Evidence map›Paper›PMID 42432698›Full record

ArticleVirology journal2026

Major protease inhibitor drug resistance mutations among patients with virological failure on second-line antiretroviral therapy in Zimbabwe: a retrospective cross-sectional study.

Justin Mayini, Tendai Washaya, Justen Manasa, Edward Zumbika, Shungu Munyati, Ryman Shoko, Christine Dahlke, Vinie Kouamou

Abstract read
In one paragraph

Article in Virology journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Justin MayiniBiomedical Research and Training Institute, 10 Seagrave Road, Avondale Harare, Avondale, Harare, Zimbabwe. jmayini@brti.co.zw.ORCID https://orcid.org/0000-0002-5966-3103
Tendai WashayaBiomedical Research and Training Institute, 10 Seagrave Road, Avondale Harare, Avondale, Harare, Zimbabwe.
Justen ManasaBiomedical Research and Training Institute, 10 Seagrave Road, Avondale Harare, Avondale, Harare, Zimbabwe.
Edward ZumbikaNational University of Science and Technology, Bulawayo, Zimbabwe.
Shungu MunyatiBiomedical Research and Training Institute, 10 Seagrave Road, Avondale Harare, Avondale, Harare, Zimbabwe.
Ryman ShokoSchool of Medicine and Health Sciences, University of Lusaka, Lusaka, Zambia.
Christine DahlkeInstitute for Infection Research and Vaccine Development, Hamburg, Germany.
Vinie KouamouLaboratory of immunoregulation and infectious Diseases, NIAID, NIH Clinical Center, Bethesda, USA.

Funding

Advanced Training in Community Based Research; training in Bio-informatics, Drug Resistance and PathogenesisD43TW011326 · FIC · BIOMEDICAL RESEARCH & TRAINING INSTITUTE · PI MUNYATI, SHUNGU · 2020 to 2024
$1.6M
FIC NIH HHS D43 TW011326Fogarty International Centre of the National Institutes of Health D43 TW011326
6 · The paper itself

Abstract

backgroundVirological failure (VF) on protease inhibitor (PI)-based second-line antiretroviral therapy (ART) remains an important driver of HIV drug resistance (HIVDR) in sub-Saharan Africa. Despite widespread adoption of dolutegravir (DTG)-based first-line ART, many people living with HIV (PLWH) remain on PI-based second-line regimens. Data on major PI drug resistance mutations (DRMs) in Zimbabwe remain limited.

methodsWe conducted a retrospective cross-sectional study of archived plasma specimens from PLWH with VF (viral load (VL) ≥ 1,000 copies/mL) receiving PI-based second-line ART in Zimbabwe between January 2021 and June 2025. HIV-1 protease and reverse transcriptase regions were Sanger-sequenced, and resistance was interpreted using the Stanford HIV Drug Resistance Database. Factors associated with major PI DRMs were evaluated using multivariable logistic regression.

resultsAmong 297 participants, 153 (51.5%, 95% confidence interval [CI] 45.8-57.2%) harboured major PI DRMs. The most frequent mutations were M46I (22.6%), V82A (19.2%), and I54V (17.2%). NRTI- and NNRTI-associated DRMs were present in 70.4% and 79.5% of participants, respectively, while 47.8% exhibited triple-class resistance. Predicted susceptibility to darunavir/ritonavir remained high (78.8%), despite resistance to atazanavir/ritonavir (45.5%) and lopinavir/ritonavir (50.8%). In multivariable analysis, increasing age (adjusted odds ratio [aOR] 1.04, P < 0.001), higher VL (aOR 1.55, P = 0.011) and male sex (aOR 1.59, P = 0.044) were independently associated with major PI DRMs.

conclusionsMajor PI DRMs and multiclass HIVDR were common among PLWH with VF on PI-based second-line ART. Routine VL monitoring and early resistance testing are needed to detect and guide second-line ART failure in Zimbabwe.

Indexed as

Drug Resistance, ViralHIV-1HIV InfectionsHIV Protease InhibitorsMutationAdultCross-Sectional StudiesFemaleHIV ProteaseHumansMaleMiddle AgedRetrospective StudiesTreatment FailureViral LoadZimbabweHIV ProteaseHIV Protease InhibitorsDrug Resistance MutationsHIV-1 Subtype CProtease InhibitorsVirological FailureZimbabwe

Identifiers

PMID42432698
PMCPMC13647759

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.