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HIV testing and quantification-1

机译:艾滋病毒检测和量化-1

摘要

There is described a method of quantifying the combined amount of an HIV-1 M group nucleic acid and an HIV-1 O group nucleic acid that may be present in a biological sample, comprising the steps of: (i) combining in a single reaction vessel said biological sample, a first amplification primer wherein said first amplification primer comprises a target hybridizing sequence consisting of SEQ ID NO: 15, a second amplification primer, and a hybridization probe; (ii) amplifying with substantially equal efficiency any of the HIV-1 M group nucleic acid and the HIV-1 O group nucleic acid present in the biological sample using an in vitro amplification reaction that comprises enzymatic extension of said first amplification primer using a first strand of said HIV-1 M group nucleic acid or said HIV-1 O group nucleic acid as a first template to create a first primer extension product, and enzymatic extension of said second amplification primer using said first primer extension product as a second template, whereby there are produced HIV-1 M group amplicons if the biological sample contained said HIV-1 M group nucleic acid, and HIV-1 O group amplicons if the biological sample contained said HIV-1 O group nucleic acid; (iii) monitoring amplicon production of said amplicons in said in vitro amplification reaction as a function of time by a process comprising detection of a signal from said hybridization probe, whereby time-dependent quantitative data is obtained; and (iv) quantifying the combined amount of said HIV-1 M group nucleic acid and said HIV-1 O group nucleic acid present in the biological sample using the time-dependent quantitative data obtained in the monitoring step, wherein neither said first amplification primer nor said second amplification primer is fully complementary to said HIV-1 M group nucleic acid or the complement thereof, or to said HIV-1 O group nucleic acid or the complement thereof, and wherein said hybridization probe hybridizes to both HIV-1 M group amplicons and HIV-1 O group amplicons.
机译:描述了定量可能存在于生物样品中的HIV-1M基团核酸和HIV-1O基团核酸的总量的方法,该方法包括以下步骤:(i)在单个反应中合并所述生物样品,第一扩增引物,其中所述第一扩增引物包含由SEQ ID NO:15组成的靶杂交序列,第二扩增引物和杂交探针; (ii)使用体外扩增反应以基本上相等的效率扩增生物样品中存在的任何HIV-1M基团核酸和HIV-1O基团核酸,所述体外扩增反应包括使用第一酶促延伸所述第一扩增引物所述HIV-1M基团核酸或所述HIV-1O基团核酸作为第一模板的链以产生第一引物延伸产物,并使用所述第一引物延伸产物作为第二模板对所述第二扩增引物进行酶促延伸,由此,如果生物样品包含所述HIV-1M基团核酸,则产生HIV-1M基团扩增子;如果生物样品包含所述HIV-1O基团核酸,则产生HIV-1O基团扩增子; (iii)通过包括检测来自所述杂交探针的信号的方法来监测所述体外扩增反应中所述扩增子的扩增产物作为时间的函数,从而获得时间依赖性的定量数据; (iv)使用在监测步骤中获得的时间依赖性定量数据,定量生物样品中存在的所述HIV-1M基团核酸和所述HIV-1O基团核酸的总量,其中所述第一扩增引物都不所述第二扩增引物也不与所述HIV-1M基团核酸或其互补序列或所述HIV-1O基团核酸或其互补序列完全互补,并且其中所述杂交探针与两个HIV-1M基团杂交扩增子和HIV-1 O组扩增子。

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