Chopra H C, Shibley G P
John L. Smith Memorial for Cancer Research, Chas. Pfizer & Company, Inc., Maywood, New Jersey 07607, USA.
J Natl Cancer Inst. 1967 Aug;39(2):241-55.
Infecting mouse bone marrow cells (JLS-V9) with cell-free Rauscher leukemia virus demonstrated that monolayers of JLS-V9 cells were susceptible to infection with both cell-free plasma and tissue-culture-propagated Rauscher virus. The infected cultures maintained the continuous release of the virus. Cells and concentrated supernatant fluids from infected cells were periodically examined under the electron microscope by thin sectioning and negative staining techniques after inoculation with either mouse plasma or tissue-culture-propagated virus. After adsorption the virus underwent a prolonged eclipse or latent period. Virus budding was initially detected about 10 days after primary infection. These observations were further confirmed by the simultaneous appearance of extracellular virus. The budding process was followed by accelerated virus multiplication which reached maximum production 2-3 weeks later. Before the onset of budding no significant morphologic changes were seen in the infected cells.
用无细胞的劳氏肉瘤病毒感染小鼠骨髓细胞(JLS-V9)表明,JLS-V9细胞单层对无细胞血浆和组织培养增殖的劳氏病毒均易感染。受感染的培养物持续释放病毒。在用小鼠血浆或组织培养增殖的病毒接种后,通过超薄切片和负染色技术,定期在电子显微镜下检查来自受感染细胞的细胞和浓缩的上清液。吸附后,病毒经历了较长时间的隐蔽期或潜伏期。初次感染后约10天最初检测到病毒出芽。细胞外病毒的同时出现进一步证实了这些观察结果。出芽过程之后是病毒增殖加速,2-3周后达到最大产量。在出芽开始之前,在受感染的细胞中未观察到明显的形态学变化。