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建立非致癌性小鼠γ-疱疹病毒76潜伏感染的细胞系。

Establishment of cell lines latently infected with non-oncogenic murine gammaherpesvirus 76.

作者信息

Hrabovská Z, Chalupková A, Cipková J, Mistríková J

机构信息

Department of Microbiology and Virology, Comenius University, Bratislava, Slovak Republic.

出版信息

Acta Virol. 2010;54(4):287-91. doi: 10.4149/av_2010_04_287.

Abstract

Murine gammaherpesviruses 68 (MHV-68) and 78 (MHV-78), both inducing tumors in mice and a latent infection in cells in vitro, serve as models for study of human oncogenic gammaherpesviruses, namely Epstein-Barr virus (EBV) and Kaposi's sarcoma-associated herpesvirus (KSHV). In this work, we succeeded in establishing a latent infection of HeLa and CGL1 cell lines with non-oncogenic murine gammaherpesvirus 76 (MHV-76), which differs from MHV-68 and MHV-78 besides by oncogenicity also by deletion of M1-M4 genes and eight tRNA-like sequences. Viral latency in these cell lines, λHeLa and λCGL1, was demonstrated by the presence of viral DNA, suppression of viral latency-associated ORF73 gene and appearance of low amounts of infectious virus following treatment with phorbol 12-myristate 13-acetate (PMA). Both latently infected cell lines showed irregular presence of viral antigen originating apparently from spontaneous reactivation. The growth of latently infected cells in culture was similar to that of non-infected ones. The latently-infected λHeLa cells did not induce tumors in mice following subcutaneous inoculation. These results (i) confirm that MHV-76 is the only non-oncogenic murine gammaherpesvirus of all the so far tested ones, (ii) suggest that some of the genes deleted in MHV-76 might be responsible for the oncogenicity of murine gammaherpesviruses, (iii) confirm that viral ORF73 is one of major latency-associated genes that is suppressed during virus reactivation, and (iv) present MHV-76 as another murine gammaherpesvirus useful as a model for study of gammaherpesvirus pathogenesis, oncogenicity, latency and reactivation.

摘要

小鼠γ-疱疹病毒68(MHV-68)和78(MHV-78)均可在小鼠体内诱发肿瘤,并在体外细胞中建立潜伏感染,它们可作为研究人类致癌性γ-疱疹病毒的模型,即爱泼斯坦-巴尔病毒(EBV)和卡波西肉瘤相关疱疹病毒(KSHV)。在本研究中,我们成功地用非致癌性小鼠γ-疱疹病毒76(MHV-76)建立了HeLa和CGL1细胞系的潜伏感染,该病毒与MHV-68和MHV-78不同,除致癌性外,还缺失了M1-M4基因和8个tRNA样序列。通过病毒DNA的存在、病毒潜伏相关ORF73基因的抑制以及用佛波醇12-肉豆蔻酸酯13-乙酸酯(PMA)处理后出现少量感染性病毒,证实了λHeLa和λCGL1细胞系中的病毒潜伏状态。两个潜伏感染的细胞系均显示病毒抗原的不规则存在,显然源于自发激活。潜伏感染细胞在培养中的生长与未感染细胞相似。皮下接种后,潜伏感染的λHeLa细胞在小鼠中未诱发肿瘤。这些结果(i)证实MHV-76是迄今为止所有测试的小鼠γ-疱疹病毒中唯一的非致癌性病毒,(ii)表明MHV-76中缺失的一些基因可能与小鼠γ-疱疹病毒的致癌性有关,(iii)证实病毒ORF73是病毒激活过程中被抑制的主要潜伏相关基因之一,(iv)将MHV-76作为另一种小鼠γ-疱疹病毒,可作为研究γ-疱疹病毒发病机制、致癌性、潜伏和激活的模型。

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