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首页> 外文期刊>Infection and immunity >Structural Analysis of Phage-Borne stx Genes and Their Flanking Sequences in Shiga Toxin-Producing Escherichia coli and Shigella dysenteriae Type 1 Strains
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Structural Analysis of Phage-Borne stx Genes and Their Flanking Sequences in Shiga Toxin-Producing Escherichia coli and Shigella dysenteriae Type 1 Strains

机译:产志贺毒素的大肠杆菌和痢疾志贺氏菌1型菌株噬菌体stx基因及其侧翼序列的结构分析

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The stx-flanking regions of 49 Shiga toxin-producingEscherichia coli strains and nine Shigella dysenteriae serotype 1 strains containing either stx,stx 1, stx 2, orstx 2 variant genes, were examined. We analyzed these regions by PCR using a set of primers with one primer specific for the respective stx gene and a second primer complementary to sequences of Stx phages H-19B and 933W. We further characterized the amplification products by restriction endonuclease digestion and nucleotide sequencing. PCR products ofstx 1-containing E. coli strains of serogroups O157, O26, and 0103 showed the same lengths and similar restriction patterns. However, we failed to amplify the 3′stx-flanking region instx 1-harboring E. coliO111:H? strains. Stx2-producing E. colistrains revealed amplification products of different lengths and restriction patterns, suggesting greater heterogeneity than instx 1-positive strains. We also obtained specific PCR products for two Stx2c-producing and seven Stx2f-producingE. coli strains when they were subjected to PCR analysis. In nine S. dysenteriae type 1 strains, H-19B- and 933W-specific primers amplified only the 3′ stx-flanking region. The results of our study demonstrate that the stxgenes of all strains investigated are continuous with phage sequences. Whereas almost all strains except E. coliO111:H? strains were associated with a S-like gene, association with Q could not be demonstrated in nine S. dysenteriae type 1 strains and three E. coli strains. Furthermore, we showed that the organization of thestx-flanking regions is similar in all strains investigated, whereas fine-structure analysis showed subtle differences among the sequences examined. Our results support the hypothesis thatstx genes in E. coli and S. dysenteriae are generally phage-borne.
机译:产志贺毒素的49株大肠杆菌和9株含有 stx的痢疾志贺氏菌血清型1株的 stx 侧翼区。 em>, stx 1 stx 2 stx 2 变异基因。我们使用一组引物对这些区域进行了PCR分析,其中一个引物对各个 stx 基因具有特异性,第二个引物与Stx噬菌体H-19B和933W的序列互补。我们通过限制性核酸内切酶消化和核苷酸测序进一步表征了扩增产物。包含 stx 1 E的PCR产物。 O157,O26和0103血清群的大肠杆菌菌株显示相同的长度和相似的限制模式。然而,我们未能扩增出 stx 1 -携带 E的3' stx 侧翼区域。大肠杆菌 O111:H ?菌株。产生Stx2的 E。大肠埃希菌菌株显示出不同长度和限制性图谱的扩增产物,表明其异质性高于 stx 1 阳性菌株。我们还获得了两个产生Stx2c和七个产生Stx2f的E的特异性PCR产物。菌株进行PCR分析时。在九个 S。痢疾1型菌株,H-19B和933W特异性引物仅扩增3' stx 侧翼区域。我们的研究结果表明,所研究的所有菌株的 stx 基因均与噬菌体序列连续。而除 E外几乎所有菌株。大肠杆菌O111:H ?菌株与S样基因相关,在9个 S中无法证明与Q的相关性。痢疾 1型菌株和3株 E。大肠杆菌菌株。此外,我们表明,在所有所研究的菌株中, stx -侧翼区域的组织都是相似的,而精细结构分析显示,所检验的序列之间存在细微的差异。我们的结果支持 E中的 stx 基因的假设。大肠菌 S。痢疾一般由噬菌体传播。

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