Stoye J P, Moroni C
J Gen Virol. 1984 Feb;65 ( Pt 2):317-26. doi: 10.1099/0022-1317-65-2-317.
In addition to the known induction of xenotropic endogenous virus in B-mitogen-stimulated murine lymphocyte cultures, distinguishable defective viruses were also induced in different mouse strains (NFS/N, 129, BALB/c). AKR cells produced xenotropic virus and also, in contrast to BALB/c, ecotropic virus. The drug bromodeoxyuridine appeared to have differential effects on virus expression, amplifying xenotropic virus induction but inhibiting the spontaneous production of the ecotropic virus in AKR cultures and of the defective virus in NFS/N cells. Infecting stimulated BALB/c or AKR cultures with Friend leukaemia virus resulted in the production of ecotropic-xenotropic pseudotype viruses, indicating that the infecting ecotropic virus replicates in the cells in which xenotropic virus is induced. No pseudotypes or recombinants were observed following infection of spleen cells releasing defective viruses. Friend leukaemia virus and xenotropic virus with an ecotropic envelope replicated equally well in stimulated lymphocytes from the different strains examined. Taken together, these findings indicate that the non-infectious viruses are encoded by defective proviruses, rather than resulting from faulty, host cell-controlled, virus maturation.
除了在B细胞有丝分裂原刺激的小鼠淋巴细胞培养物中已知可诱导嗜异性内源性病毒外,在不同小鼠品系(NFS/N、129、BALB/c)中还诱导出了可区分的缺陷病毒。AKR细胞产生嗜异性病毒,而且与BALB/c不同的是,还产生亲嗜性病毒。药物溴脱氧尿苷似乎对病毒表达有不同影响,增强嗜异性病毒的诱导,但抑制AKR培养物中亲嗜性病毒的自发产生以及NFS/N细胞中缺陷病毒的自发产生。用弗氏白血病病毒感染受刺激的BALB/c或AKR培养物会导致产生亲嗜性-嗜异性假型病毒,这表明感染的亲嗜性病毒在诱导嗜异性病毒的细胞中复制。在释放缺陷病毒的脾细胞感染后未观察到假型或重组体。带有亲嗜性包膜的弗氏白血病病毒和嗜异性病毒在检测的不同品系的受刺激淋巴细胞中复制情况相同。综上所述,这些发现表明非感染性病毒由缺陷前病毒编码,而不是由有缺陷的、宿主细胞控制的病毒成熟产生。