Whitfield Chris, Kaniuk Natalia, Frirdich Emilisa
Department of Microbiology, University of Guelph, Guelph, Ontario, Canada.
J Endotoxin Res. 2003;9(4):244-9. doi: 10.1179/096805103225001440.
In the Enterobacteriaceae, the core oligosaccharide provides the junction between the highly conserved lipid A and the remarkably diverse polysaccharide O antigen. The basic structure of the inner (lipid A-proximal) core is well conserved, perhaps reflecting constraints imposed by its involvement in the structural integrity of the outer membrane. However, non-stoichiometric modifications do create some structural variants. The outer core may show more variation. Efforts to develop immunoprophylactic strategies based on the core oligosaccharide require a detailed understanding of core immunochemistry, the accessibility of specific epitopes in the LPS, and the distribution of specific structures within natural populations. The availability of sequences for the waa (core biosynthesis) loci and functional data for the gene products provide a molecular basis for the known structural diversity in Escherichia coli and Salmonella core oligosaccharide. Surveys of waa-locus organization have established the distribution of these core types in natural populations and have identified genetic variants that provide candidates for additional novel structures.
在肠杆菌科中,核心寡糖提供了高度保守的脂多糖A与极为多样的多糖O抗原之间的连接。内部(靠近脂多糖A)核心的基本结构高度保守,这可能反映出其参与外膜结构完整性所带来的限制。然而,非化学计量修饰确实会产生一些结构变体。外部核心可能表现出更多的变异性。基于核心寡糖开发免疫预防策略需要详细了解核心免疫化学、脂多糖中特定表位的可及性以及自然群体中特定结构的分布。 waa(核心生物合成)基因座的序列可用性以及基因产物的功能数据为大肠杆菌和沙门氏菌核心寡糖中已知的结构多样性提供了分子基础。对waa基因座组织的调查确定了这些核心类型在自然群体中的分布,并鉴定出了可为其他新型结构提供候选的遗传变体。