Cavalieri S J, Snyder I S
Infect Immun. 1982 May;36(2):455-61. doi: 10.1128/iai.36.2.455-461.1982.
To gain further evidence that Escherichia coli alpha-hemolysin has a role in pathogenesis, its effect on human peripheral leukocyte viability was studied in vitro. Viability of leukocytes exposed to low doses of alpha-hemolysin decreased nearly 10-fold within 15 min of exposure. This response was dose and time dependent and was neutralized by antiserum, heat, proteases, and lipase. To gain further evidence that alpha-hemolysin was the molecule responsible for leukotoxicity, preparations of alpha-hemolysin were passed through a hydrophobic interaction chromatographic column. Alpha-hemolysin prepared in this way retained its leukotoxic activity. Both hemolytic and leukotoxic activities copurified at the same ratio and were inactivated to the same degree by heating at 56 degrees C. Lysis of leukocytes, if it occurs in vivo, would enhance the chances of survival for an invading hemolytic E. coli.
为了进一步证明大肠杆菌α-溶血素在发病机制中起作用,我们在体外研究了它对人外周血白细胞活力的影响。暴露于低剂量α-溶血素的白细胞活力在暴露后15分钟内下降了近10倍。这种反应呈剂量和时间依赖性,并可被抗血清、加热、蛋白酶和脂肪酶中和。为了进一步证明α-溶血素是导致白细胞毒性的分子,将α-溶血素制剂通过疏水相互作用色谱柱。以这种方式制备的α-溶血素保留了其白细胞毒性活性。溶血活性和白细胞毒性活性以相同比例共纯化,并在56℃加热时被同等程度地灭活。如果白细胞裂解发生在体内,将增加侵袭性溶血大肠杆菌的存活机会。