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Development and Optimization of Oligonucleotide Ligation Assay (OLA) Probes for Detection of HIV-1 Resistance to Dolutegravir.
Beck, Ingrid A; Boyce, Ceejay L; Bishop, Marley D; Vu, Yen L; Fung, Amanda; Styrchak, Sheila; Panpradist, Nuttada; Lutz, Barry R; Frenkel, Lisa M.
Affiliation
  • Beck IA; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
  • Boyce CL; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
  • Bishop MD; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
  • Vu YL; Department of Bioengineering, University of Washington, Seattle, WA 98195, USA.
  • Fung A; Department of Bioengineering, University of Washington, Seattle, WA 98195, USA.
  • Styrchak S; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
  • Panpradist N; Department of Bioengineering, University of Washington, Seattle, WA 98195, USA.
  • Lutz BR; Department of Bioengineering, University of Washington, Seattle, WA 98195, USA.
  • Frenkel LM; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA 98109, USA.
Viruses ; 16(7)2024 Jul 19.
Article in En | MEDLINE | ID: mdl-39066324
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oxazines / Piperazines / Pyridones / HIV Infections / HIV-1 / HIV Integrase Inhibitors / Drug Resistance, Viral / Heterocyclic Compounds, 3-Ring Limits: Humans Language: En Journal: Viruses Year: 2024 Document type: Article Affiliation country: Estados Unidos Country of publication: Suiza

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oxazines / Piperazines / Pyridones / HIV Infections / HIV-1 / HIV Integrase Inhibitors / Drug Resistance, Viral / Heterocyclic Compounds, 3-Ring Limits: Humans Language: En Journal: Viruses Year: 2024 Document type: Article Affiliation country: Estados Unidos Country of publication: Suiza