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通过分析包含rRNA顺反子的DNA限制性片段长度多态性检测斯氏普罗威登斯菌临床分离株中的基因组变异。

Detection of genomic variation in Providencia stuartii clinical isolates by analysis of DNA restriction fragment length polymorphisms containing rRNA cistrons.

作者信息

Owen R J, Beck A, Dayal P A, Dawson C

机构信息

National Collection of Type Cultures, Central Public Health Laboratory, London, United Kingdom.

出版信息

J Clin Microbiol. 1988 Oct;26(10):2161-6. doi: 10.1128/jcm.26.10.2161-2166.1988.

Abstract

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.

摘要

对主要从英国医院分离出的26株斯氏普罗威登斯菌的染色体DNA以及斯氏普罗威登斯菌、鲁氏普罗威登斯菌和普通变形杆菌的参考菌株,用限制性内切酶EcoRI和HindIII进行消化。在琼脂糖凝胶中进行电泳后,将片段与用斯氏普罗威登斯菌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,被用作衡量种内和种间微小基因组变异的指标。斯氏普罗威登斯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存在一些异质性,EcoRI消化比HindIII能更好地区分菌株。这种rDNA指纹图谱由5至7条带组成,大小在5至28千碱基范围内。通过数值分析比较了11种不同的EcoRI模式,并鉴定出几个菌株组或亚组。超过一半(26株中的15株)的脲酶阴性分离株(Aa和Ab亚组)的模式仅因一条25千碱基带的有无而不同。来自其他临床材料的脲酶阴性菌株在模式上更具异质性。菌株模式组与脲酶产生或分离株的地理位置之间没有明显的相关性。斯氏普罗威登斯菌的rDNA指纹图谱与相关的普罗威登斯菌和变形杆菌物种的指纹图谱有很大不同,并且比总DNA消化更能敏感地检测到微小的基因组差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b251/266837/3a83dcde7020/jcm00082-0267-a.jpg

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