Development and Optimization of Oligonucleotide Ligation Assay (OLA) Probes for Detection of HIV-1 Resistance to Dolutegravir

Viruses. 2024 Jul 19;16(7):1162. doi: 10.3390/v16071162.

Abstract

The WHO currently recommends dolutegravir (DTG)-based ART for persons living with HIV infection in resource-limited-settings (RLS). To expand access to testing for HIV drug resistance (DR) to DTG in RLS, we developed probes for use in the oligonucleotide ligation assay (OLA)-Simple, a near-point of care HIV DR kit. Genotypic data from clinical trials and case reports were used to determine the mutations in HIV-1 integrase critical to identifying individuals with DTG-resistance at virologic failure of DTG-based ART. Probes to detect G118R, Q148H/K/R, N155H and R263K in HIV-1 subtypes A, B, C, D and CRF01_AE were designed using sequence alignments from the Los Alamos database and validated using 61 clinical samples of HIV-1 subtypes A, B, C, D, CRF01_AE genotyped by PacBio (n = 15) or Sanger (n = 46). Initial OLA probes failed to ligate for 16/244 (6.5%) codons (9 at G118R and 7 at Q148H/K/R). Probes revised to accommodate polymorphisms interfering with ligation at codons G118R and Q148R reduced indeterminates to 3.7% (5 at G118R and 4 at Q148H/K/R) and detected DTG-mutations with a sensitivity of 96.5% and 100% specificity. These OLA DTG resistance probes appear highly sensitive and specific across HIV-1 subtypes common in RLS with high burden of HIV infection.

Keywords: HIV-1 integrase; INSTI resistance; dolutegravir; drug resistance mutations; drug resistance testing; oligonucleotide ligation assay.

MeSH terms

  • Drug Resistance, Viral* / genetics
  • Genotype
  • Genotyping Techniques / methods
  • HIV Infections* / drug therapy
  • HIV Infections* / virology
  • HIV Integrase / genetics
  • HIV Integrase Inhibitors* / pharmacology
  • HIV Integrase Inhibitors* / therapeutic use
  • HIV-1* / drug effects
  • HIV-1* / genetics
  • HIV-1* / isolation & purification
  • Heterocyclic Compounds, 3-Ring* / pharmacology
  • Heterocyclic Compounds, 3-Ring* / therapeutic use
  • Humans
  • Mutation
  • Oligonucleotide Probes / genetics
  • Oxazines*
  • Piperazines*
  • Pyridones*

Substances

  • dolutegravir
  • Oxazines
  • Heterocyclic Compounds, 3-Ring
  • Piperazines
  • Pyridones
  • HIV Integrase Inhibitors
  • HIV Integrase
  • Oligonucleotide Probes
  • p31 integrase protein, Human immunodeficiency virus 1