Scaletsky I C, Milani S R, Trabulsi L R, Travassos L R
Departamento de Microbiologia, Imunologia e Parasitologia, Escola Paulista de Medicina, São Paulo, Brazil.
Infect Immun. 1988 Nov;56(11):2979-83. doi: 10.1128/iai.56.11.2979-2983.1988.
The binding factor of enteropathogenic Escherichia coli O111:H- responsible for localized adherence (LA) on HeLa cells was investigated. Inhibition of LA by carbohydrates and lectins showed that the reactive epitope on HeLa cells contains N-acetylgalactosamine units. Treatment of bacteria with EDTA for extraction of lipopolysaccharides eliminated these polymers as binding factors. Such treatment also caused a marked increase in adhesion suggesting steric hindrance by lipopolysaccharides of the LA factor binding capacity. Immunoblotting with rabbit antibodies showed a strong reaction with two components with approximate molecular sizes of 29 and 32 kilodaltons (kDa) present in the outer membrane preparations of bacteria. Both the absorbed rabbit immune serum and the outer membrane preparation of the bacteria inhibited bacterial adhesion by 100%. Outer membrane components were isolated from an N-acetylgalactosamine-agarose column by elution with KSCN, labeled with 125I, and immunoprecipitated with absorbed rabbit hyperimmune antiserum. The only component precipitated was the protein doublet at 29 to 32 kDa corresponding to the components detected by immunoblotting. The predominant component was always the 32-kDa polypeptide. We conclude that this component of the outer membrane is the best candidate for the LA factor in enteropathogenic E. coli.
对引起肠致病性大肠杆菌O111:H - 在HeLa细胞上局部黏附(LA)的黏附因子进行了研究。碳水化合物和凝集素对LA的抑制作用表明,HeLa细胞上的反应表位含有N - 乙酰半乳糖胺单元。用EDTA处理细菌以提取脂多糖,消除了这些聚合物作为黏附因子的作用。这种处理还导致黏附显著增加,表明脂多糖对LA因子结合能力存在空间位阻。用兔抗体进行免疫印迹显示,与细菌外膜制剂中存在的两种分子大小约为29和32千道尔顿(kDa)的成分发生强烈反应。吸收的兔免疫血清和细菌的外膜制剂均能100%抑制细菌黏附。通过用KSCN洗脱从N - 乙酰半乳糖胺 - 琼脂糖柱上分离出外膜成分,用125I标记,并用吸收的兔超免疫抗血清进行免疫沉淀。唯一沉淀的成分是29至32 kDa的蛋白质双峰,与免疫印迹检测到的成分相对应。主要成分始终是32 kDa的多肽。我们得出结论,外膜的这一成分是肠致病性大肠杆菌中LA因子的最佳候选者。