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Updated: Jan 31, 2026

Detection of Human Immunodeficiency Virus Type 1 HIV-1 Antisense Protein ASP RNA Transcripts in Patients by Strand-Specific RT-PCR
Published on: November 27, 2019
Impact of HIV type 1 subtype variation on viral RNA quantitation
B Parekh1, S Phillips, T C Granade
1Division of HIV, STD, TB Laboratory Research, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA. bsp1@cdc.gov
This study compared HIV-1 RNA viral load tests across different subtypes. The branched DNA (bDNA) assay showed better performance, especially for diverse HIV-1 strains.
Area of Science:
- Virology
- Molecular Diagnostics
- Public Health
Background:
- Accurate human immunodeficiency virus type 1 (HIV-1) RNA quantification is crucial for patient management.
- Existing viral load assays may exhibit performance variability with different HIV-1 subtypes.
Purpose of the Study:
- To evaluate and compare the performance of three HIV-1 RNA quantitation methods: Amplicor HIV-1 MONITOR-1.0, NASBA, and Quantiplex HIV RNA 2.0 (branched DNA [bDNA]).
- To assess the impact of HIV-1 subtypes (A, Thai B [B'], and E) on assay performance.
Main Methods:
- Plasma specimens (N=60) from individuals infected with HIV-1 subtypes A, B', or E (N=20 each) were analyzed.
- Performance of Amplicor HIV-1 MONITOR-1.0, NASBA, and bDNA assays was evaluated based on quantifiability and correlation.
Main Results:
- The bDNA assay demonstrated higher quantifiability for subtype A and E specimens compared to MONITOR-1.0 and NASBA.
- Subtype B' specimens showed better correlation among assays, with minor differences near the lower limit of detection.
- The enhanced MONITOR assay (MONITOR-1.0+) with a new primer set improved RNA detection across all subtypes.
Conclusions:
- HIV-1 subtype variation significantly influences viral load quantitation accuracy across different methods.
- Regular evaluation and potential modification of quantitative assays are necessary for reliable detection of diverse HIV-1 strains.
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