A reverse transcription-nested PCR assay for HHV-6 mRNA early transcript detection after transplantation

被引:17
|
作者
Pradeau, Karine
Bordessoule, Dominique
Szelag, Jean-Christophe
Rolle, Florence
Ferrat, Pierre
Le Meur, Yann
Turlure, Pascal
Denis, Franqois
Ranger-Rogez, Sylvie [1 ]
机构
[1] CHU Dupuytren, Lab Virol, Limoges, France
[2] CHU Dupuytren, Serv Hematol Clin & Therapie Cellulaire, Limoges, France
[3] CHU Dupuytren, Serv Nephrol, Limoges, France
[4] CHU Dupuytren, Serv Chirurg Thorac & Vasc, Limoges, France
[5] Fac Pharm, Lab Microbiol, F-87025 Limoges, France
关键词
HHV-6; reactivation; U79/80; gene; mRNA detection; RT-PCR; transplant recipients;
D O I
10.1016/j.jviromet.2005.11.015
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Monitoring of human herpesvirus-6 (HHV-6) reactivation is important, especially in immunocompromised patients such as transplant recipients. Reverse transcription PCR (RT-PCR) is a useful method to distinguish between latent and active infection. Here, a RT-nested PCR coupled with a colorimetric plate hybridization assay was established to detect HHV-6 types A and B U79/80 mRNAs. After confirming the reliability of the assay on HHV-6 cultures, it was applied to the detection of HHV-6 reactivation after renal (27 patients), bone marrow (14 patients) or heart (7 patients) transplantation. A total of 206 blood samples were tested from renal (137), bone marrow (58) and heart (11) transplant recipients. U79/80 mRNAs were found in 32 samples that were considered as indicative of HHV-6 reactivation: 15, 13 and 5 from kidney, bone marrow and heart transplant recipients, respectively. Finally, U79/80 mRNA detection was correlated with clinical manifestations including leucopenia, skin rash, graft rejection or dysfunction and diarrhoea. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:41 / 47
页数:7
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