Diaz R, Jones L M, Leong D, Wilson J B
J Bacteriol. 1968 Oct;96(4):893-901. doi: 10.1128/jb.96.4.893-901.1968.
Surface antigens of smooth brucellae were extracted by ether-water, phenol-water, trichloroacetic acid, and saline and examined by immunoelectrophoresis and gel diffusion with antisera from infected and immunized rabbits. Ether-water extracts of Brucella melitensis contained a lipopolysaccharide protein component, which was specific for the surface of smooth brucellae and was correlated with the M agglutinogen of Wilson and Miles, a polysaccharide protein component devoid of lipid which was not restricted to the surface of smooth brucellae and was not correlated with the smooth agglutinogen (component 1), and several protein components which were associated with internal antigens of rough and smooth brucellae. Immunoelectrophoretic analysis of ether-water extracts of B. abortus revealed only two components, a lipopolysaccharide protein component, which was correlated with the A agglutinogen, and component 1. Component 1 from B. melitensis and B. abortus showed identity in gel diffusion tests, whereas component M from B. melitensis and component A from B. abortus showed partial identity with unabsorbed antisera and no cross-reactions with monospecific sera. Attempts to prepare monospecific sera directly by immunization of rabbits with cell walls or ether-water extracts were unsuccessful. Absorption of antisera with heavy fraction of ether-water extracts did not always result in monospecific sera. It was concluded (as has been described before) that the A and M antigens are present on a single antigenic complex, in different proportions depending upon the species and biotype, and that this component is a lipopolysaccharide protein complex of high molecular weight that diffuses poorly through agar gel. Components 1, A, and M were also demonstrated in trichloroacetic acid and phenol-water extracts. With all extracts, B. melitensis antigen showed greater diffusibility in agar than B. abortus antigens. After mild acid hydrolysis, B. abortus ether-water extract was able to diffuse more readily.
用乙醚 - 水、苯酚 - 水、三氯乙酸和生理盐水提取光滑型布鲁氏菌的表面抗原,并采用感染和免疫兔的抗血清通过免疫电泳和凝胶扩散法进行检测。羊种布鲁氏菌的乙醚 - 水提取物含有一种脂多糖蛋白成分,它对光滑型布鲁氏菌表面具有特异性,并且与威尔逊和迈尔斯的M凝集原相关;一种不含脂质的多糖蛋白成分,它并不局限于光滑型布鲁氏菌表面,且与光滑凝集原(成分1)无关;还有几种与粗糙型和光滑型布鲁氏菌内部抗原相关的蛋白成分。流产布鲁氏菌乙醚 - 水提取物的免疫电泳分析仅显示出两种成分,一种脂多糖蛋白成分,它与A凝集原相关,以及成分1。羊种布鲁氏菌和流产布鲁氏菌的成分1在凝胶扩散试验中显示相同,而羊种布鲁氏菌的成分M和流产布鲁氏菌的成分A与未吸收的抗血清显示部分相同,且与单特异性血清无交叉反应。试图通过用细胞壁或乙醚 - 水提取物免疫兔直接制备单特异性血清未成功。用乙醚 - 水提取物的重馏分吸收抗血清并不总是能得到单特异性血清。得出的结论是(如之前所描述的),A和M抗原存在于单一抗原复合物上,其比例因菌种和生物型而异,并且该成分是一种高分子量的脂多糖蛋白复合物,在琼脂凝胶中扩散性较差。成分1、A和M也在三氯乙酸和苯酚 - 水提取物中得到证实。对于所有提取物,羊种布鲁氏菌抗原在琼脂中的扩散性比流产布鲁氏菌抗原更强。轻度酸水解后,流产布鲁氏菌乙醚 - 水提取物能够更易扩散。