was selected as the optimal extraction and detection technique. In cell culture, efavirenz concentration increased after 24 hours and decreased after 48 hours. A total of 1663 protein groups were identified, with 26, 39, and 80 protein groups differentially expressed 24, 48, and 72 hours respectively post EFV treatment. The most significantly enriched deregulated pathways included cholesterol biosynthesis, mRNA splicing, and JAK/STAT and Wnt signalling. Conclusions: Efavirenz-altered protein expression reflects functional pathway perturbations, which may contribute to clinically-observed neurological effects. Orthoganal and in vivo confirmation is required. 2020-02-14T07:46:45Z 2020-02-14T07:46:45Z 2019 2020-02-14T07:46:31Z Master Thesis Masters MSc http://hdl.handle.net/11427/31111 eng application/pdf Department of Integrative Biomedical Sciences Faculty of Health Sciences
spellingShingle Medicine
Albeldas, Claudia
Proteomic insights into the modulation of foetal neurogenesis by the anti-retroviral efavirenz
thesis_degree_str Master's
title Proteomic insights into the modulation of foetal neurogenesis by the anti-retroviral efavirenz
title_full Proteomic insights into the modulation of foetal neurogenesis by the anti-retroviral efavirenz
title_fullStr Proteomic insights into the modulation of foetal neurogenesis by the anti-retroviral efavirenz
title_full_unstemmed Proteomic insights into the modulation of foetal neurogenesis by the anti-retroviral efavirenz
title_short Proteomic insights into the modulation of foetal neurogenesis by the anti-retroviral efavirenz
title_sort proteomic insights into the modulation of foetal neurogenesis by the anti retroviral efavirenz
topic Medicine
url http://hdl.handle.net/11427/31111
work_keys_str_mv AT albeldasclaudia proteomicinsightsintothemodulationoffoetalneurogenesisbytheantiretroviralefavirenz