Development of a quantitative TaqMan RT-PCR for respiratory syncytial virus

被引:30
作者
Dewhurst-Maridor, G
Simonet, V
Bornand, JE
Nicod, LP
Pache, JC
机构
[1] CMU, Div Clin Pathol, CH-1211 Geneva 4, Switzerland
[2] Univ Hosp Geneva, Virol Lab, CH-1205 Geneva, Switzerland
[3] Univ Hosp Geneva, Div Pulm, CH-1205 Geneva, Switzerland
关键词
respiratory syncytial virus (RSV); quantitative RT-PCR; TaqMan; SYBR green; immunocompromised patients;
D O I
10.1016/j.jviromet.2004.03.017
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Respiratory syncytial virus (RSV) is a ubiquitous RNA virus of the family Paramyxoviridae that may interfere with graft tolerance and with other interstitial lung diseases. The low viral titre observed in the immunodeficient transplanted patients requires a highly sensitive detection method. Although different tests already exist for the detection of RSV, reverse transcription-polymerase chain reaction (RT-PCR) has been shown to have the best sensitivity. In this study, a SYBR Green assay was established for the detection of RSV A and RSV B in a common screening test, and two quantitative TaqMan RT-PCRs were developed to quantify both RSV subgroups separately. Standard dilutions obtained from RSV cell infections were included in each test, and the assay was normalised using a housekeeping gene. RSV was found in 16% of the transplanted patients tested. The quantitative TaqMan assay is fast, reproducible, specific and very sensitive, and could facilitate considerably the detection of RSV virus. This would in-turn facilitate studies on the role of RSV in graft rejection. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:41 / 49
页数:9
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