Fernandez-Muñoz R, Celma M L
Unidad de Virología, Hospital Ramón y Cajal, Madrid, Spain.
J Gen Virol. 1992 Sep;73 ( Pt 9):2195-202. doi: 10.1099/0022-1317-73-9-2195.
To investigate the mechanisms of measles virus (MV) establishment and maintenance of persistence in lymphoid cells, we have established a long-term persistent infection with MV, Edmonston strain, in the human T lymphoblastoid cell line MOLT4, which has been in continuous culture for over 8 years. In this culture, designated MOMP1, more than 98% of cells display viral antigens. The MOMP1 culture is immune to superinfection with MV and is not cured by anti-MV antibodies. No evidence of defective interfering particles was obtained. The persistently infected culture releases an infectious virus showing a miniplaque and thermoresistant modified phenotype that, unlike the parental virus Edmonston strain which produces a lytic infection with extensive cell fusion, establishes an immediate persistence in MOLT4 cells with neither significant loss of cell viability nor cell fusion. This suggests that the modification in the virus suffices to maintain the state of persistence without requiring a coevolution of the host cell during the infection, as has been reported in other persistent virus infections.
为了研究麻疹病毒(MV)在淋巴细胞中建立和维持持续性感染的机制,我们在人T淋巴母细胞系MOLT4中建立了Edmonston株MV的长期持续性感染,该细胞系已连续培养超过8年。在这种命名为MOMP1的培养物中,超过98%的细胞显示出病毒抗原。MOMP1培养物对MV的超感染具有免疫力,并且不能被抗MV抗体治愈。未获得缺陷干扰颗粒的证据。持续感染的培养物释放出一种具有小蚀斑和耐热修饰表型的感染性病毒,与产生广泛细胞融合的裂解性感染的亲本病毒Edmonston株不同,它在MOLT4细胞中立即建立持续性感染,细胞活力没有明显损失,也没有细胞融合。这表明病毒的修饰足以维持持续性状态,而不需要宿主细胞在感染过程中共同进化,这与其他持续性病毒感染的报道一致。