首页> 外文期刊>Advances in Experimental Medicine and Biology >The Type I Restriction Enzymes as Barriers to Horizontal Gene Transfer: Determination of the DNA Target Sequences Recognised by Livestock-Associated Methicillin-Resistant Staphylococcus aureus Clonal Complexes 133/ST771 and 398
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The Type I Restriction Enzymes as Barriers to Horizontal Gene Transfer: Determination of the DNA Target Sequences Recognised by Livestock-Associated Methicillin-Resistant Staphylococcus aureus Clonal Complexes 133/ST771 and 398

机译:I型限制酶作为水平基因转移的障碍:牲畜相关的耐甲氧西林金黄色葡萄球菌克隆复合体133 / ST771和398识别的DNA目标序列的确定

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The Type I DNA restriction-modification (RM) systems of Staphylococcus aureus are known to act as a significant barrier to horizontal gene transfer between S. aureus strains belonging to different clonal complexes. The livestock-associated clonal complexes CC133/771 and CC398 contain Type I RM systems not found in human MRSA strains as yet but at some point transfer will occur. When this does take place, horizontal gene transfer of resistance will happen more easily between these strains. The reservoir of antibiotic resistance, virulence and host-adaptation genes present in livestock-associated MRSA will then potentially contribute to the development of newly evolving MRSA clones. The target sites recognised by the Type I RM systems of CC133/771 and CC398 were identified as CAG(N)_5RTGA and ACC(N)_5RTGA, respectively. Assuming that these enzymes recognise the methylation state of adenine, the underlined A and T bases indicate the unique positions of methylation. Target methylation points for enzymes from CC1 were also identified. The methylation points for CC1-1 are CCAY(N)_5TTAA and those for CC1-2 are CCAY(N)_6TGT with the underline indicating the adenine methylation site thus clearing up the ambiguity noted previously (Roberts et al. 2013, Nucleic Acids Res 41:7472-7484) for the half sites containing two adenine bases.
机译:已知金黄色葡萄球菌的I型DNA限制性修饰(RM)系统可作为对属于不同克隆复合体的金黄色葡萄球菌菌株之间水平基因转移的重要屏障。与牲畜相关的克隆复合物CC133 / 771和CC398包含人MRSA菌株中尚未发现的I型RM系统,但在某些时候会发生转移。当发生这种情况时,在这些菌株之间将更容易发生抗药性的水平基因转移。与牲畜相关的MRSA中存在的抗生素抗性,毒力和宿主适应性基因的库将潜在地促进新进化的MRSA克隆的发展。 CC133 / 771和CC398的I型RM系统识别的目标站点分别被标识为CAG(N)_5RTGA和ACC(N)_5RTGA。假设这些酶识别腺嘌呤的甲基化状态,带下划线的A和T碱基表示甲基化的独特位置。还确定了来自CC1的酶的目标甲基化点。 CC1-1的甲基化点为CCAY(N)_5TTAA,CC1-2的甲基化点为CCAY(N)_6TGT,下划线表示腺嘌呤甲基化位点,从而消除了先前提到的歧义(Roberts等,2013,Nucleic Acids Res 41:7472-7484)包含两个腺嘌呤碱基的半位点。

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