尼日利亚东南部临床样本大肠杆菌和肺炎克雷伯菌中首次发现CIT和DHA AmpC β-内酰胺酶基因

Peace Oluchi Akpu, Henrietta Onyinye Uzoeto, Ikemesit Udeme Peter, Onyinye Lovette Nomeh, Agabus Chidiebube Nwuzo, Rebecca Chinenye Ogba, Ifeanyichukwu Romanus Iroha
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Hence, this study was designed to assess the occurrence of CIT and DHA AmpC β-lactamase gene in Escherichia coli and Klebsiella pnuemoniae from clinical sample in south eastern, Nigeria \nMethodology: This study was conducted over an 8-month period on sixteen (16) non-repetitive clinical isolates of Escherichia coli and Klebsiella pnuemoniae collected from medical microbiology laboratory unit of Alex Ekweume Federal University Teaching Hospital in Abakaliki, Nigeria. The isolates were further identified using Standard microbiological Techniques and screened for cefoxitin resistance using a disc diffusion assay, followed by phenotypic tests using phenyl boronic acid assays for confirmation of AmpC β-lactamases production. 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引用次数: 2

摘要

背景与目的:随着时间的推移,AmpC β-内酰胺酶在肠杆菌尤其是大肠杆菌和肺炎克雷伯菌的抗生素耐药性中发挥着越来越重要的作用。由于产AmpC β-内酰胺酶菌株耐多药表达增加,严重影响了多家医院对患者的护理。因此,本研究旨在评估尼日利亚东南部临床样本中大肠杆菌和肺炎克雷伯菌中CIT和DHA AmpC β-内酰胺酶基因的发生情况。方法:本研究在8个月的时间里,对从尼日利亚阿巴卡利基Alex ekweme联邦大学教学医院医学微生物学实验室收集的16株非重复临床分离的大肠杆菌和肺炎克雷伯菌进行了研究。使用标准微生物学技术进一步鉴定分离株,并使用圆盘扩散试验筛选头孢西丁耐药性,然后使用苯硼酸试验进行表型试验以确认AmpC β-内酰胺酶的产生。采用聚合酶链反应对大肠埃希菌和肺炎克雷伯菌进行AmpC β-内酰胺酶CIT和DHA基因型筛选。结果:16株AmpC β-内酰胺酶产生菌中,男性和女性患者伤口和尿液样本中AmpC β-内酰胺酶基因(DHA和CIT)的检出率均为100%。肺炎克雷伯菌AmpC β-内酰胺酶基因在男性和女性中的总体比例分别为DHA(100%)和CIT(100%)。结论:本研究提示CIT和DHA AmpC基因型的存在。本研究中AmpC β-内酰胺酶的检测具有重要的临床意义,因为这类细菌通常是耐多药的。因此,了解产生AmpC β-内酰胺酶的细菌的存在可能非常有利于获得更准确的流行病学结果并控制其传播,同时需要监测以跟踪任何其他AmpC β-内酰胺酶基因型的进一步传播和出现。
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First Report Occurrence of CIT and DHA AmpC β-lactamase Gene in Escherichia coli and Klebsiella pnuemoniae from Clinical Sample in South Eastern, Nigeria
Background and Objectives: Over time, the enzymes AmpC β-lactamases have become more significant, due to their roles in antibiotic resistance among enterobacteriaceace especially in Escherichia coli and Klebsiella pnuemoniae. Due to increase multidrug resistant express by AmpC β-lactamases producing bacteria strain, the patients care in several hospital has been severely hampered. Hence, this study was designed to assess the occurrence of CIT and DHA AmpC β-lactamase gene in Escherichia coli and Klebsiella pnuemoniae from clinical sample in south eastern, Nigeria Methodology: This study was conducted over an 8-month period on sixteen (16) non-repetitive clinical isolates of Escherichia coli and Klebsiella pnuemoniae collected from medical microbiology laboratory unit of Alex Ekweume Federal University Teaching Hospital in Abakaliki, Nigeria. The isolates were further identified using Standard microbiological Techniques and screened for cefoxitin resistance using a disc diffusion assay, followed by phenotypic tests using phenyl boronic acid assays for confirmation of AmpC β-lactamases production. Escherichia coli and Klebsiella pneumoniae strains were further screen for AmpC β-lactamase CIT and DHA genotype by polymerase chain reactions Result: Of the sixteen (16) confirmed phenotypic AmpC β-lactamase producing bacteria, 100% of the AmpC β-lactamase genes (DHA and CIT) were detected in E. coli from wound and urine samples from both male and female patients. The overall proportion of AmpC β-lactamases gene in Klebsiella pneumoniae were DHA (100 %) and CIT (100 %), in both male and female. Conclusion: This study indicate the occurrence of CIT and DHA AmpC genotype. The detection of AmpC β-lactamases in this study is of clinically importance as such bacteria are often MDR. Thus, being aware of the presence of AmpC β-lactamase-producing bacteria could be very beneficial for achieving more accurate epidemiological results as well as controlling their spread, while surveillance is required to track any further dissemination and emergence of other AmpC β-lactamase genotypes.
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