König B, König W, Scheffer J, Hacker J, Goebel W
Infect Immun. 1986 Dec;54(3):886-92. doi: 10.1128/iai.54.3.886-892.1986.
We investigated the role of bacterial mannose-resistant fimbriation of S fimbriae (Fim), mannose-resistant hemagglutination (S-Mrh), and hemolysin (Hly) production by an Escherichia coli parent and genetically cloned strains as regards their effect on histamine release from rat mast cells and generation of the chemiluminescence response, leukotriene, and enzyme release from human polymorphonuclear granulocytes. These mediators are involved in the induction of inflammatory disease processes and lead, e.g., to the enhancement of vascular permeability, chemotaxis, aggregation of granulocytes (leukotriene B4), lysosomal enzyme release, and smooth-muscle contraction (leukotrienes C4, D4, and E4). The content of azurophilic and specific granules in polymorphonuclear granulocytes consists of highly reactive enzymes which amplify inflammatory reactions. Washed bacteria (E. coli 764 Hly+/-, E. coli 21085 Hly+/- Fim+/- Mrh+/-), as well as their culture supernatants, were analyzed at various times during their growth cycle. No differences exist between parent and cloned or mutant strains with respect to their outer membrane proteins and lipopolysaccharide pattern. Washed bacteria [E. coli 764 and 21085(pANN202-312)] which produced hemolysin, unlike Hly- strains, induced high levels of histamine release from rat mast cells and led to a significant chemiluminescence response and enzyme and leukotriene release from human polymorphonuclear granulocytes. Bacterial culture supernatants from Hly+ and secreting strains showed similar results with the exception of E. coli 21085(pANN202-312), which is a hemolysin-producing but not a secretory strain. Our data suggest a potent role for hemolysin as a stimulus for noncytotoxic mediator release from various cells. Furthermore, we showed that the presence of Fim and S Mrh potentiates mediator release. The simultaneous presence of Mrh and Fim [E. coli 535/21(pANN801-4)] increased mediator release compared with Mrh+ Fim- strains [E. coli 536/21(pANN801-1)]. E. coli 536/21 (Msh- Mrh- Fim- Hly-) did not induce mediator release.
我们研究了大肠杆菌亲本及其基因克隆菌株的菌毛(Fim)、甘露糖抗性血凝素(S-Mrh)以及溶血素(Hly)的产生对大鼠肥大细胞组胺释放、人多形核粒细胞化学发光反应、白三烯生成及酶释放的影响。这些介质参与炎症疾病过程的诱导,例如会导致血管通透性增强、趋化性、粒细胞聚集(白三烯B4)、溶酶体酶释放以及平滑肌收缩(白三烯C4、D4和E4)。多形核粒细胞中的嗜天青颗粒和特异性颗粒的内容物由能放大炎症反应的高活性酶组成。在生长周期的不同时间点对洗涤过的细菌(大肠杆菌764 Hly+/-、大肠杆菌21085 Hly+/- Fim+/- Mrh+/-)及其培养上清液进行了分析。亲本菌株与克隆菌株或突变菌株在外膜蛋白和脂多糖模式方面没有差异。与不产生溶血素的菌株不同,产生溶血素的洗涤过的细菌[大肠杆菌764和21085(pANN202 - 312)]可诱导大鼠肥大细胞释放高水平的组胺,并导致人多形核粒细胞产生显著的化学发光反应以及酶和白三烯释放。来自产生溶血素和分泌型菌株的细菌培养上清液显示出类似的结果,但大肠杆菌21085(pANN202 - 312)除外,它是一个产生溶血素但不分泌的菌株。我们的数据表明溶血素作为一种刺激物,在从各种细胞释放非细胞毒性介质方面发挥着重要作用。此外,我们表明Fim和S Mrh的存在会增强介质释放。与Mrh+ Fim-菌株[大肠杆菌536/21(pANN801 - 1)]相比,Mrh和Fim同时存在[大肠杆菌535/21(pANN801 - 4)]会增加介质释放。大肠杆菌536/21(Msh- Mrh- Fim- Hly-)不诱导介质释放。