Genetic profiling of extended-spectrum β-Lactamase and carbapenemase-producing Escherichia coli O157:H7 from clinical samples among diarrheal patients in Shashemene, Ethiopia.

IF 3.4 3区 医学 Q2 INFECTIOUS DISEASES
Shimelis Teshome Ayalneh, Biruk Yeshitela Beshah, Yeonji Jeon, Ashenafi Alemu Wami, Seifegebriel Teshome, Solomon Gebreselassie, Se Eun Park, Mekonnen Teferi, Woldaregay Erku Abegaz
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引用次数: 0

Abstract

Background: Escherichia coli (E. coli) O157:H7, associated with diarrhea, poses a global health risk. In Ethiopia, where diarrhea is common, there is limited knowledge about these resistant strains and a lack of data on Extended-Spectrum β-Lactamase (ESBL) and carbapenemase production. Understanding the prevalence of antimicrobial resistance genes associated with ESBL and carbapenems is crucial for addressing diarrheal disease. This study aimed to investigate the genetic profile of ESBL and carbapenemase coding gene carriage in E. coli O157:H7 from clinical stool samples and evaluate antimicrobial susceptibility patterns.

Methods: A total of twenty-nine bacterial isolates obtained from diarrheal patients were subjected to conventional culture and phenotypic (Kirby Bauer disc diffusion method) testing for antimicrobial resistance. Additionally, screening for the production of ESBL (combined disk method) and carbapenemase (modified carbapenem inactivation method) was conducted. Isolates that tested positive for ESBL and carbapenemase production were further analyzed, targeting five genes (blaNDM, blaKPC, blaCTX-M, blaTEM, and blaSHV) associated with ESBL and carbapenemase production. Data analysis was performed using SPSS version 27.0, employing logistic regression and descriptive statistics.

Results: We analyzed a total of 27 isolates that were ESBL-positive and 12 isolates that were found to produce carbapenemase phenotypically. These isolates were obtained from clinical stool samples and (9/27) 33.3% of the isolates were from under five years children, predominantly from urban areas, and those that have contact with domestic animals. Genes coding ESBL were found in (19/27) 70.4% of the isolates, the most predominant being blaCTX-M and blaTEM. Eight isolates carried blaKPC, but none had blaNDM, while five isolates carried both blaCTX-M and blaTEM genes. blaSHV-carrying isolates showed phenotypic resistance to ampicillin and cephalosporins, while blaKPC-carrying isolates exhibited resistance to ampicillin, carbapenems, and tetracycline.

Conclusion: This study identifies a significant prevalence of multidrug resistance in E. coli O157:H7, which can be attributed to the presence of resistance genes coding for ESBL and carbapenem production. Key factors contributing to this resistance, such as urban environments, children under the age of five, and domestic animal ownership, have been emphasized. Additionally, this research underscores the urgent need for enhanced surveillance and targeted interventions to address this pressing public health concern.

埃塞俄比亚Shashemene腹泻患者临床样本中产生β-内酰胺酶和碳青霉烯酶的大肠杆菌O157:H7的遗传谱分析
背景:大肠杆菌O157:H7与腹泻相关,构成全球健康风险。在腹泻常见的埃塞俄比亚,人们对这些耐药菌株的了解有限,而且缺乏广谱β-内酰胺酶(ESBL)和碳青霉烯酶生产的数据。了解与ESBL和碳青霉烯类相关的抗菌素耐药基因的流行情况对于解决腹泻疾病至关重要。本研究旨在研究临床粪便样本中大肠杆菌O157:H7的ESBL遗传谱和碳青霉烯酶编码基因的携带情况,并评估其抗菌药敏模式。方法:对从腹泻患者中分离的29株细菌进行常规培养和表型(Kirby Bauer圆盘扩散法)耐药试验。筛选ESBL(联合圆盘法)和碳青霉烯酶(改良碳青霉烯酶失活法)的产量。进一步分析ESBL和碳青霉烯酶产生阳性的分离株,针对与ESBL和碳青霉烯酶产生相关的5个基因(blaNDM、blaKPC、blaCTX-M、blaTEM和blaSHV)进行分析。数据分析采用SPSS 27.0版本,采用logistic回归和描述性统计。结果:我们共分析了27株esbl阳性的分离株和12株表型上产生碳青霉烯酶的分离株。这些分离株来自临床粪便样本,(9/27)33.3%的分离株来自5岁以下儿童,主要来自城市地区和与家畜有接触的儿童。在(19/27)70.4%的分离株中检出编码ESBL的基因,其中以blaCTX-M和blaTEM基因居多。8株分离株携带blaKPC基因,未携带blaNDM基因,5株分离株同时携带blaCTX-M和blaNDM基因。携带blashv的分离株对氨苄西林和头孢菌素表现出表型抗性,而携带blakpc的分离株对氨苄西林、碳青霉烯类和四环素表现出耐药性。结论:本研究确定了大肠杆菌O157:H7多药耐药的显著流行,这可能是由于存在编码ESBL和碳青霉烯产生的耐药基因。人们强调了造成这种抗药性的关键因素,如城市环境、五岁以下儿童和家畜所有权。此外,这项研究强调迫切需要加强监测和有针对性的干预措施,以解决这一紧迫的公共卫生问题。
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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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