Simultaneous detection of parainfluenza viruses 1 and 3 by real-time reverse transcription-polymerase chain reaction

被引:12
作者
Cordeya, Samuel [1 ,2 ]
Thomas, Yves [1 ,2 ]
Cherpillod, Pascal [1 ,2 ]
van Belle, Sandra [1 ,2 ]
Tapparel, Caroline [1 ,2 ]
Kaiser, Laurent [1 ,2 ]
机构
[1] Univ Hosp Geneva, Div Infect Dis, Virol Lab, CH-1211 Geneva 14, Switzerland
[2] Univ Geneva, Sch Med, CH-1205 Geneva, Switzerland
基金
瑞士国家科学基金会;
关键词
Human parainfluenza viruses 1 and 3; Real-time RT-PCR; Diagnosis; MULTIPLEX RT-PCR; COMMON RESPIRATORY VIRUSES; CLINICAL-SAMPLES; TRANSPLANT RECIPIENTS; YOUNG-CHILDREN; RNA VIRUSES; INFECTION; TYPE-3; ASSAY; DIAGNOSIS;
D O I
10.1016/j.jviromet.2008.11.006
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Human parainfluenza virus (HPIV) types I and 3 are major viral pathogens responsible for upper and lower respiratory tract infections. The diagnosis of these two species is achieved generally by specific reverse transcription-polymerase chain (RT-PCR) reaction methods. In this study, a real-time RT-PCR was developed using a common pair of primers-probe (HPIV-1+3) for the simultaneous detection of both HPIV-1 and HPIV-3 genomes. Results obtained in a 10-fold dilution series assay demonstrate a high sensitivity of the assay with a lowest detection limit of approximately one plasmid copy for both HPIV-1 and HPIV-3. A comparison of HPIV-1 and HPIV-3 clinical sample detection between specific HPIV-1 /HPIV-3 pairs of primers-probes and the HPIV-1+3 combination clearly shows that the latter is significantly more sensitive (gain of about five threshold cycles) than the former for HPIV-3 detection, while equivalent values are observed for HPIV-1 The HPIV-1+3 combination constitutes a more rapid, more sensitive, and less expensive alternative than classical or multiplex real-time RT-PCR assays usually used in clinical laboratories. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:166 / 168
页数:3
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