Bergallo Massimiliano, Costa Cristina, Baro Sara, Musso Tiziana, Balbo Luciano, Merlino Chiara, Cavallo Rossana
Department of Public Health and Microbiology, Virology Unit, University of Turin, Via Santena 9, 10126 Torino, Italy.
J Biotechnol. 2007 Feb 20;128(3):462-76. doi: 10.1016/j.jbiotec.2006.11.005. Epub 2006 Nov 17.
This paper describes the development of two multiplex-nested RT-PCR devised to evaluate latent/immortalizing (EBNA1, EBNA2, LMP1 and LMP2) and lytic [immediate early (Zebra), early, and late (VCA), respectively] Epstein Barr virus (EBV) transcripts. Subsequently, the assays have been validated evaluating the EBV latent/lytic gene expression in peripheral blood mononuclear cells (PBMC) from immunocompetent subjects (children with primary EBV infection, past EBV infection and no EBV infection) and from immunosuppressed patients (30 asymptomatic renal transplant recipients and 4 liver transplant patients with diagnosed post-transplant lymphoproliferative disorders [PTLD]). Our two multiplex-nested RT-PCR assays provide a reliable, rapid and sensitive system, enabling the simultaneous detection and identification of seven latent/immortalizing and lytic EBV transcripts. These assays could be employed in further investigations in order to evaluate the EBV transcriptional profile in EBV-related diseases both in immunocompetent and immunocompromised hosts.
本文描述了两种多重巢式逆转录聚合酶链反应(RT-PCR)的开发,旨在评估潜伏/永生化(EBNA1、EBNA2、LMP1和LMP2)和裂解[分别为立即早期(Zebra)、早期和晚期(VCA)]爱泼斯坦-巴尔病毒(EBV)转录本。随后,通过评估免疫功能正常的受试者(原发性EBV感染儿童、既往EBV感染儿童和未感染EBV儿童)以及免疫抑制患者(30例无症状肾移植受者和4例诊断为移植后淋巴细胞增殖性疾病[PTLD]的肝移植患者)外周血单个核细胞(PBMC)中的EBV潜伏/裂解基因表达,对这些检测方法进行了验证。我们的两种多重巢式RT-PCR检测方法提供了一个可靠、快速且灵敏的系统,能够同时检测和鉴定七种潜伏/永生化和裂解性EBV转录本。这些检测方法可用于进一步研究,以评估免疫功能正常和免疫功能低下宿主中EBV相关疾病的EBV转录谱。