首页> 外文期刊>Journal of Clinical Microbiology >Comparative evaluation of molecular typing of strains from a national epidemic due to Salmonella brandenburg by rRNA gene and IS200 probes and pulsed-field gel electrophoresis.
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Comparative evaluation of molecular typing of strains from a national epidemic due to Salmonella brandenburg by rRNA gene and IS200 probes and pulsed-field gel electrophoresis.

机译:通过rRNA基因和IS200探针以及脉冲场凝胶电泳比较评估勃兰登堡沙门氏菌引起的全国流行菌株的分子分型。

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In Switzerland in 1992 there was a prolonged series of outbreaks of human salmonellosis caused by a previously rare serotype, Salmonella brandenburg. In order to examine the genotypic basis of the epidemic, molecular typing was applied to representative strains of this serovar isolated between 1983 and 1992. These included sporadic human isolates up to 1985, isolates from unrelated geographical areas, and Swiss isolates from humans, animals, and meat products isolated after 1991. Plasmid profiling was not found to be applicable to S. brandenburg, but chromosomal typing was accomplished by analyzing restriction fragment length polymorphisms with DNA probes for three marker loci; the 16S and 23S rRNA genes and sites of insertion of the mobile DNA element IS200. The macrorestriction profiles of the whole genome were examined by pulsed-field gel electrophoresis, which proved to be the most discriminatory of the typing methods. The study demonstrated the comparative value and complementary relationship between these typing methods for epidemiological purposes. All approaches concurred in identifying the 1992 isolates as a single genotypic clone, which was present in multiple (food) vehicles of infection. They were distinct from sporadic isolates of this serovar and from strains of S. brandenburg isolated in other countries.
机译:1992年在瑞士,由以前罕见的血清型勃兰登堡沙门氏菌引起的人类沙门氏菌病暴发时间较长。为了检查该流行病的基因型基础,将分子分型应用于该血清型的代表性菌株,此菌株在1983年至1992年之间分离。这些菌株包括直至1985年的零星人类分离株,不相关地理区域的分离株以及瑞士人类,动物,未发现质粒图谱适用于勃兰登堡链球菌,但在1991年之后分离出肉制品。但是,通过使用DNA探针分析三个标记位点的限制性片段长度多态性来完成染色体分型。 16S和23S rRNA基因以及可移动DNA元件IS200的插入位点。通过脉冲场凝胶电泳检查了整个基因组的宏观限制性图谱,这被证明是最有区别的打字方法。该研究证明了这些打字方法在流行病学方面的比较价值和互补关系。所有方法都同意将1992年的分离株鉴定为单个基因型克隆,该克隆存在于多种(食物)感染媒介中。它们与该血清型的零星分离株以及在其他国家分离的勃兰登堡链球菌菌株不同。

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