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使用39种M组和O组病毒的系列稀释液,将雅培实时HIV-1检测的动态范围性能与VERSANT HIV-1 RNA 3.0和AMPLICOR HIV-1 MONITOR v1.5进行比较。

Evaluation of performance across the dynamic range of the Abbott RealTime HIV-1 assay as compared to VERSANT HIV-1 RNA 3.0 and AMPLICOR HIV-1 MONITOR v1.5 using serial dilutions of 39 group M and O viruses.

作者信息

Swanson Priscilla, Huang Shihai, Abravaya Klara, de Mendoza Carmen, Soriano Vincent, Devare Sushil G, Hackett John

机构信息

Abbott Diagnostics, AIDS Research and Retrovirus Discovery, D-09NG, Bldg. AP20, 100 Abbott Park Road, Abbott Park, IL 60064-6015, USA.

出版信息

J Virol Methods. 2007 Apr;141(1):49-57. doi: 10.1016/j.jviromet.2006.11.026. Epub 2006 Dec 20.

Abstract

Performance of the Abbott m2000 instrument system and the Abbott RealTime HIV-1 assay was evaluated using a panel of 37 group M (subtypes A-D, F, G, CRF01_AE, CRF02_AG and unique recombinant forms) and 2 group O virus isolates. Testing was performed on 273 sample dilutions and compared to VERSANT HIV-1 RNA 3.0 (bDNA) and AMPLICOR HIV-1 MONITOR v1.5 (Monitor v1.5) test results. RealTime HIV-1, bDNA, and Monitor v1.5 tests quantified 87%, 78%, and 81% of samples, respectively. RealTime HIV-1 detected an additional 31 samples at < 40 copies/mL. For group M, RealTime HIV-1 dilution profiles and viral loads were highly correlated with bDNA and Monitor v1.5 values; 87% and 89% of values were within 0.5 log(10) copies/mL. In contrast, the group O viruses were not detected by Monitor v1.5 and were substantially underquantified by approximately 2 log(10) copies/mL in bDNA relative to the RealTime HIV-1 assay. Sequence analysis revealed that RealTime HIV-1 primer/probe binding sites are highly conserved and exhibit fewer nucleotide mismatches relative to Monitor v1.5. The automated m2000 system and RealTime HIV-1 assay offer the advantages of efficient sample processing and throughput with reduced "hands-on" time while providing improved sensitivity, expanded dynamic range and reliable quantification of genetically diverse HIV-1 strains.

摘要

使用一组37株M组(A - D、F、G、CRF01_AE、CRF02_AG亚型及独特重组形式)和2株O组病毒分离株,对雅培m2000仪器系统及雅培实时HIV - 1检测进行了评估。对273个样本稀释液进行检测,并与VERSANT HIV - 1 RNA 3.0(分支DNA)和AMPLICOR HIV - 1 MONITOR v1.5(监测v1.5)检测结果进行比较。实时HIV - 1、分支DNA和监测v1.5检测分别对87%、78%和81%的样本进行了定量。实时HIV - 1在<40拷贝/mL时额外检测出31个样本。对于M组,实时HIV - 1稀释曲线和病毒载量与分支DNA和监测v1.5值高度相关;87%和89%的值在0.5 log(10)拷贝/mL范围内。相比之下,监测v1.5未检测到O组病毒,且相对于实时HIV - 1检测,分支DNA对O组病毒的定量显著偏低,约低2 log(10)拷贝/mL。序列分析显示,实时HIV - 1引物/探针结合位点高度保守,相对于监测v1.5,核苷酸错配较少。自动化m2000系统和实时HIV - 1检测具有样本处理高效、通量高、“动手”时间减少的优点,同时提高了灵敏度,扩大了动态范围,并能可靠地定量基因多样的HIV - 1毒株。

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