Molecular confirmation of HIV-1 and HIV-2 coinfections among initially serologically dually-reactive samples from patients living in West Africa

PLoS One. 2023 Mar 31;18(3):e0283602. doi: 10.1371/journal.pone.0283602. eCollection 2023.

Abstract

Objectives: This study aimed to confirm the co-infection with HIV-1 and HIV-2, among West African patients using in-house HIV type/group enzyme-immuno assays and molecular diagnosis.

Design: A cross-sectional survey was conducted from April 2016 to October 2017 in the biggest HIV clinics of Côte d'Ivoire and Burkina Faso.

Method: A first serological confirmation was done in the referral laboratory using an in-house, indirect immuno-enzymatic essay allowing the qualitative detection of both HIV-1 and HIV-2 antibodies. In order to separately detect anti-HIV-1 and anti-HIV-2 antibodies, a type/group specific enzyme-immuno assay (HIV-GSEIA) was used. To confirm the co-infections, HIV-1 and HIV-2 DNA-qualitative PCR assays were performed.

Results: A total of 91 patients were enrolled in the study and provided blood sample for HIV type confirmatory testing including 13 (14.3%) HIV-2 mono-reactive and 78 (85.7%) HIV-1/HIV-2 dually-reactive based on the HIV testing National Algorithms. The first serological ELISA confirmatory test performed showed that 80 (78.9%) of the 91 participants were dually-reactive. The HIV-GSEIA performed on these 80 serum samples retrieve one 61 HIV-1/HIV-2 dually-reactive samples. HIV-1 and HIV-2 DNA PCR were performed on 54 of the 61 HIV-1/HIV-2 dually-reactive samples and 46 out of 61 (75.4%) samples were found HIV-1/HIV-2 coinfected.

Conclusion: The contribution of type/group specific enzyme-immuno assay to accurately identify HIV-1/HIV-2 coinfections remain suboptimal, emphasizing the need for molecular diagnosis platforms in West Africa, to avail HIV DNA PCR test for the confirmation of HIV-1/HIV-2 co-infections.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Coinfection* / diagnosis
  • Cote d'Ivoire / epidemiology
  • Cross-Sectional Studies
  • HIV Antibodies
  • HIV Infections* / complications
  • HIV Infections* / diagnosis
  • HIV Seropositivity*
  • HIV-1* / genetics
  • HIV-2 / genetics
  • Humans

Substances

  • HIV Antibodies

Grants and funding

This work was supported by The European & Developing Countries Clinical Trials Partnership (EDCTP), under the EDCTP2 Training and Mobility Action awarded to Dr BKT as Career Development Fellowship grant. [Grant number: TMA 2016 CDF 1597 EDIIMark-2; https://www.edctpgrants.org/publicportal#/search]. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. All funding sources have been reported for this study. There was no additional external funding received for this study.