犊牛接种19株流产布鲁氏菌血清的色谱研究。

C E Rice, D C Alexander, B B Barrett
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引用次数: 0

摘要

用凝集试验在接种流产布鲁氏菌19株4天后的犊牛血清中检测到抗体的存在。在接种疫苗后7至10天,滴度达到最大值。蔗糖密度梯度超离心显示,最早的抗体是巨球蛋白,IgM (19Sgamma;gammaM)球蛋白。较轻的抗体,IgG (7Sgamma(2));-球蛋白,几天后出现。随着时间的推移,抗体滴度下降,IgM下降的速度略快于IgG。在大约7个月后重新接种疫苗后,IgM和IgG均迅速上升。采用阴离子交换柱层析(deae -纤维素)和凝胶过滤(Sephadex G-200)分离两种形式的抗体。前一种方法采用梯度缓冲系统,效率更高;IgG抗体出现在pH 7.8 ~ 8.0、离子强度低(0.03M)的早期洗脱液中,IgM抗体出现在pH低于6.0、摩尔浓度增加到0.2以上的较晚洗脱液中。早在疫苗接种后5天,DEAE纤维素层析就能检测IgG和IgM血清。
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Chromatographic studies of sera from calves vaccinated with brucella abortus, strain 19.

The presence of antibody was detected by agglutination tests in the serum of calves four days after vaccination with Brucella abortus strain 19. Titres had reached a maximum by seven to ten days post-vaccination. Sucrose density-gradient ultracentrifugation demonstrated that the earliest antibodies were macroglobulins, IgM (19Sgamma; gammaM)-globulins. Lighter antibodies, IgG (7Sgamma(2); gammaG)-globulins, appeared a few days later. With time, antibody titres fell, IgM declining somewhat more quickly than IgG. After revaccination some seven months later, there was a rapid rise in both IgM and IgG.Anion-exchange column chromatography (DEAE-cellulose) and gel filtration (Sephadex G-200) were applied in separating the two forms of antibody. The former method, in which a gradient buffer system was used, proved to be the more efficient; the IgG antibodies apeared in early eluates at pH 7.8 to 8.0 and low ionic strength, 0.03M, whereas IgM was eluted late when the pH had fallen below 6.0 and the molarity had increased to beyond 0.2. DEAE cellulose chromatography detected IgG as well as IgM sera collected as early as five days after vaccination.

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