首页> 外文期刊>Jundishapur Journal of Natural Pharmaceutical Products >The Mutations of Topoisomerase Genes and Their Effect on Resistance to Fluoroquinolones in Extended-Spectrum ?2-Lactamase-Producing Escherichia coli
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The Mutations of Topoisomerase Genes and Their Effect on Resistance to Fluoroquinolones in Extended-Spectrum ?2-Lactamase-Producing Escherichia coli

机译:产广谱β2-内酰胺酶的大肠杆菌中拓扑异构酶基因的突变及其对氟喹诺酮类药物的耐药性

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Background: Fluoroquinolones have been used for empirical treatment of urinary tract infections in recent years. This study aimed at identifying mutations in gyrA and parC genes and their correlation with fluoroquinolone minimal inhibitory concentration (MIC) among extended-spectrum ?2-lactamase-producing (ESBL) Escherichia coli. Methods: A total of 240 E. coli were isolated from urine of patients during 2014 and 2015 in the west of Iran. The isolates were screened for ESBL-producing phenotype using combined disc diffusion test. The susceptibility of ESBL isolates to ciprofloxacin and levofloxacin was determined by disk diffusion and microdilution assay. PCR, sequencing and bioinformatics analysis were performed to identify mutations in gyrA and parC genes. Results: Of 240 isolates, 66 (27.5%) were ESBL positive. Of them, 45 (68.1%) isolates were resistant to both ciprofloxacin and levofloxacin. Sequence analysis showed mutations in the quinolone resistance determining region (QRDR) in the 2 codons (Ser-83, Asp-87) of gyrA and 2 codons (Ser-80, Glu-84) of parC. One mutation at codon of Ala-192 was found outside the QRDR in parC. Conclusions: Isolates with mutations in QRDR of parC and gyrA had the higher MIC level compared to isolates with mutations only in gyrA. The highest level of resistance was detected in isolates with accumulation of mutations in gyrA and parC. A high frequency of fluoroquinolone resistance among ESBL producing E. coli isolates indicated the clustered transmission of resistance genes in this bacterium. A new mutation outside the QRDR of parC was detected, which may play a role in fluoroquinolone resistance.
机译:背景:氟喹诺酮类药物近年来已被用于经验性治疗尿路感染。这项研究的目的是确定广谱β2-内酰胺酶生产(ESBL)大肠杆菌中gyrA和parC基因的突变及其与氟喹诺酮最小抑菌浓度(MIC)的相关性。方法:2014年至2015年期间,在伊朗西部从患者尿液中分离出总共240株大肠杆菌。使用组合圆盘扩散试验筛选分离株的ESBL产生表型。 ESBL分离株对环丙沙星和左氧氟沙星的敏感性通过磁盘扩散和微量稀释测定法测定。进行PCR,测序和生物信息学分析以鉴定gyrA和parC基因中的突变。结果:在240株分离株中,有66株(27.5%)为ESBL阳性。其中,有45(68.1%)个分离株对环丙沙星和左氧氟沙星均具有抗药性。序列分析显示,在parC的2个密码子(Ser-83,Asp-87)和2个密码子(Ser-80,Glu-84)中,喹诺酮抗性确定区(QRDR)发生突变。在parC中的QRDR外部发现了Ala-192密码子的一个突变。结论:与仅在gyrA中具有突变的分离株相比,在parC和gyrA中具有QRDR突变的分离株具有更高的MIC水平。在带有gyrA和parC突变积累的分离株中检测到最高水平的抗性。产生ESBL的大肠杆菌分离株中氟喹诺酮耐药的高频率表明该细菌中耐药基因的簇集传播。检测到parC的QRDR以外的新突变,这可能在氟喹诺酮耐药性中起作用。

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