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从副溶血性弧菌O2和不可分型菌株KX-V212的脂多糖中分离出的5,7-二氨基-3,5,7,9-四脱氧-壬-2-酮糖酸的结构和血清学特征

Structure and serological characterization of 5,7-diamino-3,5,7,9-tetradeoxy-non-2-ulosonic acid isolated from lipopolysaccharides of Vibrio parahaemolyticus O2 and O-untypable strain KX-V212.

作者信息

Hashii Noritaka, Isshiki Yasunori, Iguchi Takehiro, Hisatsune Kazuhito, Kondo Seiichi

机构信息

Department of Microbiology, School of Pharmaceutical Sciences, Josai University, Sakado, Saitama 350-0295, Japan.

出版信息

Carbohydr Res. 2003 May 1;338(10):1055-62. doi: 10.1016/s0008-6215(03)00077-6.

Abstract

Lipopolysaccharides (LPS) of Vibrio parahaemolyticus O2 and O-untypable (OUT) strain (KX-V212) isolated from an individual patient were shown to contain 5,7-diamino-3,5,7,9-tetradeoxy-non-2-ulosonic acid (NonlA), which was readily released from LPS by mild acid hydrolysis. In the present study, we investigated the chemical and serological properties of NonlA isolated from LPS of V. parahaemolyticus O2 and OUT KX-V212. GC-MS and NMR analysis identified the NonlA from LPS of O2 to be 5,7-diacetamido-3,5,7,9-tetradeoxy-D-glycero-D-galacto-non-2-ulosonic acid (5NAc7NAcNonlA) and that from LPS of KX-V212 to be 5-acetamido-7-(N-acetyl-D-alanyl)amido-3,5,7,9-tetradeoxy-D-glycero-D-galacto-non-2-ulosonic acid (5NAc7NAlaNAcNonlA). In ELISA inhibition analysis, 5NAc7NAcNonlA inhibited the O2 LPS/anti-O2 antiserum system, whereas, 5NAc7NAlaNAcNonlA did not show any inhibitory activity. However, after N-deacylation of 5NAc7NAlaNAcNonlA followed by N-acetylation, the product (5NAc7NAcNonlA) inhibited the O2 LPS/anti-O2 antiserum system to the same extent as that of 5NAc7NAcNonlA obtained from O2 LPS. These results suggest that 5NAc7NAcNonlA might be related to the serological specificity of O2 LPS as one of main epitope(s) involved in O2 LPS.

摘要

从一名个体患者分离出的副溶血性弧菌O2和不可分型(OUT)菌株(KX-V212)的脂多糖(LPS)显示含有5,7-二氨基-3,5,7,9-四脱氧壬-2-酮糖酸(NonlA),其通过温和酸水解可从LPS中轻易释放出来。在本研究中,我们研究了从副溶血性弧菌O2和OUT KX-V212的LPS中分离出的NonlA的化学和血清学特性。气相色谱-质谱联用(GC-MS)和核磁共振(NMR)分析确定,O2 LPS中的NonlA为5,7-二乙酰氨基-3,5,7,9-四脱氧-D-甘油-D-半乳糖壬-2-酮糖酸(5NAc7NAcNonlA),而KX-V212 LPS中的NonlA为5-乙酰氨基-7-(N-乙酰-D-丙氨酰基)氨基-3,5,7,9-四脱氧-D-甘油-D-半乳糖壬-2-酮糖酸(5NAc7NAlaNAcNonlA)。在酶联免疫吸附测定(ELISA)抑制分析中,5NAc7NAcNonlA抑制O2 LPS/抗O2抗血清系统,而5NAc7NAlaNAcNonlA未显示任何抑制活性。然而,5NAc7NAlaNAcNonlA进行N-脱酰化后再进行N-乙酰化,产物(5NAc7NAcNonlA)对O2 LPS/抗O2抗血清系统的抑制程度与从O2 LPS获得的5NAc7NAcNonlA相同。这些结果表明,5NAc7NAcNonlA可能作为O2 LPS中涉及的主要表位之一与O2 LPS的血清学特异性相关。

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