Côté Stéphanie, Abed Yacine, Boivin Guy
Infectious Diseases Research Center, Centre Hospitalier Universitaire de Québec (CHUQ-CHUL), Québec City, Canada.
J Clin Microbiol. 2003 Aug;41(8):3631-5. doi: 10.1128/JCM.41.8.3631-3635.2003.
The human metapneumovirus (hMPV) is a new member of the Paramyxoviridae family associated with acute respiratory tract infections in humans. The objective of this study was to compare the sensitivity of real-time RT-PCR assays performed in a LightCycler instrument and designed to amplify the viral nucleoprotein (N), matrix (M), fusion (F), phosphoprotein (P), and polymerase (L) genes. In a first evaluation of 20 viral cultures with characteristics compatible with hMPV cytopathic effect, the PCR positivity rates were 100, 90, 75, 60, and 55% using primers for the N, L, M, P, and F genes. In a second evaluation of 10 nasopharyngeal aspirates from children with bronchiolitis and found to be positive for the hMPV N gene, the PCR positivity rates for the L, M, P, and F genes were 90, 60, 30, and 80%, respectively. The analytic sensitivity of the real-time RT-PCR assay for the hMPV N gene was 100 copies using a transcribed viral plasmid. In conclusion, real-time PCR assays aimed at amplifying the N and L genes which are coding for two internal viral proteins appear particularly suitable for hMPV diagnostic.
人偏肺病毒(hMPV)是副粘病毒科的一个新成员,与人类急性呼吸道感染有关。本研究的目的是比较在LightCycler仪器中进行的、旨在扩增病毒核蛋白(N)、基质蛋白(M)、融合蛋白(F)、磷蛋白(P)和聚合酶(L)基因的实时逆转录聚合酶链反应(RT-PCR)检测方法的灵敏度。在对20份具有与hMPV细胞病变效应相符特征的病毒培养物进行的首次评估中,使用针对N、L、M、P和F基因的引物,PCR阳性率分别为100%、90%、75%、60%和55%。在对10份来自患细支气管炎且hMPV N基因检测呈阳性的儿童的鼻咽抽吸物进行的第二次评估中,L、M、P和F基因的PCR阳性率分别为90%、60%、30%和80%。使用转录的病毒质粒时,hMPV N基因实时RT-PCR检测方法的分析灵敏度为100个拷贝。总之,旨在扩增编码两种病毒内部蛋白的N和L基因的实时PCR检测方法似乎特别适合用于hMPV诊断。