de Baar M P, Timmermans E C, Bakker M, de Rooij E, van Gemen B, Goudsmit J
Department of Human Retrovirology, Academic Medical Center, University of Amsterdam, Meibergdreef 15, 1105 AZ Amsterdam, The Netherlands.
J Clin Microbiol. 2001 May;39(5):1895-902. doi: 10.1128/JCM.39.5.1895-1902.2001.
To halt the human immunodeficiency virus type 1 (HIV-1) epidemic requires interventions that can prevent transmission of numerous HIV-1 subtypes. The most frequently transmitted viruses belong to the subtypes A, B, and C and the circulating recombinant forms (CRFs) AE and AG. A fast one-tube assay that identifies and distinguishes among subtypes A, B, and C and CRFs AE and AG of HIV-1 was developed. The assay amplifies a part of the gag gene sequence of the genome of all currently known HIV-1 subtypes and can identify and distinguish among the targeted subtypes as the reaction proceeds, because of the addition of subtype-specific molecular beacons with multiple fluorophores. The combination of isothermal nucleic acid sequence-based amplification and molecular beacons is a new approach in the design of real-time assays. To obtain a sufficiently specific assay, we developed a new strategy in the design of molecular beacons, purposely introducing mismatches in the molecular beacons. The subtype A and CRF AG isolates reacted with the same molecular beacon. We tested the specificity and sensitivity of the assay on a panel of the culture supernatant of 34 viruses encompassing all HIV-1 subtypes: subtypes A through G, CRF AE and AG, a group O isolate, and a group N isolate. Assay sensitivity on this panel was 92%, with 89% correct subtype identification relative to sequence analysis. A linear relationship was found between the amount of input RNA in the reaction mixture and the time that the reaction became positive. The lower detection level of the assay was approximately 10(3) copies of HIV-1 RNA per reaction. In 38% of 50 serum samples from HIV-1-infected individuals with a detectable amount of virus, we could identify subtype sequences with a specificity of 94% by using sequencing and phylogenetic analysis as the "gold standard." In conclusion, we showed the feasibility of the approach of using multiple molecular beacons labeled with different fluorophores in combination with isothermal amplification to identify and distinguish subtypes A, B, and C and CRFs AE and AG of HIV-1. Because of the low sensitivity, the assay in this format would not be suited for clinical use but can possibly be used for epidemiological monitoring as well as vaccine research studies.
要阻止人类免疫缺陷病毒1型(HIV-1)的流行,需要采取能够预防多种HIV-1亚型传播的干预措施。传播最频繁的病毒属于A、B和C亚型以及循环重组型(CRF)AE和AG。我们开发了一种快速单管检测方法,可识别和区分HIV-1的A、B、C亚型以及CRF AE和AG。该检测方法可扩增所有目前已知HIV-1亚型基因组的一部分gag基因序列,并且由于添加了带有多种荧光团的亚型特异性分子信标,在反应进行过程中能够识别和区分目标亚型。基于等温核酸序列扩增和分子信标的结合是实时检测设计中的一种新方法。为了获得足够特异的检测方法,我们在分子信标设计中开发了一种新策略,特意在分子信标中引入错配。A亚型和CRF AG分离株与相同的分子信标发生反应。我们在一组包含所有HIV-1亚型的34种病毒的培养上清液中测试了该检测方法的特异性和灵敏度:A至G亚型、CRF AE和AG、一株O组分离株和一株N组分离株。该检测方法在该组样本上的灵敏度为92%,相对于序列分析,亚型正确识别率为89%。在反应混合物中输入的RNA量与反应呈阳性的时间之间发现了线性关系。该检测方法的最低检测水平约为每个反应10(3)拷贝的HIV-1 RNA。在来自病毒载量可检测的HIV-1感染个体的50份血清样本中,38%的样本通过使用测序和系统发育分析作为“金标准”,我们能够以94%的特异性识别亚型序列。总之,我们展示了使用标记有不同荧光团的多种分子信标与等温扩增相结合的方法来识别和区分HIV-1的A、B、C亚型以及CRF AE和AG的可行性。由于灵敏度较低,这种形式的检测方法不适合临床使用,但可能可用于流行病学监测以及疫苗研究。