Eldadah Z A, Asher D M, Godec M S, Pomeroy K L, Goldfarb L G, Feinstone S M, Levitan H, Gibbs C J, Gajdusek D C
Laboratory of Central Nervous System Studies, National Institute of Neurological Disorders and Stroke, Bethesda, Maryland 20892.
J Med Virol. 1991 Apr;33(4):260-7. doi: 10.1002/jmv.1890330410.
RNA sequences of five flaviviruses were detected by a modified polymerase chain reaction (PCR) that incorporated a reverse transcriptase and RNase inhibitor. Oligonucleotide primer pairs were synthesized to amplify sequences from St. Louis encephalitis (SLE), Japanese encephalitis (JBE), yellow fever (YF), dengue 2 (DEN-2), and dengue 4 (DEN-4) viruses. The amplified products were visualized as bands of appropriate size on ethidium bromide-stained agarose gels. The identity of these products was confirmed by restriction endonuclease cleavage to generate fragments of predicted lengths. The reverse-transcriptase PCR (RT-PCR) successfully amplified flavivirus sequences from cell cultures, frozen brain tissue, and formalin-fixed, paraffin-embedded brain tissue. The reactions were highly specific, and the method compared favorably to two conventional assays of viral infectivity. RT-PCR followed by PCR with nesting primers (N-PCR) was 1,000-fold more sensitive in detecting virus than classical infectivity titration by intracerebral inoculation of suckling mice and nearly 1,000-fold more sensitive than amplification of virus in cell culture followed by inoculation of mice.
通过一种改良的聚合酶链反应(PCR)检测了五种黄病毒的RNA序列,该反应加入了逆转录酶和核糖核酸酶抑制剂。合成了寡核苷酸引物对,以扩增圣路易斯脑炎(SLE)、日本脑炎(JBE)、黄热病(YF)、登革热2型(DEN-2)和登革热4型(DEN-4)病毒的序列。扩增产物在溴化乙锭染色的琼脂糖凝胶上显示为适当大小的条带。通过限制性内切酶切割产生预测长度的片段,证实了这些产物的同一性。逆转录酶PCR(RT-PCR)成功地从细胞培养物、冷冻脑组织以及福尔马林固定、石蜡包埋的脑组织中扩增出黄病毒序列。这些反应具有高度特异性,该方法与两种传统的病毒感染性检测方法相比具有优势。RT-PCR之后进行巢式引物PCR(N-PCR)在检测病毒方面比通过乳鼠脑内接种进行的经典感染性滴定敏感1000倍,比在细胞培养物中扩增病毒后接种小鼠敏感近1000倍。