Swanson P, Soriano V, Devare S G, Hackett J
AIDS Research and Retrovirus Discovery, Abbott Laboratories, 100 Abbott Park Road, Abbott Park, Illinois 60064, USA.
J Clin Microbiol. 2001 Mar;39(3):862-70. doi: 10.1128/JCM.39.3.862-870.2001.
The performance of the LCx HIV RNA Quantitative (LCx HIV), AMPLICOR HIV-1 MONITOR version 1.5 (MONITOR v1.5), and Quantiplex HIV-1 RNA version 3.0 (bDNA v3.0) viral load assays was evaluated with 39 viral isolates (3 A, 7 B, 6 C, 4 D, 8 E, 4 F, 1 G, 4 mosaic, and 2 group O). Quantitation across the assay dynamic ranges was assessed using serial fivefold dilutions of the viruses. In addition, sequences of gag-encoded p24 (gag p24), pol-encoded integrase, and env-encoded gp41 were analyzed to assign group and subtype and to assess nucleotide mismatches at primer and probe binding sites. For group M isolates, quantification was highly correlated among all three assays. In contrast, only the LCx HIV assay reliably quantified group O isolates. The bDNA v3.0 assay detected but consistently underquantified group O viruses, whereas the MONITOR v1.5 test failed to detect group O viruses. Analysis of target regions revealed fewer primer or probe mismatches in the LCx HIV assay than in the MONITOR v1.5 test. Consistent with the high level of nucleotide conservation is the ability of the LCx HIV assay to quantify efficiently human immunodeficiency virus type 1 group M and the genetically diverse group O.
使用39种病毒分离株(3种A亚型、7种B亚型、6种C亚型、4种D亚型、8种E亚型、4种F亚型、1种G亚型、4种嵌合型和2种O组)评估了LCx HIV RNA定量检测法(LCx HIV)、AMPLICOR HIV-1 MONITOR 1.5版(MONITOR v1.5)和Quantiplex HIV-1 RNA 3.0版(bDNA v3.0)的病毒载量检测性能。通过对病毒进行连续五倍稀释来评估各检测方法动态范围内的定量情况。此外,还分析了gag编码的p24(gag p24)、pol编码的整合酶和env编码的gp41的序列,以确定组和亚型,并评估引物和探针结合位点的核苷酸错配情况。对于M组分离株,所有三种检测方法的定量结果高度相关。相比之下,只有LCx HIV检测法能够可靠地对O组分离株进行定量。bDNA v3.0检测法能检测到O组病毒,但始终对其定量不足,而MONITOR v1.5检测法未能检测到O组病毒。对靶区域的分析显示,LCx HIV检测法中引物或探针错配比MONITOR v1.5检测法少。与高度的核苷酸保守性一致的是,LCx HIV检测法能够有效地对1型人类免疫缺陷病毒M组和基因多样的O组进行定量。