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首页> 外文期刊>The Journal of biological chemistry >Structural Characterization of Streptococcus pneumoniae Serotype 9A Capsule Polysaccharide Reveals Role of Glycosyl 6-O-Acetyltransferase wcjE in Serotype 9V Capsule Biosynthesis and Immunogenicity
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Structural Characterization of Streptococcus pneumoniae Serotype 9A Capsule Polysaccharide Reveals Role of Glycosyl 6-O-Acetyltransferase wcjE in Serotype 9V Capsule Biosynthesis and Immunogenicity

机译:链球菌血管型9A胶囊多糖的结构表征揭示了糖基6-O-乙酰转移酶WCJE在血清型9V胶囊生物合成和免疫原性中的作用

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摘要

The putative capsule O-acetyltransferase gene wcjE is highly conserved across various Streptococcus pneumoniae serotypes, but the role of the gene in capsule biosynthesis and bacterial fitness remains largely unclear. Isolates expressing pneumococcal serotype 9A arise from precursors expressing wcjE-associated serotype 9V through loss-of-function mutation to wcjE. To define the biosynthetic role of 9V wcjE, we characterized the structure and serological properties of serotype 9V and 9A capsule polysaccharide (PS). NMR data revealed that both 9V and 9A PS are composed of an identical pentasaccharide repeat unit, as reported previously. However, in sharp contrast to previous studies on 9A PS being devoid of any O-acetylation, we identified O-acetylation of α-glucuronic acid and α-glucose in 9A PS. In addition, 9V PS also contained –CH2 O-acetylation of β-N-acetylmannosamine, a modification that disappeared following in vitro recombinatorial deletion of wcjE. We also show that serotyping sera and monoclonal antibodies specific for 9V and 9A bound capsule PS in an O-acetate-dependent manner. Furthermore, IgG and to a lesser extent IgM from human donors immunized with serotype 9V PS displayed stronger binding to 9V compared with 9A PS. We conclude that serotype 9V wcjE mediates 6-O-acetylation of β-N-acetylmannosamine. This PS modification can be selectively targeted by antibodies in immunized individuals, identifying a potential selective advantage for wcjE inactivation and serotype 9A emergence.
机译:推定的胶囊O-乙酰转移酶基因WCJE在各种链球菌血管型血清型中受到高度保守,但基因在胶囊生物合成中的作用仍然很大程度上不清楚。表达肺炎球菌血清型9A的分离物通过与WCJE的功能突变突变表达WCJE相关血清型9V的前体。为了定义9V WCJE的生物合成作用,其特征在于血清型9V和9A胶囊多糖(PS)的结构和血清学特性。 NMR数据显示,如前所述,9V和9A PS均由相同的戊二糖重复单元组成。然而,与先前的9A PS的研究鲜明对比,我们鉴定了任何O-乙酰化,我们鉴定了α-葡萄糖醛酸和α-葡萄糖的α-葡萄糖在9A PS中。此外,9V PS还含有-CH 2 O-乙酰甲烷胺的α-乙酰化,在体外重组缺失后消失的改性WCJE。我们还表明,血清型血清和单克隆抗体特异于9V和9A的胶囊PS,以乙酸依赖性方式。此外,IgG和用血清型9V PS免疫的人供体的较小程度的IgM显示与9a Ps相比显示得更强的结合。我们得出结论,血清型9V WCJE介导β-N-乙酰诺纳胺的6-O-乙酰化。该PS改性可以通过免疫个体中的抗体选择性地靶向,鉴定WCJE灭活和血清型9A的潜在选择性优势。

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