Abraham R, Chonmaitree T, McCombs J, Prabhakar B, Lo Verde P T, Ogra P L
Department of Pediatrics, University of Texas Medical Branch, Galveston 77555.
J Clin Microbiol. 1993 Feb;31(2):395-9. doi: 10.1128/jcm.31.2.395-399.1993.
This report describes a rapid method of detection of poliovirus from viral isolates of clinical specimens using a single set of primers selected from the conserved 5' noncoding region of the poliovirus genome. Of the 144 clinical viral isolates examined, 81 were positive for polioviruses and 50 were positive for nonpoliovirus enteroviruses by tissue culture neutralization and infectivity. All 81 (100%) of the viral isolates identified as poliovirus by tissue culture infectivity were also positive by polymerase chain reaction. Of 50 nonpoliovirus enterovirus isolates found to be negative for poliovirus by tissue culture neutralization and infectivity, 48 were also negative by polymerase chain reaction. The high sensitivity (100%) and specificity (96%) of the primer set indicate that this assay has potential clinical applicability in the diagnosis of nonpoliovirus enterovirus infection.
本报告描述了一种从临床标本的病毒分离物中快速检测脊髓灰质炎病毒的方法,该方法使用从脊髓灰质炎病毒基因组保守的5'非编码区中选择的一组引物。在所检测的144份临床病毒分离物中,通过组织培养中和试验和感染性检测,81份对脊髓灰质炎病毒呈阳性,50份对非脊髓灰质炎肠道病毒呈阳性。通过组织培养感染性鉴定为脊髓灰质炎病毒的所有81份(100%)病毒分离物通过聚合酶链反应也呈阳性。在通过组织培养中和试验和感染性检测发现对脊髓灰质炎病毒呈阴性的50份非脊髓灰质炎肠道病毒分离物中,48份通过聚合酶链反应也呈阴性。该引物组的高灵敏度(100%)和特异性(96%)表明该检测方法在非脊髓灰质炎肠道病毒感染的诊断中具有潜在的临床适用性。