Rapier J M, Villamarzo Y, Schochetman G, Ou C Y, Brakel C L, Donegan J, Maltzman W, Lee S, Kirtikar D, Gatica D
Division of HIV/AIDS, Centers for Disease Control, Atlanta, GA 30333.
Clin Chem. 1993 Feb;39(2):244-7.
A nonradioactive, colorimetric microplate hybridization procedure was used to assay human immunodeficiency virus (HIV) DNA, amplified by the polymerase chain reaction (PCR). Under the PCR conditions used, four proviral copies per 150,000 cells were detected by amplifying a series of DNA mixtures that contained various copy numbers of HIV. Assays of PCR-amplified DNA from peripheral blood mononuclear cells of seronegative individuals yielded negative results (104 of 104), whereas samples from seropositive individuals yielded > 99% positive results (141 of 142). Similar results were obtained in a chemiluminescent assay with an acridinium ester-labeled probe and in a solution hybridization assay in which a 32P-labeled probe was used.
采用一种非放射性的比色微孔板杂交程序来检测经聚合酶链反应(PCR)扩增的人类免疫缺陷病毒(HIV)DNA。在所使用的PCR条件下,通过扩增一系列含有不同拷贝数HIV的DNA混合物,可检测到每150,000个细胞中有四个前病毒拷贝。对血清阴性个体外周血单个核细胞的PCR扩增DNA进行检测,结果均为阴性(104例检测中104例阴性),而血清阳性个体的样本检测结果阳性率>99%(142例检测中141例阳性)。使用吖啶酯标记探针的化学发光检测以及使用32P标记探针的溶液杂交检测也获得了类似结果。