Detection of blaKPC gene among Carbapenem Resistant Enterobacteriacae Isolates from Ain Shams University Hospital, Egypt

Fatma el zahraa Fathy, Maham Anwar
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引用次数: 1

Abstract

Background: Carbapenem resistance among Enterobacteriaceae , especially in Escherichia coli (E.coli) and Klebsiella pneumoniae (K. Pneumoniae) is considered a significant problem worldwide. Resistance to carbapenems in Enterobacteriaceae is mediated by different mechanisms. Production of class-A, Klebsiella pneumoniae carbapenemase (KPC) is the most common mechanisms. Objective: This work aims to measure the frequency of carbapenem resistance among enterobacteriacae isolates and detection of blaKPC gene among them. Methodology: Seventy (70) Enterobacteriaceae isolates were collected from Ain Shams University Hospital during a period of 3 months from February to May 2022.The bacterial isolates were identified by conventional methods. All Enterobacteriaceae isolates were screened for carbapenem resistance by disc diffusion method using meropenem disks. Twenty-five (25) CRE strains were tested for antimicrobial susceptibility testing by the KirbyBauer method. Then E test strips containing range of antibiotic concentrations (0.002-32 ug/ml) for meropenem was done for confirmation of CRE isolates. Twenty-five (25) CRE isolates were subjected to conventional PCR blaKPC gene detection. Results: Out of 70 Enterobacteriaceae isolates 36 strains were identified as K. pneumoniae, 25 were identified as E.coli and 9 were Proteus spp by conventional bacteriological methods. Twenty-five CRE isolates were detected by meropenem disk diffusion method (18 K. pneumoniae and 7 E.coli).. BlaKPC was detected in 3 out of CRE 22 isolates, (13.6%) by conventional PCR. Conclusion: CRE is increasing rapidly worldwide with emergence of BlaKPC gene carbapenem resistance.
埃及艾因沙姆斯大学医院耐碳青霉烯类肠杆菌中blaKPC基因的检测
背景:碳青霉烯耐药在肠杆菌科,特别是大肠杆菌和肺炎克雷伯菌中被认为是一个全球性的重大问题。肠杆菌科细菌对碳青霉烯类的抗性是通过不同的机制介导的。产生a类肺炎克雷伯菌碳青霉烯酶(KPC)是最常见的机制。目的:测定肠杆菌分离株碳青霉烯类耐药频率,并检测其中的blaKPC基因。方法:于2022年2月至5月3个月内从艾因沙姆斯大学医院收集70株肠杆菌科分离株。采用常规方法对分离的细菌进行鉴定。采用美罗培南圆盘扩散法对所有肠杆菌科分离株进行碳青霉烯耐药性筛选。采用KirbyBauer法对25株CRE菌株进行药敏试验。采用抗生素浓度范围(0.002 ~ 32 ug/ml)的美罗培南E试纸条对CRE分离株进行确证。采用常规PCR方法检测25株CRE分离株的blaKPC基因。结果:70株肠杆菌科分离物经常规细菌学方法鉴定为肺炎克雷伯菌36株,大肠杆菌25株,变形杆菌9株。采用美罗培南圆盘扩散法检出25株CRE分离株,其中肺炎克雷伯菌18株,大肠杆菌7株。CRE 22株中有3株检测到BlaKPC,占13.6%。结论:随着BlaKPC基因碳青霉烯类耐药的出现,CRE在全球范围内呈快速上升趋势。
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