Yohn D S, Haendiges V A, Grace J T
J Bacteriol. 1966 May;91(5):1977-85. doi: 10.1128/jb.91.5.1977-1985.1966.
Yohn, David S. (Roswell Park Memorial Institute, Buffalo, N.Y.), Victoria A. Haendiges, and James T. Grace, Jr. Yaba tumor poxvirus synthesis in vitro. I. Cytopathological, histochemical, and immunofluorescent studies. J. Bacteriol. 91:1977-1985. 1966.-Yaba tumor poxvirus synthesis in BSC-1 cell culture was followed sequentially with light microscopy, immunofluorescent microscopy, and various histochemical stains. The first evidence of infection was detected at 24 hr when nucleoli became hypertrophic, reflecting enhanced ribonucleic acid (RNA) synthesis. At 36 hr, deoxyribonucleic acid synthesis was detected in the cytoplasm. This was immediately followed by or associated with antigen synthesis at paranuclear sites and enhanced RNA synthesis in the cytoplasm. Cytoplasmic inclusions were readily apparent at 4 days in initially infected cells. Contiguous spread of virus was judged to have occurred around the third day of infection. The time required to complete the synthetic cycle from time of infection to production of infectious progeny was estimated to be of the order of 60 hr. This cycle is 6 to 10 times longer than for vaccinia virus. By light microscopy, cytopathic effects (CPE) were detectable in 5 days in heavily infected cultures. With 100 units or less of infectious virus, CPE was not readily detected until the 10th to 14th day. At this time, focal areas of infection classified either as microtumors or microplaques were present. Secondary foci appeared during the 4th week of incubation.
约恩,大卫·S.(纽约州布法罗市罗斯韦尔公园纪念研究所),维多利亚·A. 亨迪格斯,以及小詹姆斯·T. 格雷斯。体外雅巴肿瘤痘病毒的合成。I. 细胞病理学、组织化学和免疫荧光研究。《细菌学杂志》91:1977 - 1985。1966年。——通过光学显微镜、免疫荧光显微镜和各种组织化学染色,对雅巴肿瘤痘病毒在BSC - 1细胞培养中的合成过程进行了连续观察。感染的首个迹象在24小时时被检测到,此时核仁肥大,这反映出核糖核酸(RNA)合成增强。36小时时,在细胞质中检测到脱氧核糖核酸合成。紧接着,在核旁位点出现抗原合成,并伴有细胞质中RNA合成增强。最初感染的细胞在4天时细胞质内包含体清晰可见。判断病毒在感染后第三天左右发生了连续传播。从感染到产生有感染性后代完成合成周期所需的时间估计约为60小时。这个周期比痘苗病毒的周期长6至10倍。通过光学显微镜观察,在感染严重的培养物中,5天时可检测到细胞病变效应(CPE)。对于100个单位或更少的感染性病毒,直到第10至14天才容易检测到CPE。此时,出现了分类为微肿瘤或微斑块的局部感染区域。在培养的第4周出现了继发性病灶。