Rotbart H A
Department of Pediatrics, University of Colorado, School of Medicine, Denver 80262.
J Clin Microbiol. 1990 Mar;28(3):438-42. doi: 10.1128/jcm.28.3.438-442.1990.
Enteroviruses are among the most common causes of childhood infection. Current diagnostic techniques are often too slow and too insensitive to benefit the patient optimally. This report describes a modified polymerase chain reaction technique by which enteroviral RNA can be amplified, over a few hours, to a level detectable by agarose mini-gel electrophoresis or nucleic acid hybridization or both. Three oligomeric regions of great homology among the enteroviruses were identified and designated as a potential primer pair and probe. With this combination, all 11 of the enterovirus serotypes tested, representing the major subgroups of these pathogens, were successfully amplified and detected. The sensitivity and rapidity of this new assay speak to its potential clinical applicability in the diagnosis of enterovirus infections.
肠道病毒是儿童感染最常见的病因之一。目前的诊断技术往往过于缓慢且不够灵敏,无法为患者带来最佳益处。本报告描述了一种改良的聚合酶链反应技术,通过该技术可在数小时内将肠道病毒RNA扩增至琼脂糖微型凝胶电泳或核酸杂交或两者均可检测到的水平。在肠道病毒中鉴定出三个具有高度同源性的寡聚区域,并将其指定为潜在的引物对和探针。通过这种组合,成功扩增并检测了所测试的11种肠道病毒血清型,它们代表了这些病原体的主要亚组。这种新检测方法的灵敏度和快速性表明其在肠道病毒感染诊断中具有潜在的临床应用价值。