Zhao Kong-Nan, Frazer Ian H
Centre for Immunology and Cancer Research, The University of Queensland, Princess Alexandra Hospital, Brisbane, Queensland 4102, Australia.
J Virol. 2002 Apr;76(7):3359-64. doi: 10.1128/jvi.76.7.3359-3364.2002.
Saccharomyces cerevisiae protoplasts exposed to bovine papillomavirus type 1 (BPV-1) virions demonstrated uptake of virions on electron microscopy. S. cerevisiae cells looked larger after exposure to BPV-1 virions, and cell wall regeneration was delayed. Southern blot hybridization of Hirt DNA from cells exposed to BPV-1 virions demonstrated BPV-1 DNA, which could be detected over 80 days of culture and at least 13 rounds of division. Two-dimensional gel analysis of Hirt DNA showed replicative intermediates, confirming that the BPV-1 genome was replicating within S. cerevisiae. Nicked circle, linear, and supercoiled BPV-1 DNA species were observed in Hirt DNA preparations from S. cerevisiae cells infected for over 50 days, and restriction digestion showed fragments hybridizing to BPV-1 in accord with the predicted restriction map for circular BPV-1 episomes. These data suggest that BPV-1 can infect S. cerevisiae and that BPV-1 episomes can replicate in the infected S. cerevisiae cells.
暴露于1型牛乳头瘤病毒(BPV-1)病毒粒子的酿酒酵母原生质体在电子显微镜下显示出病毒粒子的摄取。暴露于BPV-1病毒粒子后,酿酒酵母细胞看起来更大,细胞壁再生延迟。对暴露于BPV-1病毒粒子的细胞的Hirt DNA进行Southern印迹杂交,显示出BPV-1 DNA,在培养80多天和至少13轮分裂过程中都能检测到。对Hirt DNA的二维凝胶分析显示有复制中间体,证实BPV-1基因组在酿酒酵母内复制。在感染超过50天的酿酒酵母细胞的Hirt DNA制备物中观察到切口环状、线性和超螺旋的BPV-1 DNA种类,限制性消化显示片段与BPV-1杂交,与环状BPV-1附加体的预测限制性图谱一致。这些数据表明BPV-1可以感染酿酒酵母,并且BPV-1附加体可以在受感染的酿酒酵母细胞中复制。