首页> 外文期刊>Journal of Clinical Microbiology >Serial propagation of porcine group C rotavirus (pararotavirus) in a continuous cell line and characterization of the passaged virus.
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Serial propagation of porcine group C rotavirus (pararotavirus) in a continuous cell line and characterization of the passaged virus.

机译:猪C轮状病毒(副轮状病毒)在连续细胞系中的连续繁殖和传代病毒的特征。

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The Cowden strain of porcine group C rotavirus (pararotavirus) was adapted to serial passage in a continuous monkey kidney cell line (MA104). Key factors in its successful adaptation included use of virus passaged in primary porcine kidney cells as the initial inoculum, use of roller tubes, and addition of pancreatin to the maintenance medium. A cell culture immunofluorescence test was used to quantitate the virus at each passage level, since a possible cytopathic effect was obscured by the effects of pancreatin. The virus titers dropped after initial passage into MA104 cells but increased thereafter, with peak titers evident after 16 passages (10(7) immunofluorescence U/ml). Immune electron microscopy and genome electropherotyping were used to identify group C rotavirus particles and confirm group C rotavirus double-stranded RNA gel migration patterns, respectively, from infected cell culture supernatants. The electropherotype of the cell culture-propagated group C rotavirus was identical to that of the gut virulent virus from which it was derived. The cell culture-passaged group C rotavirus also retained its infectivity for gnotobiotic pigs. No group A rotavirus was detected in the intestinal contents of the pigs or in cell culture fluids from group C rotavirus-inoculated monolayers with the two former techniques or the cell culture immunofluorescence test. This is the first verified report of serial propagation of a non-group A rotavirus in a continuous cell line.
机译:猪C型轮状病毒(副轮状病毒)的Cowden株适应于在连续猴肾细胞系(MA104)中的连续传代。其成功适应的关键因素包括使用在原代猪肾细胞中传代的病毒作为初始接种物,使用滚管以及在维护培养基中添加胰酶。细胞培养免疫荧光测试用于定量每个传代水平的病毒,因为胰酶的作用掩盖了可能的细胞病变作用。最初进入MA104细胞后,病毒滴度下降,但随后增加,在16次传代后出现明显的峰值滴度(10(7)免疫荧光U / ml)。免疫电子显微镜和基因组电泳法分别从感染的细胞培养上清液中鉴定出C组轮状病毒颗粒并确认C组轮状病毒双链RNA凝胶迁移模式。细胞培养物传播的C组轮状病毒的电泳图谱与衍生自其的肠道强力病毒的电泳图谱相同。经过细胞培养的C型轮状病毒还保留了其对生gnotobiotic猪的感染性。用前两种技术或细胞培养免疫荧光试验,在猪的肠内容物或C组轮状病毒接种的单层细胞培养液中均未检测到A组轮状病毒。这是非A型轮状病毒在连续细胞系中连续繁殖的第一个验证报告。

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