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TT病毒的体内和体外基因组内重排

In vivo and in vitro intragenomic rearrangement of TT viruses.

作者信息

Leppik Ludmila, Gunst Karin, Lehtinen Matti, Dillner Joakim, Streker Karin, de Villiers Ethel-Michele

机构信息

Division for the Characterization of Tumor Viruses, Deutsches Krebsforschungszentrum, Im Neuenheimer Feld 242, 69120 Heidelberg, Germany.

出版信息

J Virol. 2007 Sep;81(17):9346-56. doi: 10.1128/JVI.00781-07. Epub 2007 Jun 27.

Abstract

The in vitro replication of the Torque teno virus (TT virus) tth8 full-length genome and particle formation in a Hodgkin's lymphoma-derived cell line after transfection with cloned viral DNA were demonstrated. Analyses of the transcription patterns of tth8 and tth7 TT virus isolates in a number of lymphoma and T-cell leukemia cell lines indicated differential additional splicing events and intragenomic rearrangement generating open reading frames which could not be deducted from the genomic sequence. We also demonstrated the presence of rearranged TT virus genomes in vivo in sera taken from pregnant mothers whose children later developed childhood leukemia, as well as sera from control mothers. Control experiments using religated cloned genomic tth8 DNA mixed with cellular DNA did not result in such subviral molecules. These subviral isolates ranged from 172 bp to full-length TT virus genomes. Possible in vivo selection for specific rearranged molecules was indicated by the presence of one isolate (561 bp) in 11 serum samples. It remains to be clarified whether selected rearranged subviral components resulting from specific TT virus types may contribute to the initiation of disease. These data demonstrate new features of TT viruses suggesting possible similarities to plant viruses of the family Geminiviridae, as well as raise questions about the documented plurality and diversity of anelloviruses.

摘要

已证实转染克隆病毒DNA后,在霍奇金淋巴瘤衍生的细胞系中,丁型肝炎病毒(TT病毒)tth8全长基因组的体外复制及病毒颗粒形成。对多种淋巴瘤和T细胞白血病细胞系中tth8和tth7 TT病毒分离株转录模式的分析表明,存在差异剪接事件和基因组内重排,产生了无法从基因组序列推导出来的开放阅读框。我们还证明,在孩子后来患儿童白血病的孕妇血清以及对照母亲的血清中,体内存在重排的TT病毒基因组。使用与细胞DNA混合的重新连接的克隆基因组tth8 DNA进行的对照实验未产生此类亚病毒分子。这些亚病毒分离株的大小从172 bp到TT病毒全长基因组不等。11份血清样本中存在一种分离株(561 bp),表明可能在体内选择特定的重排分子。特定TT病毒类型产生的选定重排亚病毒成分是否可能导致疾病的发生,仍有待阐明。这些数据揭示了TT病毒的新特征,表明其可能与双生病毒科植物病毒存在相似性,同时也引发了关于环病毒已记录的多样性和差异性的问题。

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