P. Swanson et al., Quantification of HIV-1 group M (subtypes A-G) and group O by the LCx HIV RNA quantitative assay, J VIROL MET, 89(1-2), 2000, pp. 97-108
Human immunodeficiency virus type 1 (HIV-1) genetic diversity presents a ch
allenge to nucleic acid-based assays with regard to sensitivity of detectio
n and accuracy of quantification. The Abbott LCx HIV RNA Quantitative assay
(LCx(R) HIV assay), a competitive RT-PCR targeting the pol integrase regio
n, was evaluated using a panel of 297 HIV-1 seropositive plasma samples fro
m Cameroon, Uganda, Brazil, Thailand, Spain, Argentina and South Africa. Th
e panel included group M subtypes A-G, mosaics, and group O based on sequen
ce analysis of gag p24, pol integrase, and env gp41. The LCx HIV assay quan
tified 290 (97.6%) of the samples, including all the group O samples tested
. In comparison, the Roche AMPLICOR HIV-1 MONITOR test versions 1.0 and 1.5
quantified 67.3 and 94.6% of the samples, respectively. No group O specime
ns were quantified by either version of AMPLICOR HIV-1 MONITOR. Seven speci
mens were below the detectable limits of all the three assays. The LCx HIV
assay had fewer nucleotide mismatches at primer/probe binding sites as comp
ared with both AMPLICOR HIV-1 MONITOR tests. The high degree of nucleotide
conservation within the pol target region enables the LCx HIV assay to effi
ciently quantify the HIV-1 subtypes A-G and the most genetically diverse HI
V-1, group O. (C) 2000 Elsevier Science B.V. All rights reserved.