首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Detection of genomic variation in Providencia stuartii clinical isolates by analysis of DNA restriction fragment length polymorphisms containing rRNA cistrons.
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Detection of genomic variation in Providencia stuartii clinical isolates by analysis of DNA restriction fragment length polymorphisms containing rRNA cistrons.

机译:通过分析含有rRNA顺反子的DNA限制性片段长度多态性检测斯氏普罗维登斯氏菌临床分离株的基因组变异。

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摘要

Chromosomal DNA from 26 strains of Providencia stuartii isolated mainly in hospitals in the United Kingdom and reference strains of P. stuartii, P. rustigianii, and Proteus vulgaris were digested with the restriction endonucleases EcoRI and HindIII. After electrophoresis in agarose gels, the fragments were subjected to Southern blot hybridization analysis with a biotin-labeled cDNA probe transcribed from a mixture of 16S and 23S rRNA from P. stuartii NCTC 11800T. The pattern of bands (the rDNA fingerprint), which depended on restriction fragment length polymorphisms containing rRNA genes, was used as a measure of minor genomic variation within and between species. The P. stuartii clinical isolates had similar total digest patterns, but the rDNA fingerprints revealed some heterogeneity between strains, with EcoRI digests providing better strain discrimination than HindIII. Such rDNA fingerprints comprised between five and seven bands with sizes in the range of 5 to 28 kilobases. The 11 different EcoRI patterns were compared by numerical analysis, and several groups or subgroups of strains were identified. Over half (15 of 26) of the urease-negative isolates (subgroups Aa and Ab) had patterns that differed only by the presence or absence of a 25-kilobase band. Urease-negative strains from other clinical material were more heterogeneous in their patterns. No correlation was apparent between strain pattern group and urease production or geographic location of isolate. The P. stuartii rDNA fingerprints were quite distinct from those of allied Providencia and Proteus species and provided a more sensitive measure of minor genomic differences than total DNA digests did.
机译:使用限制性内切核酸酶EcoRI和HindIII消化了主要在英国的医院中分离的26株普罗维登斯氏普罗维登斯氏菌菌株的染色体DNA,以及普氏疟原虫,锈病锈菌和变形杆菌的参考菌株。在琼脂糖凝胶上电泳后,将片段用从斯图亚特氏菌NCTC 11800T的16S和23S rRNA混合物转录的生物素标记的cDNA探针进行Southern印迹杂交分析。条带的模式(rDNA指纹图谱)取决于包含rRNA基因的限制性片段长度多态性,用于衡量物种内部和物种之间较小的基因组变异。斯氏假单胞菌临床分离株具有相似的总消化模式,但rDNA指纹图谱显示菌株之间有些异质性,EcoRI消化比HindIII更好地区分了菌株。此类rDNA指纹包括5至7条带,大小范围为5至28 KB。通过数值分析比较了11种不同的EcoRI模式,并鉴定了几组菌株或亚组。超过一半(26个中的15个)的脲酶阴性分离株(亚群Ab和亚群Ab)的模式仅因存在或不存在25碱基碱基带而不同。来自其他临床材料的脲酶阴性菌株在其模式上更加异质。菌株模式组与脲酶生产或分离物地理位置之间没有明显的相关性。 P. stuartii rDNA指纹图与盟约Providencia和Proteus物种的指纹图谱非常不同,并且比总DNA消化产物更敏感地测量了微小的基因组差异。

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