Brand O M, Allen W P
Appl Microbiol. 1970 Sep;20(3):298-302. doi: 10.1128/am.20.3.298-302.1970.
Noninfectious arbovirus antigens were prepared from borate-saline suspensions of infected suckling mouse brain buffered with tris(hydroxmethyl)aminomethane and treated with beta-propiolactone (BPL). The activity and stability of these antigens were enhanced by altering the buffering system, by passing the virus seed through a series of four or more continuous passages in the brains of suckling mice, or by a combination of these procedures. The titers of group A and B arbovirus antigens were comparable to titers of antigens extracted by the conventional sucroseacetone-BPL (SA-BPL) method. Antigens prepared from some ungrouped and Bunyamwera arboviruses by either the borate-saline-BPL or SA-BPL method produced inconsistent results and will require the development of more unique procedures to obtain suitable hemagglutinating antigens.
非感染性虫媒病毒抗原是从用三(羟甲基)氨基甲烷缓冲的感染乳鼠脑硼酸盐 - 盐水悬浮液中制备的,并用β - 丙内酯(BPL)处理。通过改变缓冲系统、使病毒种子在乳鼠脑中连续传代四次或更多次,或通过这些方法的组合,可以提高这些抗原的活性和稳定性。A组和B组虫媒病毒抗原的效价与通过传统蔗糖 - 丙酮 - BPL(SA - BPL)方法提取的抗原效价相当。通过硼酸盐 - 盐水 - BPL或SA - BPL方法从一些未分类的和布尼亚姆韦拉虫媒病毒制备的抗原产生了不一致的结果,需要开发更独特的方法来获得合适的血凝抗原。