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Evaluation of the potential impact of multi-class Antiretroviral drug resistant variants on newly approved Antiretroviral Therapy (ART) among people living with HIV in Botswana

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dc.contributor.supervisor Nkwe, David O
dc.contributor.author Ndlovu, Nokuthula S
dc.date.accessioned 2025-08-21T08:50:20Z
dc.date.available 2025-08-21T08:50:20Z
dc.date.issued 2023-11
dc.identifier.citation Ndlovu, N.S.(2023) Evaluation of the potential impact of multi-class Antiretroviral drug resistant variants on newly approved Antiretroviral Therapy (ART) among people living with HIV in Botswana, Masters Theses, Botswana International University of Science and Technology: Palapye en_US
dc.identifier.uri https://repository.biust.ac.bw/handle/123456789/633
dc.description Thesis (MSc Biological Sciences and Biotechnology)--Botswana International University of Science and Technology, 2023 en_US
dc.description.abstract Botswana has over the years reported a rise in cases of HIV-associated drug resistance to all four available drug classes. This multi-class drug resistance is associated with virologic failure and increased disease progression, which significantly reduces antiretroviral drug (ARV) choices,especially in settings with limited treatment options. This highlights the need to monitor the emergence and spread of drug resistance, to avoid selection of ineffective ART regimens. This study therefore sought to determine the prevalence of multi-class drug resistance and determine if second generation non-nucleoside reverse transcriptase inhibitors (NNRTIs) [Doravirine (DOR), Etravarine (ETR) and Rilpivirine (RPV)] and entry inhibitors [Maraviroc (MVC), Enfuvirtide (T20) and Fostemsavir (FTR)] can be used as alternative therapy for individuals with multi-class drug resistance. Four approaches were used to analyze a total of 7473 HIV sequences: (i) the Stanford HIV drug resistance database to evaluate multi-class drug resistance and resistance to DOR, ETR and RPV; (ii) computational evaluation of MVC resistance by determining CXCR4 coreceptor usage using geno2pheno, webPSSM and the 11/25 rule; (iii) using the 2023 IAS mutations update to determine T20 resistance; and (iv) determining FTR resistance by probing previous studies that published FTR-resistance associated mutations. The proportions of drug resistance mutations (DRMs) were estimated using binomial exact methods. Predictors of multi drug resistance were determined using the univariate and multivariate logistic regression hazard models. The prevalence of multi-class drug resistance (MDR) was 682/7473 (9.1%: 95 % CI; 8.3-9.6). High prevalence of resistance to second generation NNRTIs was observed within the MDR group at the following rates: 79.3%, 63.6 % and 67.1% for RPV, ETR, and DOR, respectively.For entry inhibitors, 7.9% (31/391) CXCR4 coreceptor usage was observed, indicating low prevalence of MVC resistance. A total of 113/626 (18.1%) MDR variants presented FTR resistance. T20 resistance was observed in 313/623 (50.2%) of MDR variants. ART experience, virologic failure at viral load of >400 copies/mL and being male were significantly associated with developing MDR. This study reports high resistance to second generation NNRTIs and T20 which reduces their potential use as alternative therapy for people living with HIV who harbor MDR variants in Botswana. In contrast, low prevalence of FTR and MVC resistance allows for their potential use as alternative therapy for MDR individuals, although genotypic testing prior to use of these drugs would be necessary in order to avoid selection of ineffective ARV regimens. en_US
dc.description.sponsorship Botswana International University of Science and Technology (BIUST) en_US
dc.language.iso en en_US
dc.publisher Botswana International University of Science and Technology (BIUST) en_US
dc.subject Second generation NNRTIs en_US
dc.subject Maraviroc (MVC) en_US
dc.subject Fostemsavir (FTR) en_US
dc.subject Virologic failure en_US
dc.title Evaluation of the potential impact of multi-class Antiretroviral drug resistant variants on newly approved Antiretroviral Therapy (ART) among people living with HIV in Botswana en_US
dc.description.level msc en_US
dc.description.accessibility unrestricted en_US
dc.description.department bsb en_US


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