HIV‑1 Genotype
Use
HIV‑1 genotype testing is used to detect drug resistance-associated mutations in relevant viral genes (reverse transcriptase and protease) to guide antiretroviral (ARV) regimen selection. It is recommended at entry into care, in pregnant individuals before therapy initiation, in those with treatment failure, or when integrase inhibitor resistance is suspected, and should be performed while on therapy or within 4 weeks of discontinuation. Mutations listed in the IAS‑USA drug resistance list (2022 or newer) are reported, including those for NRTIs, NNRTIs, and PIs. Quest uses reverse transcription, PCR amplification (RT and protease genes), and Sanger sequencing, incorporating internal rules-based interpretation informed by Stanford HIVdb.
Special Instructions
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Limitations
The test requires sufficient HIV‑1 viral load (recommended ≥500 to 1,000 copies/mL) for amplification; a result of “NOT DETECTED” may occur if viral load is insufficient, RNA degraded, or technical issues impair amplification.
Methodology
Sanger
Biomarkers
Result Turnaround Time
1-2 days
Related Documents
For more information, please review the documents below
Specimen
Plasma
Volume
Not provided
Minimum Volume
Not provided
