Drummelsmith J, Amor P A, Whitfield C
Department of Microbiology, University of Guelph, Ontario, Canada.
J Bacteriol. 1997 May;179(10):3232-8. doi: 10.1128/jb.179.10.3232-3238.1997.
Individual Escherichia coli strains produce several cell surface polysaccharides. In E. coli E69, the his region of the chromosome contains the rfb (serotype O9 lipopolysaccharide O-antigen biosynthesis) and cps (serotype K30 group IA capsular polysaccharide biosynthesis) loci. Polymorphisms in this region of the Escherichia coli chromosome reflect extensive antigenic diversity in the species. Previously, we reported a duplication of the manC-manB genes, encoding enzymes involved in GDP-mannose formation, upstream of rfb in strain E69 (P. Jayaratne et al., J. Bacteriol. 176:3126-3139, 1994). Here we show that one of the manC-manB copies is flanked by IS1 elements, providing a potential mechanism for the gene duplication. Adjacent to manB1 on the IS1-flanked segment is a further open reading frame (ugd), encoding uridine-5'-diphosphoglucose dehydrogenase. The Ugd enzyme is responsible for the production of UDP-glucuronic acid, a precursor required for K30 antigen synthesis. Construction of a chromosomal ugd::Gm(r) insertion mutation demonstrated the essential role for Ugd in the biosynthesis of the K30 antigen and confirmed that there is no additional functional ugd copy in strain E69. PCR amplification and Southern hybridization were used to examine the distribution of IS1 elements and ugd genes in the vicinity of rfb in other E. coli strains, producing different group IA K antigens. The relative order of genes and, where present, IS1 elements was established in these strains. The regions adjacent to rfb in these strains are highly variable in both size and gene order, but in all cases where a ugd homolog was present, it was found near rfb. The presence of IS1 elements in the rfb regions of several of these strains provides a potential mechanism for recombination and deletion events which could contribute to the antigenic diversity seen in surface polysaccharides.
单个大肠杆菌菌株可产生多种细胞表面多糖。在大肠杆菌E69中,染色体的his区域包含rfb(O9型脂多糖O抗原生物合成)和cps(K30型IA族荚膜多糖生物合成)基因座。大肠杆菌染色体该区域的多态性反映了该物种广泛的抗原多样性。此前,我们报道了在菌株E69中,编码参与GDP-甘露糖形成的酶的manC-manB基因在rfb上游发生了重复(P. Jayaratne等人,《细菌学杂志》176:3126 - 3139,1994年)。在此我们表明,manC-manB的一个拷贝两侧是IS1元件,这为基因重复提供了一种潜在机制。在IS1侧翼片段上与manB1相邻的是另一个开放阅读框(ugd),编码尿苷-5'-二磷酸葡萄糖脱氢酶。Ugd酶负责产生UDP-葡萄糖醛酸,这是K30抗原合成所需的前体。构建染色体ugd::Gm(r)插入突变证明了Ugd在K30抗原生物合成中的关键作用,并证实菌株E69中不存在额外的功能性ugd拷贝。使用PCR扩增和Southern杂交来检测其他产生不同IA族K抗原的大肠杆菌菌株中rfb附近IS1元件和ugd基因的分布。确定了这些菌株中基因以及(若存在)IS1元件的相对顺序。这些菌株中与rfb相邻的区域在大小和基因顺序上高度可变,但在所有存在ugd同源物的情况下,都在rfb附近发现。这些菌株中几个菌株的rfb区域存在IS1元件,为重组和缺失事件提供了一种潜在机制,这可能导致表面多糖中出现的抗原多样性。