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首页> 外文期刊>Journal of Clinical Microbiology >Impact of Human Immunodeficiency Virus Type 1 (HIV-1) Genetic Diversity on Performance of Four Commercial Viral Load Assays: LCx HIV RNA Quantitative, AMPLICOR HIV-1 MONITOR v1.5, VERSANT HIV-1 RNA 3.0, and NucliSens HIV-1 QT
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Impact of Human Immunodeficiency Virus Type 1 (HIV-1) Genetic Diversity on Performance of Four Commercial Viral Load Assays: LCx HIV RNA Quantitative, AMPLICOR HIV-1 MONITOR v1.5, VERSANT HIV-1 RNA 3.0, and NucliSens HIV-1 QT

机译:人类免疫缺陷病毒1型(HIV-1)遗传多样性对四种商业病毒载量分析性能的影响:LCx HIV RNA定量,AMPLICOR HIV-1 MONITOR v1.5,VERSANT HIV-1 RNA 3.0和NucliSens HIV-1 QT

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Human immunodeficiency virus type 1 (HIV-1) evolution and changing strain distribution present a challenge to nucleic acid-based assays. Reliable patient monitoring of viral loads requires the detection and accurate quantification of genetically diverse HIV-1. A panel of 97 HIV-1-seropositive plasma samples collected from Cameroon, Brazil, and South Africa was used to compare the performance of four commercially available HIV RNA quantitative tests: Abbott LCx HIV RNA Quantitative assay (LCx), Bayer Versant HIV-1 RNA 3.0 (bDNA), Roche AMPLICOR HIV-1 MONITOR v1.5 (Monitor v1.5), and bioMérieux NucliSens HIV-1 QT (NucliSens). The panel included group M, group O, and recombinant viruses based on sequence analysis of gag p24, pol integrase, and env gp41. The LCx HIV assay quantified viral RNA in 97 (100%) of the samples. In comparison, bDNA, Monitor v1.5, and NucliSens quantified viral RNA in 96.9%, 94.8%, and 88.6% of the samples, respectively. The two group O specimens were quantified only by the LCx HIV assay. Analysis of nucleotide mismatches at the primer/probe binding sites for Monitor v1.5, NucliSens, and LCx assays revealed that performance characteristics reflected differences in the level of genetic conservation within the target regions.
机译:人类1型免疫缺陷病毒(HIV-1)的进化和菌株分布的变化对基于核酸的检测提出了挑战。要对患者的病毒载量进行可靠的监测,需要对遗传多样的HIV-1进行检测和准确定量。从喀麦隆,巴西和南非收集的一组97个HIV-1血清阳性血浆样本用于比较四种市售的HIV RNA定量测试的性能:雅培LCx HIV RNA定量测定法(LCx),拜耳Versant HIV-1 RNA 3.0(bDNA),罗氏AMPLICOR HIV-1 MONITOR v1.5(显示器v1.5)和bioMérieuxNucliSens HIV-1 QT(NucliSens)。小组包括M组,O组和基于 gag p24, pol 整合酶和 env gp41的序列分析的重组病毒。 LCx HIV检测定量了97个样本(100%)中的病毒RNA。相比之下,bDNA,Monitor v1.5和NucliSens分别在96.9%,94.8%和88.6%的样品中定量了病毒RNA。 O组的两个标本仅通过LCx HIV分析进行定量。对Monitor v1.5,NucliSens和LCx分析的引物/探针结合位点处的核苷酸错配进行分析,发现性能特征反映了目标区域内遗传保守水平的差异。

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