HIV drug resistance profile in South Africa: Findings and implications from the 2017 national HIV household survey.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 26 05 2020
accepted: 08 10 2020
entrez: 4 11 2020
pubmed: 5 11 2020
medline: 29 12 2020
Statut: epublish

Résumé

HIV drug resistance (HIVDR) testing was included in the 2017 South African national HIV household survey. We describe the prevalence of HIVDR by drug class, age, sex and antiretroviral drugs (ARV) status. Dried blood were spots tested for HIV, with Viral load (VL), exposure to ARVs and HIVDR testing among those HIV positive. HIVDR testing was conducted on samples with VL ≥1000 copies/ml using Next Generation Sequencing. Weighted percentages of HIVDR are reported. 697/1,105 (63%) of HIV positive samples were sequenced. HIVDR was detected in samples from 200 respondents (27.4% (95% confidence interval (CI) 22.8-32.6)). Among these 130 (18.9% (95% CI 14.8-23.8)), had resistance to non-nucleoside reverse transcriptase inhibitors (NNRTIs) only, 63 (7.8% (95% CI 5.6-10.9)) resistance to NNRTIs and nucleoside reverse transcriptase inhibitors, and 3 (0.5% (95% CI 0.1-2.1)) resistance to protease inhibitors. Sixty-five (55.7% (95% CI 42.6-67.9) of ARV-positive samples had HIVDR compared to 112 (22.8% (95% CI 17.7-28.7)), in ARV-negative samples. HIVDR was found in 75.6% (95% CI 59.2-87.3), n = 27, samples from respondents who reported ARV use but tested ARV-negative, and in 15.3% (95% CI 6.3-32.8), n = 7, respondents who reported no ARV use and tested ARV-negative. There were no significant age and sex differences in HIVDR. 27% of virally unsuppressed respondents had HIVDR, increasing to 75% among those who had discontinued ARV. Our findings support strengthening first-line ARV regimens by including drugs with a higher resistance barrier and treatment adherence strategies, and close monitoring of HIVDR.

Sections du résumé

BACKGROUND
HIV drug resistance (HIVDR) testing was included in the 2017 South African national HIV household survey. We describe the prevalence of HIVDR by drug class, age, sex and antiretroviral drugs (ARV) status.
METHODS
Dried blood were spots tested for HIV, with Viral load (VL), exposure to ARVs and HIVDR testing among those HIV positive. HIVDR testing was conducted on samples with VL ≥1000 copies/ml using Next Generation Sequencing. Weighted percentages of HIVDR are reported.
RESULTS
697/1,105 (63%) of HIV positive samples were sequenced. HIVDR was detected in samples from 200 respondents (27.4% (95% confidence interval (CI) 22.8-32.6)). Among these 130 (18.9% (95% CI 14.8-23.8)), had resistance to non-nucleoside reverse transcriptase inhibitors (NNRTIs) only, 63 (7.8% (95% CI 5.6-10.9)) resistance to NNRTIs and nucleoside reverse transcriptase inhibitors, and 3 (0.5% (95% CI 0.1-2.1)) resistance to protease inhibitors. Sixty-five (55.7% (95% CI 42.6-67.9) of ARV-positive samples had HIVDR compared to 112 (22.8% (95% CI 17.7-28.7)), in ARV-negative samples. HIVDR was found in 75.6% (95% CI 59.2-87.3), n = 27, samples from respondents who reported ARV use but tested ARV-negative, and in 15.3% (95% CI 6.3-32.8), n = 7, respondents who reported no ARV use and tested ARV-negative. There were no significant age and sex differences in HIVDR.
CONCLUSION
27% of virally unsuppressed respondents had HIVDR, increasing to 75% among those who had discontinued ARV. Our findings support strengthening first-line ARV regimens by including drugs with a higher resistance barrier and treatment adherence strategies, and close monitoring of HIVDR.

Identifiants

pubmed: 33147285
doi: 10.1371/journal.pone.0241071
pii: PONE-D-20-15855
pmc: PMC7641411
doi:

Substances chimiques

Anti-HIV Agents 0

Types de publication

Journal Article Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0241071

Subventions

Organisme : PEPFAR
Pays : United States

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist

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Auteurs

Sizulu Moyo (S)

Human Sciences Research Council, Pretoria, South Africa.
School of Public Health, University of Cape Town, Cape Town, South Africa.

Gillian Hunt (G)

Centre for HIV and STIs, National Institute of Communicable Diseases, Johannesburg, South Africa.

Khangelani Zuma (K)

Human Sciences Research Council, Pretoria, South Africa.

Mpumi Zungu (M)

Human Sciences Research Council, Pretoria, South Africa.

Edmore Marinda (E)

Human Sciences Research Council, Pretoria, South Africa.
School of Public Health, University of the Witwatersrand, Johannesburg, South Africa.

Musawenkosi Mabaso (M)

Human Sciences Research Council, Pretoria, South Africa.

Vibha Kana (V)

Centre for HIV and STIs, National Institute of Communicable Diseases, Johannesburg, South Africa.

Monalisa Kalimashe (M)

Centre for HIV and STIs, National Institute of Communicable Diseases, Johannesburg, South Africa.

Johanna Ledwaba (J)

Centre for HIV and STIs, National Institute of Communicable Diseases, Johannesburg, South Africa.

Inbarani Naidoo (I)

Human Sciences Research Council, Pretoria, South Africa.

Sinovuyo Takatshana (S)

Human Sciences Research Council, Pretoria, South Africa.

Tebogo Matjokotja (T)

Human Sciences Research Council, Pretoria, South Africa.

Cheryl Dietrich (C)

Division of Global HIV and TB, Centers for Disease Control and Prevention, Pretoria, South Africa.

Elliot Raizes (E)

Division of Global HIV and TB, Centers for Disease Control and Prevention, Atlanta, GA, United States of America.

Karidia Diallo (K)

Division of Global HIV and TB, Centers for Disease Control and Prevention, Pretoria, South Africa.

Gurpreet Kindra (G)

Division of Global HIV and TB, Centers for Disease Control and Prevention, Pretoria, South Africa.

Linnetie Mugore (L)

Division of Global HIV and TB, Centers for Disease Control and Prevention, Pretoria, South Africa.

Thomas Rehle (T)

School of Public Health, University of Cape Town, Cape Town, South Africa.

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Classifications MeSH