Hoien-Dalen P S, Rosenbusch R F, Roth J A
Department of Veterinary Microbiology and Preventive Medicine, College of Veterinary Medicine, Iowa State University, Ames 50011.
Am J Vet Res. 1990 Feb;51(2):191-6.
The cytotoxic effect of Moraxella bovis 118F on bovine neutrophils was evaluated and characterized by use of a 51Cr release assay. Neutrophils harvested from healthy adult cattle were labeled with 51Cr. The leukocidic activity produced by M bovis 118F, a hemolytic strain of M bovis, was heat-labile. A live culture of strain 118F, at a ratio of 100 bacteria/neutrophil, released 97.7% of the 51Cr from labeled neutrophils. Neither a heat-killed preparation of M bovis 118F nor a live or heat-killed preparation of M bovis IBH63 (a nonhemolytic and nonpathogenic strain) induced significant (P greater than 0.05) release of 51Cr. Moraxella bovis 118F broth culture filtrates prepared for evaluation of leukocidic activity also were evaluated for hemolytic activity. These 2 toxic activities had several characteristics in common. Both were filterable, heat-labile, produced by a hemolytic strain, and were released during early logarithmic phase growth from broth cultures. Leukocidic and hemolytic activities were protected from degradation by phenylmethyl sulfonyl fluoride, a serine protease inhibitor. Leukocidic and hemolytic activities were dependent on calcium ions. Filtrate resulted in 54.1% 51Cr release from labeled neutrophils and contained 646.7 hemolytic U/ml, respectively, when saline (0.85% NaCl) + 10 mM CaCl2 solution was used as diluent. Neither saline solution nor saline + 10 mM MgCl2 solution supported leukocidic or hemolytic activity. Serum, obtained from several calves 10 to 38 days after M bovis inoculation, substantially neutralized leukocidic and hemolytic activities, compared with paired preinoculation serum samples.(ABSTRACT TRUNCATED AT 250 WORDS)
利用铬-51释放试验评估并表征了牛莫拉菌118F对牛中性粒细胞的细胞毒性作用。从健康成年牛采集的中性粒细胞用铬-51进行标记。牛莫拉菌的溶血菌株118F产生的杀白细胞活性是热不稳定的。118F菌株的活培养物以100个细菌/中性粒细胞的比例,使标记的中性粒细胞释放出97.7%的铬-51。牛莫拉菌118F的热灭活制剂以及牛莫拉菌IBH63(非溶血和非致病菌株)的活制剂或热灭活制剂均未诱导铬-51的显著(P大于0.05)释放。为评估杀白细胞活性而制备的牛莫拉菌118F肉汤培养滤液也进行了溶血活性评估。这两种毒性活性有几个共同特征。两者均可滤过、热不稳定,由溶血菌株产生,且在肉汤培养的对数生长期早期释放。杀白细胞和溶血活性可被丝氨酸蛋白酶抑制剂苯甲基磺酰氟保护不被降解。杀白细胞和溶血活性依赖于钙离子。当使用生理盐水(0.85%氯化钠)+10 mM氯化钙溶液作为稀释剂时,滤液分别导致标记的中性粒细胞释放54.1%的铬-51,且含有646.7溶血单位/毫升。生理盐水溶液或生理盐水+10 mM氯化镁溶液均不支持杀白细胞或溶血活性。与配对的接种前血清样本相比,在接种牛莫拉菌后10至38天从几头小牛获得的血清可显著中和杀白细胞和溶血活性。(摘要截短于250字)