Cassinotti P, Mietz H, Siegl G
Institute for Clinical Microbiology and Immunology, St. Gallen, Switzerland.
J Med Virol. 1996 Sep;50(1):75-81. doi: 10.1002/(SICI)1096-9071(199609)50:1<75::AID-JMV13>3.0.CO;2-X.
A novel multiplex nested polymerase chain reaction (PCR) assay was designed and evaluated for routine diagnosis of herpes simplex virus (HSV) infections in patients with either putative HSV infection of the central nervous system or suspected HSV keratitis. Single-tube amplification of HSV type 1 (HSV-1) or type 2 (HSV-2) DNA extracted from cerebrospinal fluid (CSF) or from keratectomy specimens was followed by differentiation of the virus type-specific PCR products either by agarose gel analysis or by DNA enzyme immunoassay. Among 417 CSF specimens obtained from 395 consecutive patients with clinically suspected HSV infection, 11 (2.6%) were positive for HSV-1 DNA and four (1.0%) probes were positive for HSV-2 DNA. None of the specimens was positive for both HSV-1 and HSV-2 DNA. The genome of HSV-2 was detected in a CSF sample obtained from a woman with meningoencephalitis and genital herpes. The presence of PCR inhibitors was detected in six of 111 (5.4%) reconstructed CSF samples. Inhibition could be removed following extraction with a commercial kit. HSV-1 DNA, but no HSV-2 DNA, was detected in corneal buttons obtained from patients with suspected herpetic keratitis. No contamination has been recorded during the 2-year routine use of this test, which has met the specific requirements of a diagnostic laboratory.
设计并评估了一种新型多重巢式聚合酶链反应(PCR)检测方法,用于对疑似中枢神经系统单纯疱疹病毒(HSV)感染或疑似HSV角膜炎患者进行HSV感染的常规诊断。从脑脊液(CSF)或角膜切除术标本中提取的1型单纯疱疹病毒(HSV-1)或2型单纯疱疹病毒(HSV-2)DNA进行单管扩增,随后通过琼脂糖凝胶分析或DNA酶免疫测定对病毒型特异性PCR产物进行鉴别。在从395例临床疑似HSV感染的连续患者中获得的417份CSF标本中,11份(2.6%)HSV-1 DNA呈阳性,4份(1.0%)探针HSV-2 DNA呈阳性。没有一份标本HSV-1和HSV-2 DNA均呈阳性。在一名患有脑膜脑炎和生殖器疱疹的女性的CSF样本中检测到了HSV-2基因组。在111份(5.4%)重建的CSF样本中有6份检测到了PCR抑制剂。使用商业试剂盒提取后可去除抑制作用。在疑似疱疹性角膜炎患者的角膜纽扣中检测到了HSV-1 DNA,但未检测到HSV-2 DNA。在该检测方法的2年常规使用过程中未记录到污染情况,该检测方法符合诊断实验室的特定要求。