N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation.
Glycobiology. 2013 Apr;23(4):475-85. doi: 10.1093/glycob/cws222. Epub 2013 Jan 2.
Shigella flexneri is the major human pathogen causing shigellosis. O-antigens of all S. flexneri serotypes (except for serotype 6) share the →2)-α-l-Rhap(III)-(1 → 2)-α-l-Rhap(II)-(1 → 3)-α-l-Rhap(I)-(1 → 3)-β-d-GlcpNAc-(1→ basic O-unit, whereas differences between the serotypes are conferred by phage-encoded glucosylation and/or O-acetylation at various positions. Recently, in serotype X and 4a variants called Xv and 4av, respectively, O-antigen modification with phosphoethanolamine (PEtN) has been identified, which is encoded by a plasmid-borne gene (lpt-O) for a PEtN-transferase and confers the monoclonal antibody IV-1(MASF IV-1) determinant to the bacteria. In this study, we elucidated the O-antigen structure of serotype Yv, another MASF IV-1-positive novel variant of S. flexneri. The serotype Yv O-antigen has the same basic carbohydrate backbone structure as that of the "classical" serotype Y, but differs in the presence of PEtN at position 3 of Rha(III) (major) or both Rha(II) and Rha(III) (minor). This pattern is similar to that of serotype 4av, but different from the pattern of serotype Xv, which is characterized by major PEtN modification on Rha(II). In serotype Yv, mono- and bisphosphorylated O-units generate a block-copolymeric structure, the former being partially O-acetylated at position 6 of GlcNAc and the latter lacking O-acetylation. Functional analysis revealed a correlation between the serotype-specific PEtN modification pattern and the lpt-O variation in different serotypes: lpt-O(RII) in serotype Xv is better tuned for phosphorylation of Rha(II) and lpt-O(RIII) in serotypes Yv and 4av for phosphorylation of Rha(III). These data enhance our knowledge of S. flexneri serotype conversion mechanisms and help to understand the biosynthesis process of the new O-antigen variants.
福氏志贺菌是引起志贺菌病的主要人类病原体。所有福氏志贺菌血清型(血清型 6 除外)的 O-抗原都共享→2)-α-l-Rhap(III)-(1 → 2)-α-l-Rhap(II)-(1 → 3)-α-l-Rhap(I)-(1 → 3)-β-d-GlcpNAc-(1→基本 O-单元,而血清型之间的差异则由噬菌体编码的葡萄糖基化和/或在不同位置的 O-乙酰化赋予。最近,在分别称为 Xv 和 4av 的血清型 X 和 4a 变体中,已经鉴定出 O-抗原的磷酸乙醇胺(PEtN)修饰,该修饰由质粒携带的 PEtN 转移酶基因(lpt-O)编码,并赋予细菌单克隆抗体 IV-1(MASF IV-1)决定簇。在这项研究中,我们阐明了另一种 MASF IV-1 阳性的福氏志贺菌新型变体血清型 Yv 的 O-抗原结构。血清型 Yv 的 O-抗原具有与“经典”血清型 Y 相同的基本碳水化合物骨架结构,但在 Rha(III)(主要)或 Rha(II)和 Rha(III)(次要)的 3 位存在 PEtN 。这种模式类似于血清型 4av,但与血清型 Xv 不同,血清型 Xv 的特征是 Rha(II)上主要的 PEtN 修饰。在血清型 Yv 中,单磷酸化和双磷酸化的 O-单元产生嵌段共聚物结构,前者在 GlcNAc 的 6 位部分乙酰化,后者则缺乏 O-乙酰化。功能分析表明,不同血清型中特定于血清型的 PEtN 修饰模式与 lpt-O 变化之间存在相关性:血清型 Xv 中的 lpt-O(RII) 更适合于 Rha(II)的磷酸化,而血清型 Yv 和 4av 中的 lpt-O(RIII) 更适合于 Rha(III)的磷酸化。这些数据增强了我们对福氏志贺菌血清型转换机制的认识,并有助于理解新 O-抗原变体的生物合成过程。