Gingeras T R, Richman D D, Kwoh D Y, Guatelli J C
Salk Institute Biotechnology/Industrial Associates, Inc., La Jolla, CA 92037.
Vet Microbiol. 1990 Sep;24(3-4):235-51. doi: 10.1016/0378-1135(90)90174-t.
The capability to detect the genetic elements (DNA or RNA) of a particular pathogen as a means of identifying the infectious agent has been the traditional function of nucleic acid hybridization assays. The low copy number of genetic material from several types of viral pathogens has fostered the development of in vitro nucleic acid amplification methods as a means to increase the copy number of the characteristic genetic elements of pathogenic agents. The polymerase chain reaction (PCR) and a transcription-based amplification system (TAS) are two amplification methods that have been developed to serve this function. Both methods have been employed to study both genetic and infectious disease problems. This review discusses the characteristics of these amplification methods and describes some of their applications, especially in the study of HIV-1.
将特定病原体的遗传元件(DNA或RNA)作为识别感染因子的手段进行检测,一直是核酸杂交检测的传统功能。几种病毒病原体的遗传物质拷贝数较低,这促进了体外核酸扩增方法的发展,以此作为增加病原体特征性遗传元件拷贝数的手段。聚合酶链反应(PCR)和基于转录的扩增系统(TAS)是为实现这一功能而开发的两种扩增方法。这两种方法都已用于研究遗传和传染病问题。本文综述讨论了这些扩增方法的特点,并描述了它们的一些应用,特别是在HIV-1研究中的应用。