Confer A W, Durham J A
Department of Veterinary Pathology, Oklahoma State University, Stillwater 74078.
Am J Vet Res. 1992 May;53(5):646-52.
Pasteurella haemolytica was grown in nonsupplemented cell culture medium, or in medium supplemented with bovine serum albumin (BSA) for 24 hours. The production of leukotoxin (LKT) and endotoxin was sequentially evaluated, as were bacterial antigens associated with bacterial cell lysates and culture supernates. Supplementation of medium with BSA had no effect on bacterial growth curves; however, LKT activity was detected earlier and was greater in culture supernates from BSA-supplemented media than from nonsupplemented medium. Leukotoxin antigen (105 kDa) was detected in culture supernates, using a monoclonal antibody, immunoblot analysis, and densitometry. The relative concentrations of LKT antigen were proportional to LKT activity. Endotoxin activity was initially lowest in the culture supernates from nonsupplemented medium, but increased during the incubation period, whereas endotoxin activity in BSA-supplemented culture supernates decreased with time in culture. In culture supernates from nonsupplemented medium, the number of antigenic bands identified by immunoblot analysis with hyperimmune anti-P haemolytica and densitometry was greater than in culture supernates from supplemented media. In bacterial lysates, a 95-kDa antigen was the major antigen detected, using the anti-LKT monoclonal antibody. The concentration of that antigen varied among lysates from nonsupplemented medium and BSA-supplemented media. Using hyperimmune anti-P haemolytica serum, minor differences were seen in the relative quantities of lysate-associated antigens dependent on time in culture and medium used. Among the major antigens seen, differences were most apparent for 150-, 100-, and 87-kDa antigens, whereas differences were not obvious for 42- 40-, and 30-kDa antigens.(ABSTRACT TRUNCATED AT 250 WORDS)
溶血巴斯德菌在未添加成分的细胞培养基中培养,或在添加牛血清白蛋白(BSA)的培养基中培养24小时。依次评估白细胞毒素(LKT)和内毒素的产生情况,以及与细菌细胞裂解物和培养上清液相关的细菌抗原。向培养基中添加BSA对细菌生长曲线没有影响;然而,在添加BSA的培养基的培养上清液中,LKT活性更早被检测到且更高,高于未添加培养基的培养上清液。使用单克隆抗体、免疫印迹分析和光密度测定法在培养上清液中检测到白细胞毒素抗原(105 kDa)。LKT抗原的相对浓度与LKT活性成正比。未添加培养基的培养上清液中内毒素活性最初最低,但在培养期间增加,而添加BSA的培养上清液中的内毒素活性随培养时间下降。在未添加培养基的培养上清液中,用超免疫抗溶血巴斯德菌血清进行免疫印迹分析和光密度测定法鉴定出的抗原条带数量多于添加培养基的培养上清液。在细菌裂解物中,使用抗LKT单克隆抗体检测到的主要抗原是一种95 kDa的抗原。该抗原的浓度在未添加培养基和添加BSA的培养基的裂解物中有所不同。使用超免疫抗溶血巴斯德菌血清,根据培养时间和所用培养基的不同,在裂解物相关抗原的相对量上观察到微小差异。在所观察到的主要抗原中,150 kDa、100 kDa和87 kDa抗原的差异最为明显,而42 kDa、40 kDa和30 kDa抗原的差异不明显。(摘要截断于250字)