Risatti G, Holinka L, Lu Z, Kutish G, Callahan J D, Nelson W M, Brea Tió E, Borca M V
Plum Island Animal Disease Center, Agricultual Research Service, United States Department of Agriculture, P.O. Box 848, Greenport, NY 11944-0848, USA.
J Clin Microbiol. 2005 Jan;43(1):468-71. doi: 10.1128/JCM.43.1.468-471.2005.
A fluorogenic-probe hydrolysis (TaqMan)-reverse transcriptase (RT) PCR for classical swine fever virus (CSFV) was evaluated for diagnostic sensitivity and specificity by using clinical samples obtained from the Dominican Republic, where the disease is enzootic. The sensitivity of this test, using nasal swab samples taken from both symptomatic and asymptomatic animals, exceeded the diagnostic sensitivity of virus isolation (100% versus 72.4%, respectively) with little loss of specificity (98.9% versus 100%, respectively). At the herd level, three of four infected farms were identified by virus isolation, while the CSFV real-time RT-PCR assay identified all four infected premises. This simple and accurate test permits rapid detection of CSFV in affected herds.
利用从猪瘟呈地方流行的多米尼加共和国采集的临床样本,对一种用于检测经典猪瘟病毒(CSFV)的荧光探针水解(TaqMan)逆转录酶(RT)PCR方法的诊断敏感性和特异性进行了评估。该检测方法使用从有症状和无症状动物采集的鼻拭子样本,其敏感性超过了病毒分离法的诊断敏感性(分别为100%和72.4%),而特异性仅有少量损失(分别为98.9%和100%)。在畜群层面,病毒分离法识别出了四个受感染农场中的三个,而CSFV实时RT-PCR检测法识别出了所有四个受感染场所。这种简单而准确的检测方法能够快速检测出受感染畜群中的CSFV。