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Purification of complement-fixing antigens of Rickettsia sennetsu by ether treatment.

机译:通过醚处理纯化立克次体立克次体的补体固定抗原。

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Soluble and particulate complement-fixing antigens of Rickettsia sennetsu were prepared from spleen suspensions of mice infected with the rickettsia and treated with cyclophosphamide. The medium used during purification of antigens, a solution consisting of equal volumes of phosphate-glutamate-sucrose buffer and veronal-buffered saline, was suitable for obtaining antigens with high titers and no anti-complementary activity. By heat treatment, it was demonstrated that the soluble antigen was heat labile and the particulate antigen was heat stable. The soluble antigen was precipitated by 80% saturation with ammonium sulfate. Cross-complement fixation tests using both soluble and particulate antigens revealed that there was no antigenic difference among strains of R. Sennetsu. On the other hand, no cross-activity was observed between R. sennetsu and R. orientalis.
机译:从感染立克次氏体并用环磷酰胺处理的小鼠的脾悬液中制备Sennetsu立克次体的可溶性和颗粒补体固定抗原。抗原纯化过程中使用的培养基,由等体积的磷酸盐-谷氨酸-蔗糖缓冲液和维罗纳缓冲盐水组成的溶液,适用于获得高滴度且无抗互补活性的抗原。通过热处理,证明了可溶性抗原是热不稳定的并且颗粒抗原是热稳定的。用硫酸铵饱和80%沉淀可溶性抗原。使用可溶性和颗粒状抗原的交叉补体固定测试表明,R。Sennetsu菌株之间没有抗原差异。另一方面,在R. sennetsu和R. Orientalis之间没有观察到交叉活性。

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