Seattle Children's Research Institute, 1900 9th Avenue, Mailstop C9S-8, Seattle, WA 98101, USA.
J Virol Methods. 2013 Sep;192(1-2):39-43. doi: 10.1016/j.jviromet.2011.11.030. Epub 2013 May 6.
Oligonucleotide ligation assay (OLA) is a highly specific and relatively simple method to detect point mutations encoding HIV-1 drug-resistance, which can detect mutants comprising ≥2-5% of the viral population. Nevirapine (NVP), tenofovir (TDF) and lamivudine (3TC) are antiretroviral (ARV) drugs used worldwide for treatment of HIV infection and prevention of mother-to-child-transmission. Adapting the OLA to detect multiple mutations associated with HIV resistance to these ARV simultaneously would provide an efficient tool to monitor drug resistance in resource-limited settings. Known proportions of mutant and wild-type plasmids were used to optimize a multiplex OLA for detection of K103N, Y181C, K65R, and M184V in HIV subtypes B and C, and V106M and G190A in subtype C. Simultaneous detection of two mutations was impaired if probes annealed to overlapping regions of the viral template, but was sensitive to ≥2-5% when testing codons using non-overlapping probes. PCR products from HIV-subtype B- and C-infected individuals were tested by multiplex-OLA and compared to results of single-codon OLA. Multiplex-OLA detected mutations at codon pairs 103/181, 106/190 and 65/184 reliably when compared to singleplex-OLA in clinical specimens. The multiplex-OLA is sensitive and specific and reduces the cost of screening for NVP, TDF and/or 3TC resistance.
寡核苷酸连接分析(OLA)是一种高度特异和相对简单的方法,可用于检测编码 HIV-1 耐药性的点突变,该方法可检测包含≥2-5%病毒群体的突变体。奈韦拉平(NVP)、替诺福韦(TDF)和拉米夫定(3TC)是全球用于治疗 HIV 感染和预防母婴传播的抗逆转录病毒(ARV)药物。将 OLA 适应于同时检测与这些 ARV 耐药相关的多种突变,将为资源有限环境中监测耐药性提供一种有效的工具。使用已知比例的突变型和野生型质粒,优化了用于检测 HIV 亚型 B 和 C 中的 K103N、Y181C、K65R 和 M184V 以及亚型 C 中的 V106M 和 G190A 的多重 OLA。如果探针与病毒模板的重叠区域退火,则同时检测两种突变会受到损害,但当使用非重叠探针检测密码子时,其灵敏度≥2-5%。用多重-OLA 检测来自 HIV 亚型 B 和 C 感染者的 PCR 产物,并与单密码子 OLA 的结果进行比较。在临床标本中,与单重-OLA 相比,多重-OLA 可靠地检测到 103/181、106/190 和 65/184 密码子对的突变。该多重-OLA 具有敏感性和特异性,可降低 NVP、TDF 和/或 3TC 耐药性筛查的成本。