Performance of the Applied Biosystems HIV-1 Genotyping Kit with Integrase

Author:

Moore Hannah P.1ORCID,Palumbo Philip J.1,Notarte Kin Israel1,Fogel Jessica M.1,Cummings Vanessa1,Gamble Theresa2,Del Rio Carlos3,Batey D. Scott4,Mayer Kenneth H.56,Farley Jason E.7,Remien Robert H.89,Beyrer Chris10,Hudelson Sarah E.1,Eshleman Susan H.1ORCID,

Affiliation:

1. Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA

2. FHI 360, Durham, North Carolina, USA

3. Department of Medicine, Emory University School of Medicine, Atlanta, Georgia, USA

4. School of Social Work, Tulane Universtiy, New Orleans, Louisiana, USA

5. Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA

6. Fenway Institute, Boston, Massachusetts, USA

7. The Center for Infectious Disease and Nursing Innovation, Johns Hopkins University School of Nursing, Baltimore, Maryland, USA

8. HIV Center for Clinical and Behavioral Studies, New York State Psychiatric Institute, New York, New York, USA

9. Department of Psychiatry, Columbia University, New York, New York, USA

10. Global Health Institute, Duke University, Durham, North Carolina, USA

Abstract

ABSTRACT HIV genotyping is used to assess HIV susceptibility to antiretroviral drugs. The Applied Biosystems HIV-1 Genotyping Kit with Integrase (AB kit, Thermo Fisher Scientific) detects resistance-associated mutations (RAMs) in HIV protease (PR), reverse transcriptase (RT), and integrase (IN). We compared results from the AB kit with results obtained previously with the ViroSeq HIV-1 Genotyping System. DNA amplicons from the AB kit were also analyzed using next-generation sequencing (NGS). HIV RNA was extracted using the MagNA Pure 24 instrument (Roche Diagnostics; 96 plasma samples, HIV subtype B, viral load range: 530–737,741 copies/mL). FASTA files were generated from AB kit data using Exatype (Hyrax Biosciences). DNA amplicons from the AB kit were also analyzed by NGS using the Nextera XT kit (Illumina). Drug resistance was predicted using the Stanford HIV Drug Resistance Database. The mean genetic distance for sequences from ViroSeq and the AB kit was 0.02% for PR/RT and 0.04% for IN; 103 major RAMs were detected by both methods. Four additional major RAMs were detected by the AB kit only. These four major RAMs were also detected by NGS (detected in 18.1%–38.2% of NGS reads). NGS detected 27 major RAMs that were not detected with either of the Sanger sequencing-based kits. All major RAMs detected with ViroSeq were detected with the AB kit; additional RAMs were detected with the AB kit only. DNA amplicons from the AB kit can be used for NGS for more sensitive detection of RAMs.

Funder

National Institutes of Health

Publisher

American Society for Microbiology

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