Levitt N H, Miller H V, Pedersen C E, Eddy G A
Am J Trop Med Hyg. 1975 Jan;24(1):127-30. doi: 10.4269/ajtmh.1975.24.127.
The development of a new diagnostic procedure for the identification of Venezvelan, eastern and western equine encephalomyelitis (VEE, EEE, WEE) viruses is described. The procedure utilizes virus precipitation with reference fluorescein-conjugated gamma globulin, followed by cellulose acetate electrophoresis. Clinical specimens containing varying concentrations of virus yielded, in primary duck embryo cell culture, sufficient virus for detection within 22 to 44 hours. Identification of VEE, EEE and WEE virus in specimens was accomplished by microprecipitation within this time. In contrast to conventional identification methods, our procedure eliminates the cost of utilizing laboratory animals and considerably reduces the time required for virus identification.
本文描述了一种用于鉴定委内瑞拉马脑炎病毒、东部马脑炎病毒和西部马脑炎病毒(VEE、EEE、WEE)的新诊断方法的开发。该方法利用参考荧光素标记的γ球蛋白进行病毒沉淀,随后进行醋酸纤维素电泳。在原代鸭胚细胞培养中,含有不同浓度病毒的临床标本在22至44小时内产生了足够用于检测的病毒。在此时间内,通过微量沉淀法完成了标本中VEE、EEE和WEE病毒的鉴定。与传统鉴定方法相比,我们的方法消除了使用实验动物的成本,并大大缩短了病毒鉴定所需的时间。