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The occurrence of ESBL-producing Escherichia coli carrying aminoglycoside resistance genes in urinary tract infections in Saudi Arabia

机译:沙特阿拉伯泌尿道感染中携带氨基糖苷抗性基因的产ESBL大肠杆菌的发生

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Background The infection and prevalence of extended-spectrum β-lactamases (ESBLs) is a worldwide problem, and the presence of ESBLs varies between countries. In this study, we investigated the occurrence of plasmid-mediated ESBL/AmpC/carbapenemase/aminoglycoside resistance gene expression in Escherichia coli using phenotypic and genotypic techniques. Methods A total of 58 E. coli isolates were collected from hospitals in the city of Makkah and screened for the production of ESBL/AmpC/carbapenemase/aminoglycoside resistance genes. All samples were subjected to phenotypic and genotypic analyses. The antibiotic susceptibility of the E. coli isolates was determined using the Vitek-2 system and the minimum inhibitory concentration (MIC) assay. Antimicrobial agents tested using the Vitek 2 system and MIC assay included the expanded-spectrum (or third-generation) cephalosporins (e.g., cefoxitin, cefepime, aztreonam, cefotaxime, ceftriaxone, and ceftazidime) and carbapenems (meropenem and imipenem). Reported positive isolates were investigated using genotyping technology (oligonucleotide microarray-based assay and PCR). The genotyping investigation was focused on ESBL variants and the AmpC, carbapenemase and aminoglycoside resistance genes . E . coli was phylogenetically grouped, and the clonality of the isolates was studied using multilocus sequence typing (MLST). Results Our E. coli isolates exhibited different levels of resistance to ESBL drugs, including ampicillin (96.61%), cefoxitin (15.25%), ciprofloxacin (79.66%), cefepime (75.58%), aztreonam (89.83%), cefotaxime (76.27%), ceftazidime (81.36%), meropenem (0%) and imipenem (0%). Furthermore, the distribution of ESBL-producing E. coli was consistent with the data obtained using an oligonucleotide microarray-based assay and PCR genotyping against genes associated with β-lactam resistance. ST131 was the dominant sequence type lineage of the isolates and was the most uropathogenic E. coli lineage. The E. coli isolates also carried aminoglycoside resistance genes. Conclusions The evolution and prevalence of ESBL-producing E. coli may be rapidly accelerating in Saudi Arabia due to the high visitation seasons (especially to the city of Makkah). The health authority in Saudi Arabia should monitor the level of drug resistance in all general hospitals to reduce the increasing trend of microbial drug resistance and the impact on patient therapy.
机译:背景技术广谱β-内酰胺酶(ESBLs)的感染和流行是一个世界性的问题,ESBLs的存在因国家而异。在这项研究中,我们调查了使用表型和基因型技术在质粒中介导的质粒介导的ESBL / AmpC /卡巴内切酶/氨基糖苷抗性基因的表达。方法从麦加市的医院中收集了总共58株大肠杆菌,并筛选出ESBL / AmpC / carbapenemase / aminoglycoside抗性基因的产生。对所有样品进行表型和基因型分析。使用Vitek-2系统和最小抑菌浓度(MIC)测定法确定了大肠杆菌分离株的抗生素敏感性。使用Vitek 2系统和MIC分析测试的抗菌剂包括广谱(或第三代)头孢菌素(例如头孢西丁,头孢吡肟,氨曲南,头孢噻肟,头孢曲松和头孢他啶)和碳青霉烯(美罗培南和亚胺培南)。使用基因分型技术(基于寡核苷酸微阵列的测定和PCR)对报告的阳性分离株进行了研究。基因分型研究的重点是ESBL变体和AmpC,碳青霉烯酶和氨基糖苷抗性基因。 E.对大肠埃希菌进行了系统发育分类,并使用多基因座序列分型(MLST)研究了分离株的克隆性。结果我们的大肠杆菌分离物对ESBL药物表现出不同水平的抗药性,包括氨苄西林(96.61%),头孢西丁(15.25%),环丙沙星(79.66%),头孢吡肟(75.58%),氨曲南(89.83%),头孢噻肟(76.27%) ),头孢他啶(81.36%),美罗培南(0%)和亚胺培南(0%)。此外,产ESBL的大肠杆菌的分布与使用基于寡核苷酸微阵列的测定和针对与β-内酰胺抗性相关的基因的PCR基因分型所获得的数据一致。 ST131是分离株的主要序列类型谱系,并且是最引起尿毒症的大肠杆菌谱系。大肠杆菌分离物还携带氨基糖苷抗性基因。结论在沙特阿拉伯,由于人流旺盛的季节(尤其是到麦加市),其进化和流行可能正在迅速加速。沙特阿拉伯的卫生当局应监测所有综合医院的耐药性水平,以减少微生物耐药性的增长趋势以及对患者治疗的影响。

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