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首页> 外文期刊>Journal of infection and public health. >Genomic and antimicrobial resistance genes diversity in multidrug-resistant CTX-M-positive isolates of Escherichia coli at a health care facility in Jeddah
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Genomic and antimicrobial resistance genes diversity in multidrug-resistant CTX-M-positive isolates of Escherichia coli at a health care facility in Jeddah

机译:吉达医疗保健设施在医疗保健设施中大肠杆菌的多药CTX-M阳性分离株的基因组和抗菌性抗菌基因多样性

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Background Whole genome sequencing has revolutionized epidemiological investigations of multidrug-resistant pathogenic bacteria worldwide. Aim of this study was to perform comprehensive characterization of ESBL-positive isolates of Escherichia coli obtained from clinical samples at the King Abdulaziz University Hospital utilizing whole genome sequencing. Methods Isolates were identified by MALDI-TOF mass spectrometry. Genome sequencing was performed using a paired-end strategy on the MiSeq platform. Results Nineteen isolates were clustered into different clades in a phylogenetic tree based on single nucleotide polymorphisms in core genomes. Seventeen sequence types were identified in the extended-spectrum β-lactamase (ESBL)-positive isolates, and 11 subtypes were identified based on distinct types of fim H alleles. Forty-one acquired resistance genes were found in the 19 genomes. The bla subCTX-M-15/sub gene, which encodes ESBL, was found in 15 isolates and was the most predominant resistance gene. Other antimicrobial resistance genes (ARGs) found in the isolates were associated with resistance to tetracycline ( tet A), aminoglycoside [ aph (3″)-Ib, and aph (6)-Id], and sulfonamide ( sul 1, and sul 2). Nonsynonymous chromosomal mutations in the housekeeping genes par C and gyr A were commonly found in several genomes. Conclusion Several other ARGs were found in CTX-M-positive E. coli isolates confer resistance to clinically important antibiotics used to treat infections caused by Gram-negative bacteria.
机译:背景技术全基因组测序在全球范围内彻底改变了多药致病致病菌的流行病学研究。本研究的目的是在利用全基因组测序的情况下,对从Abdulaziz大学医院国王临床样本获得的Escherichia Coli的综合表征。方法通过MALDI-TOF质谱法鉴定分离物。基因组测序使用MiSeq平台上的配对终策略进行。结果基于核心基因组中的单核苷酸多态性,将九分离物聚集成不同的植物中的不同曲线。在扩展光谱β-内酰胺酶(ESBL) - 正性分离物中鉴定了十七种序列类型,基于不同类型的FIM H等位物鉴定了11个亚型。在19个基因组中发现了四十一个获得的抗性基因。编码ESBL的BLA CTX-M-15 基因在15分离株中发现,并且是最主要的抗性基因。在分离株中发现的其他抗菌性抗性基因(Args)与对四环素(TET A)的抗性有关,氨基糖苷[APH(3) - IB和APH(6)-ID]和磺酰胺(Sul 1和Sul 2)相关)。在几种基因组中常见于家庭基因C和Gyr A中的非纯染色体突变。结论在CTX-M阳性大肠杆菌中发现了几种其他args赋予临床重要抗生素的促进促进革兰阴性细菌引起的感染。

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