Markoulatos P, Fountoucidou P, Marinakis G, Krikelis V, Spyrou N, Vamvakopoulos N, Moncany M L
Virology Department, Hellenic Pasteur Institute, Athens, Greece.
J Clin Lab Anal. 1997;11(3):146-53. doi: 10.1002/(sici)1098-2825(1997)11:3<146::aid-jcla5>3.0.co;2-8.
The severity and recurrences of Herpes Simplex Virus (HSV) infection depend on the type of the infectious agent (HSV-1 or HSV-2), which induces the necessity of a nonambiguous detecting typing. The commonly used capture ELISA technique has to be often supported by DNA analysis to confirm the detection and the typing of HSV viruses in exposed patients. In this report, we describe a rapid and cheap indirect ELISA method using anti-HSV monospecific polyclonal antibodies prepared in the laboratory. The typing of the studied samples was clear, did not need series of dilution, and allowed the immediate classification of viruses without further control examination. We tested 51 specimens, which were typed 25 HSV-1 and 26 HSV-2 strains. The comparison with capture ELISA, restriction enzyme and polymerase chain reaction analysis definitely allowed our method to be assessed as a useful tool for a routine diagnostic.
单纯疱疹病毒(HSV)感染的严重程度和复发情况取决于感染病原体的类型(HSV-1或HSV-2),这就使得明确检测分型成为必要。常用的捕获ELISA技术通常需要DNA分析来辅助,以确认暴露患者体内HSV病毒的检测和分型。在本报告中,我们描述了一种快速且廉价的间接ELISA方法,该方法使用在实验室制备的抗HSV单特异性多克隆抗体。所研究样本的分型清晰,无需系列稀释,且无需进一步的对照检查即可立即对病毒进行分类。我们检测了51个标本,其中25个为HSV-1毒株,26个为HSV-2毒株。与捕获ELISA、限制性内切酶和聚合酶链反应分析的比较明确表明,我们的方法可被评估为一种用于常规诊断的有用工具。