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对拟杆菌菌株中导致甲硝唑耐药性的遗传元件进行分子研究。

Molecular investigation of genetic elements contributing to metronidazole resistance in Bacteroides strains.

作者信息

Sóki József, Gal Micaela, Brazier Jon S, Rotimi Vincent O, Urbán Edit, Nagy Elisabeth, Duerden Brian I

机构信息

Instutute of Clinical Microbiology, University of Szeged, H-6725 Szeged, Somogyi Béla tér 1, Hungary.

出版信息

J Antimicrob Chemother. 2006 Feb;57(2):212-20. doi: 10.1093/jac/dki443. Epub 2005 Dec 7.

Abstract

OBJECTIVES

The aim of this study was to investigate the constitution of nim gene types, their activating insertion sequence (IS) element, their localization (plasmid or chromosome) and cfiA gene status in metronidazole-resistant Bacteroides strains (n=26) in order to examine their interchangeability.

METHODS

Southern hybridization and conjugative plasmid transfer were used to localize the nimA-E genes and plasmid functions. PCR was used to detect the IS elements and the cfiA genes. PCR-mapping was applied to detect the nim gene-associated IS elements. PCR-mapping products and a nimE gene-containing plasmid fragment were sequenced.

RESULTS

Nine of the nimA genes (12) were activated by IS1168 and nine were carried on plasmids, four of which were pIP417-like. The five nimB genes were chromosomal, and two of them were associated with IS1168 and one with IS612. Of the three nimC genes, two were activated by IS1170, and one was carried on a pIP419-like plasmid. The only nimD gene was chromosomal. The five nimE strains harboured the resistance genes on plasmids: one plasmid, pBF388c, 8.3 kb, was characterized, and a novel IS-like element was demonstrated upstream of all the nimE genes. The insertion events of some of these IS elements were restricted to certain nim gene-specific positions. The 11 chromosomal nim genes displayed a positive association with the cfiA gene-specific background.

CONCLUSIONS

Fourteen strains harboured the well-known genetic elements: pIP417- and pIP419-like plasmids, chromosomal nimB genes and a common nimE plasmid. However, a rate of interchangeability was also demonstrated, mostly due to combinations of nim genes and their associated IS elements harboured on different replicons.

摘要

目的

本研究旨在调查甲硝唑耐药拟杆菌菌株(n = 26)中nim基因类型的构成、其激活插入序列(IS)元件、其定位(质粒或染色体)以及cfiA基因状态,以检验它们的互换性。

方法

采用Southern杂交和接合性质粒转移来定位nimA - E基因和质粒功能。采用聚合酶链反应(PCR)检测IS元件和cfiA基因。应用PCR定位法检测与nim基因相关的IS元件。对PCR定位产物和含nimE基因的质粒片段进行测序。

结果

12个nimA基因中的9个被IS1168激活,9个位于质粒上,其中4个类似pIP417。5个nimB基因位于染色体上,其中2个与IS1168相关,1个与IS612相关。3个nimC基因中,2个被IS1170激活,1个位于类似pIP419的质粒上。唯一的nimD基因位于染色体上。5个nimE菌株在质粒上携带耐药基因:鉴定出一个8.3 kb的质粒pBF388c,并在所有nimE基因上游证实存在一个新的类似IS的元件。其中一些IS元件的插入事件仅限于某些nim基因特异性位置。11个染色体nim基因与cfiA基因特异性背景呈正相关。

结论

14个菌株含有众所周知的遗传元件:类似pIP417和pIP419的质粒、染色体nimB基因和一个常见的nimE质粒。然而,也显示出一定的互换率,主要是由于不同复制子上携带的nim基因及其相关IS元件的组合。

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