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首页> 外文期刊>Journal of Clinical Microbiology >On the nature and use of randomly amplified DNA from Staphylococcus aureus.
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On the nature and use of randomly amplified DNA from Staphylococcus aureus.

机译:金黄色葡萄球菌随机扩增DNA的性质和用途。

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Various DNA-based methods have been introduced to genetically type Staphylococcus aureus strains but not a single technique is universally applicable. In order to search for DNA probes suitable for differentiating strains, randomly amplified polymorphic DNA patterns were generated for 243 S. aureus strains and a single isolate of Staphylococcus intermedius. All fingerprints were examined for unique amplicons, and the nature of 42 of these DNA fragments was investigated. Partial DNA sequences were determined, and several homologies were discovered with known S. aureus sequences (plasmid pSH6 DNA with insertion sequences, agrA and agrB sequences, hld genes, the gene for 23S rRNA, the lysyl tRNA synthetase gene, and the threonyl tRNA synthetase gene) and with genes from other species (Haemophilus influenzae bexA and Bacillus subtilis spoF and ctrA). Thirty fragments were of previously unknown origin. In Southern blots containing Eco RI-digested DNA from S. aureus strains and the S. intermedius strain, nine probes demonstrated the capacity to differentiate strains on the basis of the presence or absence of the sequence element in the staphylococcal genome involved. The remainder of the probes displayed restriction fragment length polymorphisms (n = 12), hybridized in a homogeneously positive fashion (n = 13) or hybridized only with their source strains (n = 8) (four of the latter were specific to S. intermedius). Three of the nine strain-specific probes were overlapping, and two of the others were found to display a high level of inconsistency among epidemiologically related strains. Thus, five strain-specific probes remained that, in a 5-digit typing system, accurately distinguished epidemiologically related and unrelated strains of S. aureus. We conclude that application of strain-specific DNA probes, selected on the basis of differing randomly amplified polymorphic DNA patterns, promises to become a technically simple, robust, and reproducible tool that may significantly facilitate the study of the epidemiology of S. aureus infections.
机译:已经将多种基于DNA的方法引入到金黄色葡萄球菌菌株的遗传类型中,但是没有一种技术可以普遍应用。为了搜索适合于区分菌株的DNA探针,针对243个金黄色葡萄球菌菌株和中间葡萄球菌的单个分离物产生了随机扩增的多态DNA模式。检查了所有指纹的独特扩增子,并研究了其中42个DNA片段的性质。确定了部分DNA序列,并发现了与已知金黄色葡萄球菌序列(具有插入序列,agrA和agrB序列的质粒pSH6 DNA,hld基因,23S rRNA基因,赖氨酰tRNA合成酶基因和苏氨酰tRNA合成酶的几种同源性)基因)和其他物种的基因(流感嗜血杆菌bexA和枯草芽孢杆菌spoF和ctrA)。三十个碎片以前未知来源。在含有来自金黄色葡萄球菌菌株和中间链球菌菌株的Eco RI消化的DNA的Southern印迹中,九种探针证明了根据所涉及的葡萄球菌基因组中序列元素的存在与否,能够区分菌株。其余的探针显示限制性片段长度多态性(n = 12),以均相阳性方式杂交(n = 13)或仅与其来源菌株杂交(n = 8)(后者中的四个对中间链球菌有特异性) )。九个菌株特异性探针中的三个重叠,另外两个在流行病学相关菌株中显示出高度的不一致。因此,剩下的五种菌株特异性探针在5位数字分型系统中可以准确地区分金黄色葡萄球菌的流行病学相关和不相关菌株。我们得出的结论是,基于不同的随机扩增多态性DNA模式选择的菌株特异性DNA探针的应用有望成为技术上简单,可靠且可重现的工具,可能会大大促进金黄色葡萄球菌感染的流行病学研究。

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