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从艾滋病和艾滋病相关综合征(ARC)患者样本中直接检测HIV-1 RNA。

Direct detection of HIV-1 RNA from AIDS and ARC patient samples.

作者信息

Murakawa G J, Zaia J A, Spallone P A, Stephens D A, Kaplan B E, Wallace R B, Rossi J J

机构信息

Department of Microbiology, University of California, Los Angeles 90024.

出版信息

DNA. 1988 May;7(4):287-95. doi: 10.1089/dna.1988.7.287.

Abstract

Human immunodeficiency virus (HIV), formerly termed human T-lymphotropic virus (HTLVIII/LAV), is the etiological agent of acquired immune deficiency syndrome (AIDS). Direct detection of HIV-1 nucleic acid sequences in patient tissue or blood samples is possible in only a minor fraction of cases due to the low percentage of infected cells (Shaw et al., 1984). We report a modification of the polymerase chain reaction method (PCR) (Saiki et al., 1985), in which we amplify sequences from HIV-1 RNA templates, for the identification of HIV-1 in peripheral blood and tissue samples obtained from AIDS and AIDS-related complex (ARC) patients. This method of HIV-1 detection is at least six orders of magnitude more sensitive than standard nucleic acid detection methods and has direct clinical applications. In vitro tissue culturing of the virus is not required for HIV-1 detection. Using this technique, the sequence in the orfB region of HIV-1 has been amplified and detected from less than 1 microgram of total RNA prepared from a few milliliters of peripheral blood samples. This technique enables the rapid and unambiguous clinical detection of potential HIV-infected individuals and can be used to assay the efficacy of anti-HIV-1 drugs. To enhance the efficiency of this technique, we have appended the prokaryotic T7 RNA polymerase promoter sequence to one of the priming oligonucleotides. After several cycles of PCR with the promoter-containing oligo, a small aliquot of the reaction can be utilized to direct specific and efficient T7 RNA polymerase-mediated transcription of the amplified sequences, thus enhancing the sensitivity and simplifying the labor of the experiment.

摘要

人类免疫缺陷病毒(HIV),以前称为人类嗜T淋巴细胞病毒(HTLVIII/LAV),是获得性免疫缺陷综合征(AIDS)的病原体。由于受感染细胞的比例较低,仅在一小部分病例中能够直接检测患者组织或血液样本中的HIV-1核酸序列(Shaw等人,1984年)。我们报告了聚合酶链反应方法(PCR)(Saiki等人,1985年)的一种改进方法,即从HIV-1 RNA模板扩增序列,用于鉴定从艾滋病和艾滋病相关综合征(ARC)患者获得的外周血和组织样本中的HIV-1。这种HIV-1检测方法比标准核酸检测方法至少敏感六个数量级,具有直接的临床应用价值。HIV-1检测不需要对病毒进行体外组织培养。使用这种技术,已从几毫升外周血样本制备的不到1微克总RNA中扩增并检测到HIV-1的orfB区域中的序列。这项技术能够快速、明确地对潜在的HIV感染个体进行临床检测,并可用于测定抗HIV-1药物的疗效。为了提高这项技术的效率,我们在其中一个引物寡核苷酸上附加了原核T7 RNA聚合酶启动子序列。在用含启动子的寡核苷酸进行几个循环的PCR后,一小份反应产物可用于直接进行T7 RNA聚合酶介导的对扩增序列的特异性高效转录,从而提高灵敏度并简化实验操作。

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