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利用rRNA基因和IS200探针以及脉冲场凝胶电泳对来自一起由勃兰登堡沙门氏菌引起的全国性疫情的菌株进行分子分型的比较评估。

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.

作者信息

Baquar N, Burnens A, Stanley J

机构信息

Molecular Genetics Unit, Central Public Health Laboratory, London, United Kingdom.

出版信息

J Clin Microbiol. 1994 Aug;32(8):1876-80. doi: 10.1128/jcm.32.8.1876-1880.1994.

Abstract

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.

摘要

1992年在瑞士,由一种此前罕见的血清型——勃兰登堡沙门氏菌引发了一系列持续时间较长的人类沙门氏菌病疫情。为了探究此次疫情的基因型基础,对1983年至1992年间分离出的该血清型代表性菌株进行了分子分型。这些菌株包括1985年之前的散发性人类分离株、来自不同地理区域的分离株,以及1991年之后从瑞士的人类、动物和肉制品中分离出的菌株。研究发现质粒图谱分析不适用于勃兰登堡沙门氏菌,但通过用针对三个标记位点的DNA探针分析限制性片段长度多态性实现了染色体分型;这三个标记位点分别是16S和23S rRNA基因以及移动DNA元件IS200的插入位点。通过脉冲场凝胶电泳检测了全基因组的宏观限制性图谱,结果证明这是分型方法中鉴别力最强的。该研究证明了这些分型方法在流行病学研究中的比较价值和互补关系。所有方法都一致将1992年的分离株鉴定为单一基因型克隆,该克隆存在于多种(食物)感染载体中。它们与该血清型的散发性分离株以及在其他国家分离出的勃兰登堡沙门氏菌菌株不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4812/263895/e06c6313a65c/jcm00008-0056-a.jpg

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