High concordance in plasma and CSF HIV-1 drug resistance mutations despite high cases of CSF viral escape in individuals with HIV-associated cryptococcal meningitis in Botswana

Author:

Kelentse Nametso12ORCID,Moyo Sikhulile13,Choga Wonderful T1,Lechiile Kwana1,Leeme Tshepo B1,Lawrence David S14,Kasvosve Ishmael2,Musonda Rosemary13,Mosepele Mosepele15,Harrison Thomas S6,Jarvis Joseph N14,Gaseitsiwe Simani13

Affiliation:

1. Botswana Harvard AIDS Institute Partnership , Gaborone , Botswana

2. University of Botswana, Department of Medical Laboratory Sciences , Gaborone , Botswana

3. Harvard T.H. Chan School of Public Health, Department of Immunology and Infectious Diseases , Boston , USA

4. Department of Clinical Research, Faculty of Infectious and Tropical Diseases, The London School of Hygiene and Tropical Medicine , London , UK

5. University of Botswana, Department of Internal Medicine , Gaborone , Botswana

6. Centre for Global Health, Institute for Infection and Immunity, St. George’s University of London , London , UK

Abstract

AbstractObjectivesWe compared the patterns of HIV-1 drug resistance mutations between the CSF and plasma of individuals with HIV-associated cryptococcal meningitis.MethodsThis is a cross-sectional study of archived CSF and plasma samples collected from ART-exposed participants recruited in the Phase 3 AmBisome Therapy Induction Optimisation randomized controlled trial (ISRCTN72509687) conducted in Botswana between 2018 and 2021. HIV-1 RT and protease genes were genotyped using next-generation sequencing and HIV-1 drug resistance mutations were compared between the CSF and plasma compartments stratified by thresholds of ≥20% and <20%.ResultsOverall, 66.7% (16/24) of participants had at least one HIV-1 drug resistance mutation in the CSF and/or plasma. A total of 15/22 (68.2%) participants had HIV-1 drug resistance mutations at ≥20% threshold in the plasma and of those, 11 (73.3%) had been on ART longer than 6 months. HIV-1 drug resistance mutations were highly concordant between the CSF and plasma at ≥20% threshold despite a substantial number of individuals experiencing CSF viral escape and with only 54.5% with CSF WBC count ≥20 cells/mm3. Minority HIV-1 drug resistance mutations were detected in 20.8% (5/24) of participants. There were no mutations in the CSF that were not detected in the plasma.ConclusionsThere was high concordance in HIV-1 drug resistance mutations in the CSF and plasma, suggesting intercompartmental mixing and possibly a lack of compartmentalization. Some individuals harboured minority HIV-1 drug resistance mutations, demonstrating the need to employ more sensitive genotyping methods such as next-generation sequencing for the detection of low-abundance mutations.

Funder

Fogarty International Center

National Institutes of Health Common Fund

Human Health and Heredity in Africa Consortium

African Academy of Sciences

Trials of Excellence in Southern Africa

European Union

Bill & Melinda Gates Foundation

Sub-Saharan African Network for TB/HIV Research Excellence

European and Developing Countries Clinical Trials Partnership

Swedish International Development Cooperation Agency

UK Department of Health and Social Care

Foreign, Commonwealth and Development Office

UK Medical Research Council

Wellcome Trust

National Institute for Health Research

NIHR

Global Health Research Professorship to J.N.J.

NIH

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

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