Svoboda J, Geryk J, Karakoz I, Rejthar A
Folia Biol (Praha). 1985;31(2):135-51.
Sarcomas appeared after long latency with a frequency of about 2% in Brown Leghorn and (CB X IC)F1 chickens after intraembryonic and neonatal inoculation of transformation-defective mutants of ASVs subgroup C. Only the freshly isolated td mutants, td daPR-C and td daPR-C morphf, exhibited the tumorigenic activity, whereas the standard td mutants induced no sarcomas. Two (862 and 2257) out of four tumours could be transplanted in young chickens and produced low titres of transforming virus. The other two tumours were not transplantable and devoid of any transforming virus. Viruses 862 and 2257 are clearly defective in replication, virus 2257 cannot be complemented efficiently by any helper virus in vitro. The low titre of virus 2257 is not caused by interference with a helper virus of the same subgroup specificity. Both viruses are highly tumorigenic in vivo.
在鸡胚内和新生期接种ASV C亚群转化缺陷型突变体后,经过较长潜伏期,棕色来航鸡和(CB×IC)F1鸡中出现肉瘤的频率约为2%。只有新鲜分离的td突变体td daPR-C和td daPR-C morphf表现出致瘤活性,而标准td突变体未诱发肉瘤。四只肿瘤中有两只(862和2257)可移植到幼鸡体内,并产生低滴度的转化病毒。另外两只肿瘤不可移植且不含任何转化病毒。病毒862和2257在复制方面明显存在缺陷,病毒2257在体外不能被任何辅助病毒有效互补。病毒2257的低滴度不是由与相同亚群特异性的辅助病毒的干扰引起的。两种病毒在体内均具有高度致瘤性。