Low prevalence of archived integrase strand transfer inhibitors resistance associated mutations in Botswana before the roll out of dolutegravir based first line antiretroviral therapy
dc.contributor.author | Maruapula, Dorcas | |
dc.contributor.author | Ditshwanelo, Doreen | |
dc.contributor.author | Pema, Marea N. | |
dc.contributor.author | Bareng, Ontlametse T. | |
dc.contributor.author | Choga, Wonderful T. | |
dc.contributor.author | Moraka, Natasha O. | |
dc.contributor.author | Mokgethi, Patrick T. | |
dc.contributor.author | Seatla, Kaelo K. | |
dc.contributor.author | Koofhethile, Catherine K. | |
dc.contributor.author | Zuze, Boitumelo | |
dc.contributor.author | Gaolathe, Tendani | |
dc.contributor.author | Pretorius-Holme, Molly | |
dc.contributor.author | Lebani, Kebaneilwe | |
dc.contributor.author | Makhema, Joseph | |
dc.contributor.author | Novitsky, Vlad | |
dc.contributor.author | Shapiro, Roger | |
dc.contributor.author | Lockman, Shahin | |
dc.contributor.author | Moyo, Sikhulile | |
dc.contributor.author | Gaseitsiwe, Simani | |
dc.date.accessioned | 2024-12-04T05:36:23Z | |
dc.date.available | 2024-12-04T05:36:23Z | |
dc.date.issued | 2024-10 | |
dc.description | DATA AVAILABITY STATEMENT: Publicly available datasets were analyzed in this study. This data can be found here: HIV-1 sequences are available on request through the PANGEA consortium (www.pangea-hiv.org). BCPP data are available at https://data.cdc.gov/Global-Health/BotswanaCombination-Prevention-Project-BCPP-Publi/qcw5-4m9q. | en_US |
dc.description.abstract | BACKGROUND: We evaluated the prevalence of archived proviral drug resistance mutations (DRMs) associated with resistance to integrase strand transfer inhibitors (INSTIs) shortly before Botswana transitioned in 2016 to using dolutegravir (DTG)-based antiretroviral treatment in first-line regimens. METHODS: We used the Stanford University HIV drug resistance database to analyze INSTI-resistance associated mutations (RAMs) in a large representative population-based cohort of adults recruited in 30 geographically dispersed communities as part of the Botswana Combination Prevention Project (BCPP) cohort from 2013 to 2018. A total of 5,144 HIV-1 proviral DNA sequences were included in our analysis; 1,281 sequences were from antiretroviral therapy (ART)-naïve individuals and 3,863 sequences were from non-nucleoside reverse transcriptase inhibitor (NNRTI) ART-experienced individuals. None of the sequences were from DTG-ART experienced participants. RESULTS: The overall prevalence of major INSTIs DRMs was 1.11% (95% CI 0.82–1.39%). The prevalence of INSTI DRMs in ART-naïve individuals was 1.64% (21/1,281) and 0.93% (36/3,863) in ART-experienced individuals. Major INSTI-RAMs detected in ART-naïve individuals were E138K (2/1,281; 0.16%), G140R (8/1,281;0.62%), E92G (2/1,281;0.16%), R263K (5/1,281; 0.4%), N155H (1/1,281; 0.08%), P145S (1/1,281;0.008%). Among the ART-experienced individuals, major INSTI RAMs detected were E138K (4/3,863; 0.10%), G140R (25/3,863;0.65%), G118R (2/3,863, 0.05%), R263K (4/3,863, 0.10%), T66I (1/3,863;0.03%), E138K + G140R (1/3,863, 0.03%|), G140R + R263K (1/3,863, 0.03%). High-level resistance to cabotegravir (CAB), elvitegravir (EVG), and raltegravir (RAL) was detected in 0.70, 0.16 and 0.06% of the individuals, respectively. Notably, bictegravir (BIC) and dolutegravir (DTG) showed no high-level resistance. CONCLUSION: The overall prevalence of archived INSTI RAMs in Botswana was low prior to transitioning to first-line DTG-based ART regimens, and did not differ between ART-naïve and ART-experienced individuals. Ongoing surveillance of INSTI DRMs in Botswana will allow for re-assessment of INSTI resistance risk following nationwide DTG rollout. | en_US |
dc.description.department | School of Health Systems and Public Health (SHSPH) | en_US |
dc.description.sdg | SDG-03:Good heatlh and well-being | en_US |
dc.description.sponsorship | The President’s Emergency Plan for AIDS Relief, the Sub-Saharan African Network for TB/HIV Research Excellence from the Bill & Melinda Gates Foundation, the Fogarty International Center at the US National Institutes of Health Award, the Fogarty International Center at the US National Institutes of Health Award, the European Union, the Trials of Excellence in Southern Africa, Africa Research Excellence Fund Research Development Fellowship. | en_US |
dc.description.uri | https://www.frontiersin.org/journals/microbiology | en_US |
dc.identifier.citation | Maruapula, D., Ditshwanelo, D., Pema, M.N., Bareng, O.T., Choga, W.T., Moraka, N.O., Mokgethi, P.T., Seatla, K.K., Koofhethile, C.K., Zuze, B.J., Gaolathe, T., Pretorius-Holme, M., Lebani, K., Makhema, J., Novitsky, V., Shapiro, R., Lockman, S.., Moyo, S. & Gaseitsiwe, S. (2024) Low prevalence of archived integrase strand transfer inhibitors resistance associated mutations in Botswana before the roll out of dolutegravir based first line antiretroviral therapy. Frontiers in Microbiology 15:1482348. doi: 10.3389/fmicb.2024.1482348 | en_US |
dc.identifier.issn | 1664-302X (online) | |
dc.identifier.other | 10.3389/fmicb.2024.1482348 | |
dc.identifier.uri | http://hdl.handle.net/2263/99737 | |
dc.language.iso | en | en_US |
dc.publisher | Frontiers Media | en_US |
dc.rights | © 2024 Maruapula, Ditshwanelo, Pema, Bareng, Choga, Moraka, Mokgethi, Seatla, Koofhethile, Zuze, Gaolathe, Pretorius-Holme, Lebani, Makhema, Novitsky, Shapiro, Lockman, Moyo and Gaseitsiwe. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). | en_US |
dc.subject | Botswana | en_US |
dc.subject | HIV drug resistance mutations | en_US |
dc.subject | SDG-03: Good health and well-being | en_US |
dc.subject | Human immunodeficiency virus (HIV) | en_US |
dc.subject | Integrase strand transfer inhibitor (INSTI) | en_US |
dc.subject | Dolutegravir (DTG) | en_US |
dc.subject | Antiretroviral therapy (ART) | en_US |
dc.title | Low prevalence of archived integrase strand transfer inhibitors resistance associated mutations in Botswana before the roll out of dolutegravir based first line antiretroviral therapy | en_US |
dc.type | Article | en_US |
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