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首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >Class 1 and class 2 integrons in non-prevalent serovars of Salmonella enterica: structure and association with transposons and plasmids.
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Class 1 and class 2 integrons in non-prevalent serovars of Salmonella enterica: structure and association with transposons and plasmids.

机译:非流行性肠炎沙门氏菌血清中的1类和2类整合子:结构以及与转座子和质粒的结合。

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摘要

OBJECTIVES: To characterize class 1 and class 2 integrons which were simultaneously detected in non-typhoid Salmonella enterica strains of non-prevalent serovars, and to investigate their possible association with transposons and/or plasmids. METHODS: Eight multidrug-resistant S. enterica strains belonging to serovars Virchow (4), Panama (2), Grumpensis (1) and Worthington (1), each containing a class 1 and a class 2 integron, were analysed. Nested PCR amplification was used to determine the gene-cassette configuration of the integrons. Overlapping PCR amplifications were applied in integron-transposon linkage experiments. Conjugation and hybridization experiments were used to localize integrons and transposons in the bacterial genome (plasmid and chromosome associated). RESULTS: One of two different class 1 integrons (with variable regions of 1000 bp/aadA1 and 2300 bp/sat-smr-aadA1) inserted into Tn21-like transposons, were found to coexist with the class 2 integron (2300 bp/dfrA1-sat1-aadA1) of Tn7 in the analysed strains. Class 1 integrons were always found in large conjugative plasmids whereas apparently intact or defective copies of the Tn7 integron could be located on the same plasmid and/or the bacterial chromosome. CONCLUSIONS: This report describes different associations between mobile genetic elements that play a crucial role in the capture and spread of antimicrobial drug resistance. As far as we are aware, this is the first description of class 2 integrons in serovars Panama, Grumpensis and Worthington.
机译:目的:鉴定在非流行型血清型的非伤寒沙门氏菌菌株中同时检测到的1类和2类整合子,并研究它们与转座子和/或质粒的可能关联。方法:分析了8种耐多药性肠炎链球菌,分别属于Virchow(4),Panama(2),Grumpensis(1)和Worthington(1)的血清型,每个菌株均包含1级和2级整合子。巢式PCR扩增用于确定整合子的基因盒结构。重叠PCR扩增应用于整合子-转座子连锁实验。共轭和杂交实验用于定位细菌基因组(质粒和染色体相关)中的整合子和转座子。结果:发现插入Tn21样转座子的两个不同的1类整联蛋白之一(可变区为1000 bp / aadA1和2300 bp / sat-smr-aadA1可变区)与2类整联体(2300 bp / dfrA1-分析菌株中Tn7的sat1-aadA1)。 1型整合素总是在大的结合质粒中发现,而Tn7整合子的完整或有缺陷的拷贝可能位于同一质粒和/或细菌染色体上。结论:本报告描述了在捕获和传播抗微生物药物耐药性中起关键作用的流动遗传元件之间的不同关联。据我们所知,这是对血清型巴拿马,Grumpensis和沃辛顿中2类整合素的首次描述。

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