Detection and quantification of human metapneumovirus in pediatric specimens by real-time RT-PCR

被引:91
作者
Kuypers, J [1 ]
Wright, N [1 ]
Corey, L [1 ]
Morrow, R [1 ]
机构
[1] Univ Washington, Dept Lab Med, CHRMC, Virol Off, Seattle, WA 98105 USA
关键词
human metapneumovirus; reverse transcription-polymerase chain reaction; quantitative;
D O I
10.1016/j.jcv.2004.11.023
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Human metapneumovirus (hMPV), a recently identified virus, causes respiratory illness in children. Objectives: A real-time reverse transcription-polymerase chain reaction (RT-PCR) assay was developed and used to detect and quantify hMPV in respiratory specimens. Study design: The quantitative RT-PCR assay amplified an approximately 70 base pair fragment from the hMPV fusion protein gene. The assay was validated and used to test respiratory specimens obtained from children seen at a hospital in Seattle, Washington, from December 2002 through May 2003. Results: The assay detected 1000hMPV copies/mL of specimen, did not detect 19 other respiratory viruses, and was able to detect and accurately quantify isolates from the four known hMPV genetic lineages in a proficiency panel of 20 previously tested samples. hMPV was detected in 52 (7.2%) of 719 pediatric respiratory specimens. The mean log 10 copies/mL of hMPV in the 52 positive specimens was 7.67 (range = 4.59-10.60). Children aged 7-12 months had a significantly higher hMPV prevalence (12.4%) than did children younger than 7 months (4.7%) (P < 0.005). Children in this age group also had significantly higher levels of hMPV in their respiratory specimens (mean log 8.43 copies/mL) than did the younger children (mean log 6.93 copies/mL) (P = 0.0025). Conclusions: The rapid real-time RT-PCR assay described here is a sensitive test for clarifying the epidemiology of and diseases associated with hMPV. (C) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:299 / 305
页数:7
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