Simultaneous detection of human bocavirus and adenovirus by multiplex real-time PCR in a Belgian paediatric population

被引:24
作者
De Vos, N. [1 ]
Vankeerberghen, A. [1 ]
Vaeyens, F. [1 ]
Van Vaerenbergh, K. [1 ]
Boel, A. [1 ]
De Beenhouwer, H. [1 ]
机构
[1] Onze Lieve Vrouw Hosp, Dept Microbiol & Mol Biol, Lab Clin Biol, B-9300 Aalst, Belgium
关键词
RESPIRATORY-TRACT INFECTIONS; CHILDREN; VIRUS; PARVOVIRUS; DNA; ASSAYS;
D O I
10.1007/s10096-009-0780-y
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Since the discovery of human bocavirus (hBoV), the virus has been detected worldwide in respiratory tract samples from young children by various polymerase chain reaction (PCR) assays and real-time PCRs (Q-PCR). Until now, no data have been reported on the presence of hBoV in Belgium and the detection of hBoV in a multiplex Q-PCR setting has not been described. The aim of this study was to develop a fast and reliable multiplex Q-PCR for the simultaneous detection of hBoV DNA and adenovirus (AdV) DNA. During the winter of 2004-2005, 445 nasopharyngeal aspirates (NPAs) were analysed from 404 Belgian children up to 5 years old with acute respiratory tract infections (ARTIs). (Co)infections with hBoV, AdV, respiratory syncytial virus (RSV), human metapneumovirus (hMPV) and influenza A virus were investigated. A viral agent was detected in 61% (n = 272/445) of the NPAs. Multiplex Q-PCR found a prevalence of 11% (n = 51/445) hBoV and 13% (n = 58/445) AdV. Coinfections were more frequently found with AdV (62%; n = 36/58) than with hBoV (49%; n = 25/51). Follow-up samples were available from 22 patients with ARTIs. In three patients, hBoV DNA persisted for one month. Multiplex Q-PCR may help in closing the diagnostic gap by addressing a broader range of potential respiratory pathogens.
引用
收藏
页码:1305 / 1310
页数:6
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