Table 4.: Target Genomic Region, Characteristics of the Internal Control, Amplification and Detection Strategies, Results Reports, Decontamination System, Dynamic Range, Specificity and Subtype Detection Features Provided by the Main Manufacturers of Commercial Viral Load Assays

Abbott RealTime HIV-1 (m2000rt) COBAS® AmpliPrep/COBAS® TaqMan HIV-1, v2.0 (Roche) NucliSens® EasyQ HIV-1 v1.2 (bioMérieux) VERSANT® HIV-1 RNA 1.0 (kPCR) (Siemens) Artus HI Virus-1 QS-RGQ (Qiagen)
HIV target region Highly conserved region within the pol gene (integrase) Dual target: highly conserved region of the gag gene (p41) and LTR Highly conserved region within the gag gene (p24) Highly conserved region within the pol gene (integrase) 5LTR region
Internal control Yes. Non-competitive Yes Yes. Non-competitive Yes Yes
Amplification Real-time PCR Real-time PCR (TaqMan) Real-time PCR (NASBA) Real-time PCR (TaqMan) Real-time PCR
Detection Fluorescence Fluorescence Fluorescence - Molecular beacons Fluorescence Fluorescence
Quantification Copies/ml, log10 copies/ml, IU/ml or log10 IU/ml; conversion factor to IU/ml is 1 IU=0.56 copies and 1 copy=1.74 IU Copies/ml, log10 copies/ml; conversion factor to IU/ml is 1 IU=0.6 copies and 1 copy=1.7 IU Copies/ml; conversion to IU 1:1 Copies/ml; IU/ml UI/ml; conversion factor 1 IU=0.46 copies and 1 copy=2.17 IU
Linear dynamic range 40 copies/ml from 600 l
11 million copies/ml
20 copies/ml from 850 l
10 million copies/ml
24 copies/ml
1 million copies/ml
37 copies/ml
11 million copies/ml
112.5 copies/ml
45 million copies/ml
Specificity (%) (95%) 100 (99.28-100) 100 (99.3-100) 100 99.7 (99.3-100) 100
Subtypes/HIV-2 Group M -subtypes A-D, F-H, various CRFs, including CRF01_AE and CRF02_AG; group N, O and P.
Does not detect HIV-2.
Group M -subtypes A-D, F-H, various CRFs, including CRF01_AE; group O
Does not detect HIV-2.
Group M -subtypes A-D, F-H, J
Does not detect HIV-2.
Group M -subtypes A-D, F-H, CRF01_AE and CRF02_AG; group O
Does not detect HIV-2.
Group M -subtypes A-D, F-H
Does not detect HIV-2.
Control of contamination with AmpErase No AmpErase (UNG) No AmpErase (UNG) No