Svanborg Edén C, Bjursten L M, Hull R, Hull S, Magnusson K E, Moldovano Z, Leffler H
Infect Immun. 1984 Jun;44(3):672-80. doi: 10.1128/iai.44.3.672-680.1984.
The fitness between bacterial adhesins and target cell receptors, determining bacterial adherence to epithelial cells in urinary tract infections, was shown to influence also the interaction with human polymorphonuclear leukocytes (PMNL). Two sets of homogenic strains, constructed to express either, both, or none of the globotetraosylceramide-sensitive (GS) adhesins specific for globoseries glycolipid receptors or the mannose-sensitive (MS) adhesins inhibited by alpha-methyl mannoside were compared regarding charge, hydrophobicity, and binding to PMNL. The mutants of a hydrophilic pyelonephritis strain required MS adhesins for binding to and activation of the PMNL. Removal of the MS adhesins from the mutant carrying both MS and GS adhesins abolished chemiluminescence and binding. A pronounced chemiluminescence reaction was induced by the hydrophobic strain without GS or MS adhesins . Transformants of this strain expressing the MS adhesin bound to and activated the PMNL. Poor binding and activation were found with mutants and transformants carrying only the GS adhesins . The improved reactivity after coating of the PMNL with the appropriate receptor glycolipid supported the previously reported absence of globoseries glycolipids in those cells as the reason for the refractoriness to bacteria with GS adhesins . The mechanism of binding, which improves epithelial cell adhesion, may prevent binding to PMNL, thus improving the survival of Escherichia coli in the kidney.
细菌黏附素与靶细胞受体之间的适配性决定了细菌在尿路感染中对上皮细胞的黏附,研究表明其也会影响细菌与人类多形核白细胞(PMNL)的相互作用。构建了两组同源菌株,分别表达对球系列糖脂受体具有特异性的球四糖基神经酰胺敏感(GS)黏附素、同时表达GS和甘露糖敏感(MS)黏附素(后者可被α-甲基甘露糖苷抑制)或不表达这两种黏附素,比较了这些菌株在电荷、疏水性以及与PMNL结合方面的差异。亲水性肾盂肾炎菌株的突变体需要MS黏附素来结合和激活PMNL。从同时携带MS和GS黏附素的突变体中去除MS黏附素后,化学发光和结合作用消失。没有GS或MS黏附素的疏水性菌株可诱导明显的化学发光反应。表达MS黏附素的该菌株转化体能结合并激活PMNL。仅携带GS黏附素的突变体和转化体的结合及激活能力较差。用适当的受体糖脂包被PMNL后反应性增强,这支持了之前报道的观点,即这些细胞中缺乏球系列糖脂是其对具有GS黏附素的细菌不敏感的原因。改善上皮细胞黏附的结合机制可能会阻止与PMNL的结合,从而提高大肠杆菌在肾脏中的存活率。