Altaner C, Bán J, Altanerová V, Burny A, Kettmann R
Cancer Research Institute, Slovak Academy of Sciences, Bratislava, Czechoslovakia.
Neoplasma. 1987;34(6):641-52.
Several single-cell clones were isolated from a fetal lamb kidney cell line (FLK) persistently infected with bovine leukemia virus (BLV). The majority of isolated cell clones were virus productive, several were nonproductive based on the determination of the activity of reverse transcriptase and production of 3H-uridine labeled virus particles. Two nonproductive clones, NP-1 and NP-2, were further characterized in comparison with the virus productive cells. All clones contained three integrated BLV proviruses in the nonproducer cells. The virus specific mRNAs were expressed both in the virus productive and nonproductive cells. The virus-specific protein products were found different in the nonproducing cells. The gag pol precursor Pr145 was missing in NP-1 cells, in NP-2 its Mr was 120 only. In NP-2 cells the precursors Pr70gag and Pr45gag were absent. The env precursor gPr72 and both of the two glycoproteins were detected. The nonproductive cells NP-2 produced mainly env gene products, therefore they were tested as a potential material for anti-BLV vaccine. The NP-2 cells after inoculation to rats and cattle were able to induce formation of neutralizing antibodies directed against the env gene products.
从持续感染牛白血病病毒(BLV)的胎羊肾细胞系(FLK)中分离出几个单细胞克隆。根据逆转录酶活性测定和3H-尿苷标记病毒颗粒的产生情况,大多数分离出的细胞克隆具有病毒生产能力,有几个则无此能力。与具有病毒生产能力的细胞相比,对两个无生产能力的克隆NP-1和NP-2进行了进一步鉴定。所有克隆在无生产能力的细胞中都含有三个整合的BLV前病毒。病毒特异性mRNA在具有病毒生产能力和无生产能力的细胞中均有表达。在无生产能力的细胞中发现病毒特异性蛋白质产物有所不同。NP-1细胞中缺少gag pol前体Pr145,在NP-2中其分子量仅为120。在NP-2细胞中,前体Pr70gag和Pr45gag缺失。检测到env前体gPr72和两种糖蛋白。无生产能力的细胞NP-2主要产生env基因产物,因此将它们作为抗BLV疫苗的潜在材料进行了测试。将NP-2细胞接种到大鼠和牛体内后,能够诱导产生针对env基因产物的中和抗体。