Delecluse H J, Schüller S, Hammerschmidt W
Institut für Klinische Molekularbiologie und Tumorgenetik, GSF-Forschungszentrum für Umwelt und Gesundheit, GmbH, München, Germany.
EMBO J. 1993 Aug;12(8):3277-86. doi: 10.1002/j.1460-2075.1993.tb05997.x.
Marek's disease virus (MDV), a lymphotropic herpesvirus, induces T-cell lymphomas in chicken, its natural host. The lymphoma cells are latently infected with MDV but the viral contribution to the transformed phenotype is not understood. To investigate the virus-cell interaction, we focused on the status of MDV in the transformed cells. By the use of highly sensitive fluorescent in situ hybridization with metaphase chromosomes, we found (i) MDV DNA to be randomly integrated at multiple sites in the chromosomes of primary lymphoma cells from chicken tissues; (ii) extrachromosomal, circular MDV genomes were absent and linear virion DNA was usually not detectable in the latently infected lymphoma cells; (iii) the pattern of integration sites revealed the clonal origin of the tumour cells; which (iv) was retained in in vitro established cell lines derived from primary lymphomas; (v) activation of the lytic phase of MDV's life cycle occurred in vitro suggesting that MDV can escape from its integrated status by an unknown mechanism.
马立克氏病病毒(MDV)是一种嗜淋巴细胞性疱疹病毒,可在其天然宿主鸡体内诱发T细胞淋巴瘤。淋巴瘤细胞被MDV潜伏感染,但病毒对转化表型的作用尚不清楚。为了研究病毒与细胞的相互作用,我们重点关注了MDV在转化细胞中的状态。通过使用对中期染色体高度敏感的荧光原位杂交技术,我们发现:(i)MDV DNA随机整合到来自鸡组织的原发性淋巴瘤细胞染色体的多个位点;(ii)在潜伏感染的淋巴瘤细胞中不存在染色体外环状MDV基因组,且通常检测不到线性病毒粒子DNA;(iii)整合位点模式揭示了肿瘤细胞的克隆起源;(iv)在源自原发性淋巴瘤的体外建立的细胞系中得以保留;(v)MDV生命周期裂解期的激活在体外发生,这表明MDV可通过未知机制从其整合状态中逃逸。