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February 24, 20260 citationsOpen Access

Next-Generation Sequencing Reveals Continued Circulation of Rare HIV-1 Subtypes in the Democratic Republic of the Congo and Refines the Estimate of the Emergence Dates of Three Subtypes

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MAMark AndersonGOGregory S. OrfVHVera Holzmayer

Key Points

  • To assess the current diversity of HIV-1 subtypes circulating in the Democratic Republic of the Congo (DRC) and estimate the emergence dates of specific subtypes.
  • Conducted viral whole-genome sequencing on 197 specimens from 2017 to 2019.
  • Used next-generation sequencing through metagenomic and target enrichment methods.
  • Analyzed subtype diversity including unique recombinant forms and circulating recombinant forms.
  • Identified a wide variety of HIV-1 subtypes and circulating recombinant forms in the Kinshasa area.
  • Pushed back emergence dates of the most recent common ancestors of HIV-1 group M and specific rare subtypes by 3 to 7 years.
  • Confirmed ongoing circulation of rare strains that may complicate diagnostics and treatment.

Abstract

HIV-1 diversified for decades within the Democratic Republic of the Congo (DRC) before spreading globally in the early 1980s. Thus, the DRC is home to some of the most ancestral and diverse HIV-1 strains. Recent serosurveys conducted from 2017 to 2019 in Kinshasa, DRC, indicated high prevalence of HIV-1, yet sequence data is lacking from this period. Given the history of circulating rare HIV-1 subtypes in the DRC, a viral whole-genome sequencing study was conducted to determine current diversity in the greater Kinshasa area. Next-generation sequencing (NGS) through metagenomic and target enrichment methods was conducted on 197 specimens collected from 2017 to 2019. A large array of HIV subtypes (A, B, C, D, F1, G, H, J, and K), circulating recombinant forms (CRF01AE, CRF02AG, CRF05DF, CRF11cpx, CRF13cpx, CRF25cpx, CRF 45cpx, and CRF92C2U), unique recombinant forms, and unclassifiable sequences were observed, with many branching in basal positions within, or outside of, many subtypes on phylogenetic trees. Incorporating these new sequences into Bayesian inference of phylogeny pushes back the dates of the most recent common ancestors of HIV-1 group M and the rare subtypes G, H, and J by between 3 and 7 years each. The DRC continues to harbor diverse and rare HIV-1 subtypes that could challenge diagnostic tests, treatments, and vaccines. In addition to shifting subtype emergence dates, the sequences from our study are evidence that rare strains continue to circulate and should be regularly monitored.

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Cite This Study

Anderson et al. (2026) studied this question.

synapsesocial.com/papers/699d401ade8e28729cf65102https://doi.org/10.3390/v18020268
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