Calisher C H, Maness K S
Appl Microbiol. 1970 Sep;20(3):398-404. doi: 10.1128/am.20.3.398-404.1970.
Mice were inoculated with St. Louis encephalitis (SLE), Flanders (FLAN), California (CE), or Tensaw (TEN) viruses. At fixed intervals after inoculation, brains from these mice were collected and assayed for infective virus and complement-fixing, hemagglutinating, and precipitating antigens. Detectability of these antigens was correlated with the appearance of signs of illness in the mice. Infective virus appeared 64, 48, 48, and 40 hr before signs of illness and 90, 86, 64, and 56 hr before death in mice inoculated with SLE, FLAN, CE, and TEN viruses, respectively. Diagnostic antigens were also detected well before signs of illness appeared. These findings were applied to the isolation of viruses from field-collected specimens. It was shown that by harvesting tissues at appropriate intervals these viruses could be detected and identified more rapidly than by conventional techniques with mice.
给小鼠接种圣路易斯脑炎(SLE)、佛兰德斯(FLAN)、加利福尼亚(CE)或滕索(TEN)病毒。接种后每隔固定时间,收集这些小鼠的大脑,检测其中的感染性病毒以及补体结合、血凝和沉淀抗原。这些抗原的可检测性与小鼠发病体征的出现相关。在接种SLE、FLAN、CE和TEN病毒的小鼠中,感染性病毒分别在发病体征出现前64、48、48和40小时以及死亡前90、86、64和56小时出现。诊断性抗原也在发病体征出现之前很久就能被检测到。这些发现被应用于从野外采集的标本中分离病毒。结果表明,通过在适当的时间间隔采集组织,这些病毒比用传统的小鼠技术能更快地被检测和鉴定出来。