临床分离肠杆菌科多药耐药菌株的拮抗

Farhat Khurshid
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引用次数: 0

摘要

背景:细菌性病原体中抗菌素耐药性水平的上升是世界范围内最重要的公共卫生问题之一。临床重要细菌的抗生素耐药、耐药类型和水平以及病原体间的多药耐药(MDR)极为重要。随着产esbl肠杆菌科(ESBL-E)引起的感染的增加,以及它们对许多其他抗生素类的共同耐药性,碳青霉烯类被认为是对抗这些危及生命的感染的最后和拯救生命的药物。本研究旨在确定多药耐药菌株引起的肠杆菌科感染的频率、疾病负担和治疗挑战,特别是针对广谱β -内酰胺酶产肠杆菌科(ESBL-E)、碳青霉烯耐药肠杆菌科(CRE)和广谱β -内酰胺酶产碳青霉烯耐药肠杆菌科(ESBL-CRE)引起的新发感染。这项横断面研究于2018年1月至2020年12月在伊斯兰堡诊断中心微生物学系进行,为期两年。通过适当的特性测试,包括选择性使用API 20E,从临床样品培养中分离出肠杆菌科。采用最小抑菌浓度法(MIC)对Vitek 2紧密型培养基进行抗菌药敏试验(AST)和ESBL检测。对一种以上碳青霉烯耐药的分离株被鉴定为碳青霉烯耐药肠杆菌科(CRE)。结果:7270份肠杆菌科细菌标本中,ESBL阳性2943份(40.5%),碳青霉烯耐药487份(6.7%)。进一步分析发现247/487为非ESBL-CRE, 240/487为产ESBL-CRE。最大数量的CRE分离株(非ESBL和ESBL CRE)来自尿液标本。ESBL-CRE的优势菌株为克雷伯菌,其次为大肠杆菌和肠杆菌。进入卫生保健机构是主要的风险因素,其次是年龄增长。结论:除了ESBL-E外,碳青霉烯耐药肠杆菌科(CRE),特别是共同产生广谱β -内酰胺酶(ESBL-CRE)的肠杆菌科(其对碳青霉烯类和β -内酰胺类抗生素的耐药机制在同一生物体中同时表达)已成为令人关注的主要病原体。后者似乎在多重耐药肠杆菌科引起的感染的耐药概况中引入了一个新的维度。关键词:耐碳青霉烯肠杆菌科,广谱β -内酰胺酶,产esbl耐碳青霉烯肠杆菌科,大肠杆菌,克雷伯氏菌,多重耐药肠杆菌科
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Challenge of Multidrug-resistant Strains of Enterobacteriaceae Isolated from Clinical Samples
Background: The rising level of antimicrobial resistance among bacterial pathogens is one of the most significant public health problems worldwide. Antibiotic resistance of clinically important bacteria, the types and levels of resistance and multidrug resistance (MDR) among pathogens is extremely important. With the rise of infections caused by ESBL-producing Enterobacteriaceae (ESBL-E) and with their co-resistance to many other antibiotic classes, carbapenems have been considered to be the last and life-saving agents against these life-threatening infections. The current study was carried out to determine the frequency, disease burden and therapeutic challenge of infections caused by multidrug resistant strains of Enterobacteriaceae with particular reference to Extended-Spectrum Beta-lactamase-producing Enterobacteriaceae (ESBL-E), Carbapenem-resistant Enterobacteriaceae (CRE) and the emerging infections caused by Extended-Spectrum Beta-lactamase-producing Carbapenem-resistant Enterobacteriaceae (ESBL-CRE) Methodology: This cross-sectional study was carried out in the Microbiology Department of Islamabad Diagnostic Centre over a period of two years, from January 2018 to December 2020. Enterobacteriaceae isolated on culture from clinical samples were identified using appropriate characterization tests including the selective use of API 20E. Antimicrobial susceptibility testing (AST) and ESBL detection was performed on Vitek 2 compact system by Minimum Inhibitory Concentration (MIC) methodology. Isolates that were resistant to more than one carbapenem were identified as Carbapenem-Resistant Enterobacteriaceae ( CRE). Results: Out of 7270 specimens that yielded the growth of Enterobacteriaceae, 2943 (40.5%) were ESBL positive (ESBL-E) and 487 (6.7%) were carbapenem resistant (CRE). Further analysis of CRE revealed 247/487 as non-ESBL-CRE and 240/487 as ESBL-producing CRE (ESBL-CRE). Maximum number of CRE isolates - both non-ESBL and ESBL CRE - were from urine specimens. Klebsiella species followed by Eschcerichia coli and Enterobacter were the dominant ESBL-CRE isolates. Admission to a health care facility was the major risk factor followed by advancing age. Conclusion: Besides ESBL-E, Carbapenum-resistant Enterobacteriaceae (CRE), particularly those co-producing Extended-Spectrum Beta-lactamase (ESBL-CRE), (wherein resistance mechanisms to both carbapenems as well as to beta-lactam antibiotics are concomitantly expressed in the same organism), have emerged as the major pathogens of concern. The later appears to have introduced a new dimension in the resistance profile of infections caused by multidrug-resistant enterobacteriaceae. Key words: Carbapenem Resistant Enterobacteriaceae, Extended-Spectrum Beta-Lactamase, ESBL-producing Carbapenem-resistant Enterobacteriaceae, Escherichia coli, Klebsiella, Multi-drug Resistant Enterobacteriaceae.  
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