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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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摘要

The stx-flanking regions of 49 Shiga toxin-producing Escherichia coli strains and nine Shigella dysenteriae serotype 1 strains containing either stx, stx1, stx2, or stx2 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 of stx1-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 in stx1-harboring E. coli O111:H− strains. Stx2-producing E. coli strains revealed amplification products of different lengths and restriction patterns, suggesting greater heterogeneity than in stx1-positive strains. We also obtained specific PCR products for two Stx2c-producing and seven Stx2f-producing E. 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 stx genes of all strains investigated are continuous with phage sequences. Whereas almost all strains except E. coli O111: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 the stx-flanking regions is similar in all strains investigated, whereas fine-structure analysis showed subtle differences among the sequences examined. Our results support the hypothesis that stx genes in E. coli and S. dysenteriae are generally phage-borne.
机译:检查了49个产志贺毒素的大肠杆菌菌株和9个含有stx,stx1,stx2或stx2变异基因的痢疾志贺氏菌血清型1菌株的stx侧翼区域。我们使用一组引物对这些区域进行PCR分析,引物具有一个对各个stx基因具有特异性的引物和一个与Stx噬菌体H-19B和933W的序列互补的第二个引物。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。 O157,O26和0103血清群的含stx1大肠杆菌菌株的PCR产物显示相同的长度和相似的限制模式。但是,我们未能在携带stx1的大肠杆菌O111:H-菌株中扩增3'stx侧翼区域。产生Stx2的大肠杆菌菌株显示出不同长度和限制模式的扩增产物,表明其异质性比stx1阳性菌株更大。我们还获得了针对两个产生Stx2c和七个产生Stx2f的大肠杆菌菌株进行PCR分析时的特异性PCR产物。在9株痢疾链球菌1型菌株中,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。尽管除大肠杆菌O111:H-菌株外几乎所有菌株均与S样基因相关,但在9株痢疾链球菌1型菌株和3株大肠杆菌中均未证明与Q的相关性。此外,我们显示,在所有研究的菌株中,stx侧翼区域的组织均相似,而精细结构分析显示,所检查序列之间存在细微差异。我们的结果支持这样的假设,即大肠杆菌和痢疾链球菌中的stx基因通常是噬菌体传播的。

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