Gama R E, Horsnell P R, Hughes P J, North C, Bruce C B, al-Nakib W, Stanway G
Department of Biology, University of Essex, Colchester, England.
J Med Virol. 1989 Jun;28(2):73-7. doi: 10.1002/jmv.1890280204.
We describe a novel method for the detection of human rhinoviruses in clinical samples, using the polymerase chain reaction. Two synthetic oligonucleotide primers were produced that bind in the 5' noncoding region of all rhinovirus serotypes tested, about 350 nucleotides apart, and were used to prime polymerase chain reaction amplification of the intervening stretch of DNA. The product of this reaction, which can be clearly visualized by gel electrophoresis, is a discrete 380 bp band, the occurrence of which is diagnostic of the presence of a rhinovirus in the clinical sample analysed. The technique, which is rapid, sensitive, and reliable, has been used successfully for all the different rhinovirus serotypes tested to date in our laboratory. However, the sensitivity of detection is greatly dependent on the inclusion of both tRNA and vanadyl complexes during the viral RNA extraction process. Using this technique, under optimal conditions, we were able to detect virus in clinical samples with titres as low as TCID50 10(2.5).
我们描述了一种利用聚合酶链反应在临床样本中检测人鼻病毒的新方法。制备了两种合成寡核苷酸引物,它们结合在所有测试鼻病毒血清型的5'非编码区,相距约350个核苷酸,并用于引发中间DNA片段的聚合酶链反应扩增。该反应的产物可通过凝胶电泳清晰地观察到,是一条离散的380 bp条带,其出现可诊断所分析临床样本中存在鼻病毒。该技术快速、灵敏且可靠,已成功应用于我们实验室迄今为止测试的所有不同鼻病毒血清型。然而,检测的灵敏度在很大程度上取决于病毒RNA提取过程中同时加入tRNA和钒基复合物。在最佳条件下,使用该技术我们能够在临床样本中检测到低至TCID50 10(2.5)滴度的病毒。