High prevalence of pre-treatment and acquired HIV-1 drug resistance mutations among non-citizens living with HIV in Botswana.

Botswana HIV-1C acquired HIV drug resistance (ADR) antiretroviral therapy (ART) drug resistance mutations (DRMs) non-citizens pre-treament drug resistance (PDR)

Journal

Frontiers in microbiology
ISSN: 1664-302X
Titre abrégé: Front Microbiol
Pays: Switzerland
ID NLM: 101548977

Informations de publication

Date de publication:
2024
Historique:
received: 14 11 2023
accepted: 08 02 2024
medline: 13 3 2024
pubmed: 13 3 2024
entrez: 13 3 2024
Statut: epublish

Résumé

Approximately 30,000 non-citizens are living with HIV in Botswana, all of whom as of 2020 are eligible to receive free antiretroviral treatment (ART) within the country. We assessed the prevalence of HIV-1 mutational profiles [pre-treatment drug resistance (PDR) and acquired drug resistance (ADR)] among treatment-experienced (TE) and treatment-naïve (TN) non-citizens living with HIV in Botswana. A total of 152 non-citizens living with HIV were enrolled from a migrant HIV clinic at Independence Surgery, a private practice in Botswana from 2019-2021. Viral RNA isolated from plasma samples were genotyped for HIV drug resistance (HIVDR) using Sanger sequencing. Major known HIV drug resistance mutations (DRMs) in the A total of 60/152 (39.5%) participants had a detectable viral load (VL) >40 copies/mL and these were included in the subsequent analyses. The median age at enrollment was 43 years (Q1, Q3: 38-48). Among individuals with VL > 40 copies/mL, 60% (36/60) were treatment-experienced with 53% (19/36) of them on Atripla. Genotyping had a 62% (37/60) success rate - 24 were TE, and 13 were TN. A total of 29 participants (78.4, 95% CI: 0.12-0.35) had major HIV DRMs, including at least one non-nucleoside reverse transcriptase inhibitor (NNRTI) associated DRM. In TE individuals, ADR to any antiretroviral drug was 83.3% (20/24), while for PDR was 69.2% (9/13). The most frequent DRMs were nucleoside reverse transcriptase inhibitors (NRTIs) M184V (62.1%, 18/29), NNRTIs V106M (41.4%, 12/29), and K103N (34.4%, 10/29). No integrase strand transfer inhibitor-associated DRMs were reported. We report high rates of PDR and ADR in ART-experienced and ART-naïve non-citizens, respectively, in Botswana. Given the uncertainty of time of HIV acquisition and treatment adherence levels in this population, routine HIV-1C VL monitoring coupled with HIVDR genotyping is crucial for long-term ART success.

Sections du résumé

Background UNASSIGNED
Approximately 30,000 non-citizens are living with HIV in Botswana, all of whom as of 2020 are eligible to receive free antiretroviral treatment (ART) within the country. We assessed the prevalence of HIV-1 mutational profiles [pre-treatment drug resistance (PDR) and acquired drug resistance (ADR)] among treatment-experienced (TE) and treatment-naïve (TN) non-citizens living with HIV in Botswana.
Methods UNASSIGNED
A total of 152 non-citizens living with HIV were enrolled from a migrant HIV clinic at Independence Surgery, a private practice in Botswana from 2019-2021. Viral RNA isolated from plasma samples were genotyped for HIV drug resistance (HIVDR) using Sanger sequencing. Major known HIV drug resistance mutations (DRMs) in the
Results UNASSIGNED
A total of 60/152 (39.5%) participants had a detectable viral load (VL) >40 copies/mL and these were included in the subsequent analyses. The median age at enrollment was 43 years (Q1, Q3: 38-48). Among individuals with VL > 40 copies/mL, 60% (36/60) were treatment-experienced with 53% (19/36) of them on Atripla. Genotyping had a 62% (37/60) success rate - 24 were TE, and 13 were TN. A total of 29 participants (78.4, 95% CI: 0.12-0.35) had major HIV DRMs, including at least one non-nucleoside reverse transcriptase inhibitor (NNRTI) associated DRM. In TE individuals, ADR to any antiretroviral drug was 83.3% (20/24), while for PDR was 69.2% (9/13). The most frequent DRMs were nucleoside reverse transcriptase inhibitors (NRTIs) M184V (62.1%, 18/29), NNRTIs V106M (41.4%, 12/29), and K103N (34.4%, 10/29). No integrase strand transfer inhibitor-associated DRMs were reported.
Conclusion UNASSIGNED
We report high rates of PDR and ADR in ART-experienced and ART-naïve non-citizens, respectively, in Botswana. Given the uncertainty of time of HIV acquisition and treatment adherence levels in this population, routine HIV-1C VL monitoring coupled with HIVDR genotyping is crucial for long-term ART success.

Identifiants

pubmed: 38476948
doi: 10.3389/fmicb.2024.1338191
pmc: PMC10929613
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1338191

Informations de copyright

Copyright © 2024 Mokgethi, Choga, Maruapula, Moraka, Seatla, Bareng, Ditshwanelo, Mulenga, Mohammed, Kaumba, Chihungwa, Marukutira, Moyo, Koofhethile, Dickinson, Mpoloka and Gaseitsiwe.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Patrick T Mokgethi (PT)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
Department of Biological Sciences, University of Botswana, Gaborone, Botswana.

Wonderful T Choga (WT)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
Center of Epidemic Response and Innovation, Faculty of Data Sciences, Stellenbosch University, Cape Town, South Africa.
School of Allied Health Professionals, Faculty of Health Sciences, University of Botswana, Gaborone, Botswana.

Dorcas Maruapula (D)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.

Natasha O Moraka (NO)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
School of Allied Health Professionals, Faculty of Health Sciences, University of Botswana, Gaborone, Botswana.

Kaelo K Seatla (KK)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.

Ontlametse T Bareng (OT)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
School of Allied Health Professionals, Faculty of Health Sciences, University of Botswana, Gaborone, Botswana.

Doreen D Ditshwanelo (DD)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.

Graceful Mulenga (G)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.

Terence Mohammed (T)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.

Pearl M Kaumba (PM)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
Department of Biological Sciences, University of Botswana, Gaborone, Botswana.

Moses Chihungwa (M)

Independence Avenue Clinic, Gaborone, Botswana.

Tafireyi Marukutira (T)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
Public Health, Burnet Institute, Melbourne, VIC, Australia.
Department of Epidemiology, School of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia.

Sikhulile Moyo (S)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
Department of Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health, Boston, MA, United States.
School of Health Systems and Public Health, University of Pretoria, Pretoria, South Africa.
Division of Medical Virology, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa.

Catherine K Koofhethile (CK)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
Department of Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health, Boston, MA, United States.

Diana Dickinson (D)

Independence Avenue Clinic, Gaborone, Botswana.

Sununguko W Mpoloka (SW)

Department of Biological Sciences, University of Botswana, Gaborone, Botswana.

Simani Gaseitsiwe (S)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
Department of Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health, Boston, MA, United States.

Classifications MeSH