Comparative evaluation of real-time PCR assays for detection of the human metapneumovirus

被引:87
作者
Côté, S
Abed, Y
Boivin, G
机构
[1] Ctr Hosp Univ Quebec, Infect Dis Res Ctr, CHUL, Quebec City, PQ, Canada
[2] Univ Laval, Dept Med Biol, Quebec City, PQ, Canada
关键词
D O I
10.1128/JCM.41.8.3631-3635.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 Q 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.
引用
收藏
页码:3631 / 3635
页数:5
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