尼日利亚某三级医院尿路感染患者中产生广谱β -内酰胺酶的大肠杆菌编码氨基糖苷和氟喹诺酮耐药基因

IF 3 3区 医学 Q2 INFECTIOUS DISEASES
Micheal Anorue, Chika Ejikeugwu, Chidinma Stacy Iroha, Ebuka Elijah David, Ejike Francis Nwabueze, Ifeanyichukwu Romanus Iroha
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引用次数: 0

摘要

大肠杆菌引起的尿路感染(uti)仍然是门诊和住院患者中最常见的细菌感染。本研究旨在检测UTI患者中含有氨基糖苷类和氟喹诺酮耐药基因的广谱β -内酰胺酶产生大肠杆菌。在尼日利亚阿巴卡利基Alex Ekwueme联邦大学教学医院(AE-FUTHA)共收集了372份尿路感染患者的中游尿液样本。采用标准微生物学和分子方法分离鉴定大肠杆菌。采用双盘协同试验法检测产esbl大肠杆菌。采用标准Kirby-Bauer纸片扩散法对产esbl大肠杆菌进行药敏试验。采用pcr特异性引物筛选ESBL、氨基糖苷类和氟喹诺酮类耐药基因。在收集的372份尿液样本中,检出84株(22.58%)不同的大肠杆菌,其中24株(28.57%)为ESBL阳性。所有菌株对阿莫西林/克拉维酸24耐药(100%),其余菌株对氨曲南和磺胺甲恶唑/甲氧苄啶22耐药(91.7%),头孢曲松21耐药(87.5%),头孢他啶和头孢噻肟16耐药(66.7%)。15例(62.5%)对氟喹诺酮类药物和环丙沙星耐药。在24株esbl阳性分离株中,根据它们对氨基糖苷类和氟喹诺酮类抗生素的耐药性选择了12株。这些产生esbl的大肠杆菌编码blaOXA-1 3(25%)、blaSHV 3(25%)和blaTEM 8(66.7%)。所有分离株中检出氟喹诺酮类基因、qnrA和qnrC 12株(100%),qnrB 10株(83.35)。所有菌株12(100%)检测到氨基糖苷基因ant(4’)-la, 10(83.3%)检测到aph(2’)-ld。8例患者(66.7%)对ESBL、氟喹诺酮和氨基糖苷(blaTEM + qnrA + qnrB + qnrC + ant(4′)-la + aph(2′)-lb)共耐药。大肠杆菌是Abakaliki从尿路感染患者中分离出的主要细菌之一。较高比例的菌株具有产生ESBL的能力,主要编码含有氟喹诺酮类基因qnr和氨基糖苷ant(4′)-la共存的blaTEM。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Extended spectrum beta-lactamase producing Escherichia coli encoding aminoglycoside and fluoroquinolone resistant genes in urinary tract infection patients in a tertiary hospital in Nigeria.

Escherichia coli causing urinary tract infections (UTIs) remains the most common bacterial infection diagnosed among outpatients as well as hospitalized patients. This study aimed to detect the extended-spectrum beta-lactamase-producing E. coli habouring aminoglycosides and fluoroquinolone-resistant genes in UTI patients. A total of 372 clean-catch midstream urine samples of patients with UTI attending Alex Ekwueme Federal University Teaching Hospital Abakaliki, Nigeria (AE-FUTHA) was collected. The collected urine samples were processed using standard microbiology and molecular methods to isolate and identify E. coli. Detection of ESBL-producing E. coli was performed using the double-disk synergy test. The ESBL-producing E. coli were subjected to antimicrobial susceptibility testing following the standard Kirby-Bauer disk diffusion method. PCR-specific primers were used to screen for the ESBL, aminoglycosides and fluoroquinolone-resistant genes. Out of the 372 urine samples collected, 84 (22.58%) distinct E. coli isolates were recovered, out of which 24 (28.57%) were ESBL positive. While all the isolates were resistant to amoxicillin/clavulanic acid 24 (100%), others were highly resistant to aztreonam and sulfamethoxazole/trimethoprim 22 (91.7%), ceftriaxone 21 (87.5%), ceftazidime and cefotaxime 16 (66.7%). Resistance to a fluoroquinolone, a ciprofloxacin was observed in 15 (62.5%). Out of the 24 ESBL-positive isolates, 12 were selected based on their resistance to both aminoglycosides and fluoroquinolones antibiotics used. These ESBL-producing E. coli encoded blaOXA-1 3 (25%), blaSHV 3 (25%) and blaTEM 8 (66.7%). Fluoroquinolone genes, qnrA and qnrC were detected in all the isolates 12 (100%), while qnrB was detected in 10 (83.35). Aminoglycoside gene, ant (4')-la was detected in all the isolates 12 (100%), while aph (2")-ld was haboured by 10 (83.3%). Co-resistance of ESBL, fluoroquinolone and aminoglycoside (blaTEM + qnrA + qnrB + qnrC + ant (4')-la + aph (2")-lb) was observed in 8(66.7%). E. coli is one of the predominant bacteria isolated from UTI patients in Abakaliki. A high proportion have the ability to produce ESBL and predominantly encoded blaTEM with co-existence of fluoroquinolone gene, qnr and aminoglycoside, ant (4')-la.

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来源期刊
BMC Infectious Diseases
BMC Infectious Diseases 医学-传染病学
CiteScore
6.50
自引率
0.00%
发文量
860
审稿时长
3.3 months
期刊介绍: BMC Infectious Diseases is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of infectious and sexually transmitted diseases in humans, as well as related molecular genetics, pathophysiology, and epidemiology.
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