Urbina Felipe, Nordmark Eva-Lisa, Yang Zhennai, Weintraub Andrej, Scheutz Flemming, Widmalm Göran
Department of Laboratory Medicine, Division of Clinical Bacteriology, Karolinska Institutet, Karolinska University Hospital, Huddinge, S-141 86 Stockholm, Sweden.
Carbohydr Res. 2005 Mar 21;340(4):645-50. doi: 10.1016/j.carres.2005.01.001.
The structure of the O-antigen polysaccharide (PS) from the enteroaggregative Escherichia coli strain 180/C3 has been determined. Sugar and methylation analysis together with (1)H and (13)C NMR spectroscopy were the main methods used. The PS is composed of tetrasaccharide repeating units with the following structure: -->2)beta-D-Quip3NAc-(1-->3)beta-D-RIBf-(1-->4)beta-D-Galp-(1-->3)alpha-D-GalpNAc-(1-->. Analysis of NMR data indicates that the presented sequence of sugar residues also represents the biological repeating unit of the O-chain. The structure is closely related to that of O-antigen polysaccharide from E. coli O5 and partially to that of E. coli O65. The difference between the O-antigen from the 180/C3 strain and that of E. coli O5 is the linkage to the D-Quip3NAc residue, which in the latter strain is 4-O-substituted. The E. coli O65 O-antigen contains as part of its linear pentasaccharide repeating unit a similar structural element, namely -->4)-beta-d-GalpA-(1-->3)-alpha-D-GlcpNAc-(1-->2)-beta-D-Quip3NAc-(1-->, thereby indicating that a common epitope could be present for the two polysaccharides. Monospecific anti-E. coli O5 rabbit serum did not distinguish between the two positional isomeric structures neither in slide agglutination nor in an indirect enzyme immunoassay. The anti-O65 serum did react with both the 180/C3 and O5 LPS showing a partial cross-reactivity.
已确定了肠聚集性大肠杆菌菌株180/C3的O抗原多糖(PS)的结构。糖和甲基化分析以及¹H和¹³C NMR光谱是主要使用的方法。该PS由具有以下结构的四糖重复单元组成:→2)β-D-喹诺酮3NAc-(1→3)β-D-核糖醇-(1→4)β-D-半乳糖-(1→3)α-D-氨基半乳糖-(1→。NMR数据分析表明,所呈现的糖残基序列也代表了O链的生物学重复单元。该结构与大肠杆菌O5的O抗原多糖结构密切相关,部分与大肠杆菌O65的结构相关。180/C3菌株的O抗原与大肠杆菌O5的O抗原之间的差异在于与D-喹诺酮3NAc残基的连接,在后者菌株中该残基是4-O-取代的。大肠杆菌O65的O抗原在其线性五糖重复单元中包含一个类似的结构元件,即→4)-β-D-半乳糖醛酸-(1→3)-α-D-氨基葡萄糖-(1→2)-β-D-喹诺酮3NAc-(1→,从而表明这两种多糖可能存在共同表位。单特异性抗大肠杆菌O5兔血清在玻片凝集试验和间接酶免疫测定中均无法区分这两种位置异构体结构。抗O65血清与180/C3和O5 LPS均发生反应,显示出部分交叉反应性。