Department of Experimental Immunology, Sanquin Research, Landsteiner Laboratory, Center for Infection and Immunity Amsterdam (CINIMA), Academic Medical Center of the University of Amsterdam, Amsterdam, The Netherlands.
J Virol Methods. 2010 May;165(2):311-7. doi: 10.1016/j.jviromet.2010.02.016. Epub 2010 Feb 21.
The aim of this study was to compare sensitivity thresholds of two pre-screening methods - the heteroduplex mobility assay (HMA) and the presence of ambiguity codes in population-based sequences - applied for detection of HIV-1 superinfection. HIV-1 env C2-C4 PCR products generated from 48 serum samples isolated from 24 HIV-1 positive and therapy-naïve homosexual men at seroconversion and at approximately 1 year thereafter were subjected to HMA and population sequencing. Clonal sequence analysis was used to determine the sensitivity of each method to detect sequence variability. Results from HMA were compared to pairwise genetic distance of clonal sequences; heteroduplexes resulted from as little as 1.4% pairwise distance between two sequences and were detected even when only 1.5% of the pairwise distance comparisons exceeded this distance threshold. By contrast, the ambiguity code approach using population-based sequencing detected only 20.1% of existing sequence variation and was less sensitive to minority populations <or=20%, resulting in an underestimation of HIV-1 diversity. Thus, HMA was found to be more sensitive for detection of sequence variations than the ambiguity code approach, suggesting that HMA would be a more appropriate method to pre-screen for HIV-1 superinfection.
本研究旨在比较两种预筛选方法的灵敏度阈值 - 异源双链泳动分析(HMA)和基于人群序列的模糊代码存在 - 用于检测 HIV-1 合并感染。从 24 名 HIV-1 阳性且未经治疗的同性恋男性在血清转换时和此后大约 1 年分离的 48 份血清样本中产生的 HIV-1 env C2-C4 PCR 产物,接受 HMA 和人群测序。克隆序列分析用于确定每种方法检测序列变异性的灵敏度。HMA 的结果与克隆序列的成对遗传距离进行比较;异源双链体源自两个序列之间低至 1.4%的成对距离,并且即使只有 1.5%的成对距离比较超过此距离阈值也可以检测到。相比之下,使用基于人群的测序的模糊代码方法仅检测到 20.1%的现有序列变异,并且对小于或等于 20%的少数群体的敏感性较低,导致 HIV-1 多样性的低估。因此,与模糊代码方法相比,HMA 被发现对检测序列变异更敏感,这表明 HMA 可能是一种更合适的方法来预筛选 HIV-1 合并感染。