Gozdziewicz Tomasz K, Man-Kupisinska Aleksandra, Lugowski Czesław, Lukasiewicz Jolanta
Department of Immunochemistry, Ludwik Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, R. Weigla 12, PL-53-114 Wroclaw, Poland; Department of Biotechnology, Mass Spectrometry Laboratory, Wroclaw Research Center EIT+, Stablowicka 147, PL-54-066 Wroclaw, Poland.
Department of Immunochemistry, Ludwik Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, R. Weigla 12, PL-53-114 Wroclaw, Poland.
Carbohydr Res. 2015 May 18;408:119-26. doi: 10.1016/j.carres.2014.11.017. Epub 2014 Dec 3.
Endotoxins (lipopolysaccharides, LPS) are the main surface antigens and virulence factors of Gram-negative bacteria involved for example in the development of nosocomial infections and sepsis. They consist of three main regions: O-specific polysaccharide, core oligosaccharide, and lipid A. Bacteria modify LPS structure to escape the immune defence, but also to adapt to environmental conditions. LPS's structures are highly diversified in the O-specific polysaccharide region to evade bactericidal factors of immune system, but retain some common epitopes that are potential candidates for therapeutic strategies against bacterial infections. Common occurrence of glycine within the structure of LPS is a known phenomenon and was previously reported for variety of species. Since glycine residue substitutes mainly core oligosaccharide of LPS, especially inner core region, it was also considered as a part of common epitope for broad-reactive antimicrobial antibodies. Herein, we used multiple-stage electrospray ionisation mass spectrometry to identify glycine substitution in core oligosaccharide type characteristic for Hafnia alvei LPS, and isolated from five strains of different O-serotypes: 32, PCM 1190, PCM 1192, PCM 1200, and PCM 1209. The location of glycine in core oligosaccharide was determined in detail for LPS 1190 using ESI-MS(n). Three glycoforms were identified, including two mono-glycinylated and one diglycinylated core oligosaccharides.
内毒素(脂多糖,LPS)是革兰氏阴性菌的主要表面抗原和毒力因子,例如参与医院感染和败血症的发生。它们由三个主要区域组成:O-特异性多糖、核心寡糖和脂质A。细菌会改变LPS结构以逃避免疫防御,同时也适应环境条件。LPS的结构在O-特异性多糖区域高度多样化,以逃避免疫系统的杀菌因子,但保留了一些常见表位,这些表位是针对细菌感染治疗策略的潜在候选物。LPS结构中普遍存在甘氨酸是一个已知现象,此前已在多种物种中报道。由于甘氨酸残基主要取代LPS的核心寡糖,尤其是内核区域,它也被认为是广泛反应性抗菌抗体共同表位的一部分。在此,我们使用多阶段电喷雾电离质谱法来鉴定 Hafnia alvei LPS特征性核心寡糖类型中的甘氨酸取代情况,该LPS从五株不同O-血清型(32、PCM 1190、PCM 1192、PCM 1200和PCM 1209)中分离得到。使用ESI-MS(n)详细确定了LPS 1190中甘氨酸在核心寡糖中的位置。鉴定出三种糖型,包括两种单甘氨酸化和一种双甘氨酸化的核心寡糖。