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Design and evaluation of PCR primers which differentiate Escherichia coli O157:H7 and related serotypes

机译:区分大肠杆菌O157:H7和相关血清型的PCR引物的设计和评估

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AIMS: To develop methods to differentiate Escherichia coli O157:H7 and related serotypes by the use of amplicon length polymorphism (ALP) analysis based on identifying DNA sequence deletions within highly homologous regions of three sequenced E. coli strains. METHODS AND RESULTS: Potential primer locations along the ancestral genomic backbone were identified and evaluated against three sequenced genomes and then applied to a reference set of pathogenic E. coli strains. All 16 primer combinations generated the expected diagnostic fragments as predicted for the E. coli K12 MG1655, O157:H7 EDL933, and O157:H7B Sakai genomes. CONCLUSIONS: This study defines a collection of primers distributed along the length of the E. coli genome that were applied to ALP analysis methods to successfully differentiate between serotypes of E. coli O157:H7 and other E. coli serotypes. SIGNIFICANCE AND IMPACT OF THE STUDY: ALP-PCR analysis method was validated as an independent method of classification when compared with that of rep-PCR. The principles underlying ALP analysis can be readily applied for the detection and differentiation of other closely related microbial species because of the abundance of complete DNA sequence data for a large number of microbial genomes.
机译:目的:通过基于三个测序大肠杆菌菌株高度同源区域内DNA序列缺失的扩增子长度多态性(ALP)分析,开发区分大肠杆菌O157:H7和相关血清型的方法。方法和结果:沿着祖先的基因组骨架确定了潜在的引物位置,并针对三个测序的基因组进行了评估,然后将其应用于一组病原性大肠杆菌菌株参考中。如对大肠杆菌K12 MG1655,O157:H7 EDL933和O157:H7B Sakai基因组所预测的,所有16种引物组合均产生了预期的诊断片段。结论:本研究定义了沿大肠杆菌基因组长度分布的引物集合,这些引物已用于ALP分析方法,以成功地区分大肠杆菌O157:H7血清型和其他大肠杆菌血清型。研究的意义和影响:与rep-PCR相比,ALP-PCR分析方法被确认为一种独立的分类方法。由于大量微生物基因组的完整DNA序列数据丰富,ALP分析的基本原理可轻松应用于其他密切相关的微生物物种的检测和区分。

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