Harada S, Koyanagi Y, Yamamoto N
Virology. 1985 Oct 30;146(2):272-81. doi: 10.1016/0042-6822(85)90010-8.
Early events in the infection of the human T-lymphotropic virus type-I (HTLV-I)-positive MT-4 cell line by the acquired immune deficiency syndrome (AIDS) retrovirus HTLV-III were investigated. The virus was adsorbed completely to the cells within 60 min incubation after inoculation of the virus. Then, infected MT-4 cells started to produce the HTLV-III-specific antigens between 12 and 24 hr postinfection. Synthesis of the viral antigens consisting of 120K, 46K, 24K, and 17K polypeptides was suppressed by the treatment of the virus-infected MT-4 cells with cytosine arabinoside (Ara-C) or by the treatment of the virus with anti-HTLV-III-positive sera. The progeny of the virus released from the infected MT-4 cells was titrated by a newly developed plaque-forming assay method and reverse transcriptase activity. The maximum activity of HTLV-III (3 X 10(5) PFU/ml) was observed on Days 4 and 5 p.i. Most of the viral activities in this preparation were ascribed to HTLV-III, and not to HTLV-I. No phenotypic mixing between HTLV-III and HTLV-I was discerned, although MT-4 cells were HTLV-I-producer cell line. Thus, HTLV-III-infected MT-4 cells are thought to be useful in further study of the interaction between host cells and the virus, and appear to be a good viral source for the analysis of the virus.
对获得性免疫缺陷综合征(AIDS)逆转录病毒HTLV-III感染人I型嗜T淋巴细胞病毒(HTLV-I)阳性MT-4细胞系的早期事件进行了研究。接种病毒后,在60分钟的孵育时间内,病毒完全吸附到细胞上。然后,受感染的MT-4细胞在感染后12至24小时开始产生HTLV-III特异性抗原。用阿糖胞苷(Ara-C)处理病毒感染的MT-4细胞或用抗HTLV-III阳性血清处理病毒,可抑制由120K、46K、24K和17K多肽组成的病毒抗原的合成。通过新开发的噬斑形成测定方法和逆转录酶活性对从受感染的MT-4细胞释放的病毒子代进行滴定。在感染后第4天和第5天观察到HTLV-III的最大活性(3×10⁵ PFU/ml)。该制剂中的大多数病毒活性归因于HTLV-III,而非HTLV-I。尽管MT-4细胞是HTLV-I产生细胞系,但未发现HTLV-III与HTLV-I之间有表型混合。因此,HTLV-III感染的MT-4细胞被认为在进一步研究宿主细胞与病毒之间的相互作用方面是有用的,并且似乎是用于病毒分析的良好病毒来源。