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Type IV O antigen modification genes in the genome of Shigella flexneri NCTC 8296

机译:IV型抗原修饰基因在肖格氏菌·柔屈NCTC 8296的基因组中

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The genes encoding type IV O antigen glucosylation were characterized from both Escherichia coli and Shigella flexneri. The putative O antigen modification genes from E. coli, o120 o306 o443, were PCR-amplified and introduced into S. flexneri serotype Y strain SFL124. Immunogold labelling and phage sensitivity indicated the presence of both serotype Y and serotype 4a O antigens on the cell surface of the resulting recombinant SFL124 strains, suggesting that only partial serotype conversion was conferred by the E. coli genes. The type IV O antigen modification genes were then isolated and characterized from S. flexneri serotype 4a strain NCTC 8296. A 3·8?kb chromosomal fragment conferred complete conversion to serotype 4a when introduced into SFL124. Sequence analysis of the fragment revealed the presence of three genes, gtrAIVgtrBIVgtrIVSf. DNAs homologous to bacteriophage int and attP were located upstream of gtrAIV, suggesting that this region of the NCTC 8296 genome may have originated from a bacteriophage; however, a serotype-converting phage could not be induced from this strain nor from other strains used in this study. Comparison of the GtrIVSf and GtrIVEc (o443) proteins revealed that they are 41% identical and 63% similar, which is the highest degree of similarity reported among the S. flexneri O antigen glucosyltransferases.
机译:编码IV型抗原葡萄糖化的基因是从大肠杆菌和谢氏菌·柔屈的表征。来自大肠杆菌O120 O306 O443的推定的O抗原修饰基因被PCR扩增并引入S.Flexneri血清型Y菌株SFL124中。免疫角质标记和噬菌体敏感性表明,在所得重组SFL124菌株的细胞表面上存在血清型Y和血清型4A抗原,表明仅通过大肠杆菌基因赋予部分血清型转化。然后分离IV型抗原改性基因并用S.Flexeri血清型4A菌株NCTC 8296表征。3·8?KB染色体片段在引入SFL124时赋予血清型4a完全转化为血清型4a。片段的序列分析显示出三种基因的存在,GtraivGtbivgtrivsf。与噬菌体INT和ATTP同源的DNA位于GTRAIV的上游,表明NCTC 8296基因组的该区域可能来自噬菌体;然而,不能从该菌株诱导血清型转化噬菌体,也不能从本研究中使用的其他菌株诱导。 GTRIVSF和GTRIVEC(O443)蛋白的比较显示,它们具有41%相同,63%相似,这是S.Flexeri o抗原葡萄糖酰基转移酶中报道的最高相似性。

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