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噬菌体抗性铜绿假单胞菌PAO1突变体中脂多糖的精细结构分析

Fine structure analysis of lipopolysaccharides in bacteriophage-resistant Pseudomonas aeruginosa PAO1 mutants.

作者信息

Latino Libera, Caroff Martine, Pourcel Christine

机构信息

Institute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Univ Paris-Sud, Université Paris-Saclay, 91198 Gif-sur-Yvette cedex, France.

LPS-BioSciences, Bât 409, I2BC, Université Paris-Sud, 91405 Orsay, France.

出版信息

Microbiology (Reading). 2017 Jun;163(6):848-855. doi: 10.1099/mic.0.000476.

Abstract

Pseudomonas aeruginosa lipopolysaccharides (LPS) serve as primary receptors for many bacteriophages and, consequently, their biosynthesis is frequently affected in phage-resistant mutants. We previously isolated phage-resistant PAO1 mutants using three different phages, and showed that they were affected in the synthesis of LPS. Here we have investigated in detail the effect of mutations in seven genes involved in different steps of the production of core and oligosaccharide chains. The band profile of purified LPS was analysed by PAGE, and we further characterized the O-chains and core structures by MALDI mass spectrometry (MS). Mild LPS extraction conditions and native LPS MS analyses helped unveil lipid A molecular species with three phosphate residues in the close vicinity of the already highly charged inner-core region. No other MS direct analysis has allowed this peculiarity to be demonstrated for native lipid A high-molecular-weight molecular species, in normal growth conditions and without involving separation techniques. The present results shed light on the possible interactions between the phages and the LPS structures in the early phase of infection.

摘要

铜绿假单胞菌脂多糖(LPS)是许多噬菌体的主要受体,因此,其生物合成在噬菌体抗性突变体中经常受到影响。我们之前使用三种不同的噬菌体分离出了噬菌体抗性PAO1突变体,并表明它们在LPS合成中受到影响。在这里,我们详细研究了参与核心和寡糖链生产不同步骤的七个基因中的突变效应。通过PAGE分析纯化LPS的条带图谱,并通过基质辅助激光解吸电离质谱(MALDI-MS)进一步表征O链和核心结构。温和的LPS提取条件和天然LPS MS分析有助于揭示在已经高度带电的内核区域附近具有三个磷酸残基的脂多糖分子种类。在正常生长条件下且不涉及分离技术的情况下,没有其他MS直接分析能够证明天然脂多糖高分子量分子种类的这种特性。目前的结果揭示了感染早期噬菌体与LPS结构之间可能的相互作用。

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