Ragheb Suzan Mohammed, Tawfick Mahmoud Mohamed, El-Kholy Amani Ali, Abdulall Abeer Khairy
Department of Microbiology and Immunology, Faculty of Pharmacy, Modern University for Technology and Information (MTI), Cairo 11571, Egypt.
Department of Microbiology and Immunology, Faculty of Pharmacy (Boys), Al-Azhar University, Cairo 11884, Egypt.
Antibiotics (Basel). 2020 Nov 28;9(12):852. doi: 10.3390/antibiotics9120852.
This study aimed at the characterization of carbapenem-resistant isolates focusing on typing of the genes. Additionally, the correlation between the resistance pattern and biofilm formation capacity of the carbapenem-resistant isolates was studied. The collected isolates were assessed for their antimicrobial resistance and carbapenemases production by a modified Hodge test and inhibitor-based tests. The carbapenemases encoding genes (, , , , and ) were detected by PCR. Isolates harboring genes were genotyped by Enterobacterial Repetitive Intergenic Consensus-Polymerase Chain Reaction (ERIC-PCR) and plasmid profile analysis. The discriminatory power of the three typing methods (antibiogram, ERIC-PCR, and plasmid profile analysis) was compared by calculation of Simpson's Diversity Index (SDI). The transferability of gene was tested by chemical transformation. The biofilm formation capacity and the prevalence of the genes encoding the fimbrial adhesins and ) were investigated. The isolates showed remarkable resistance to β-lactams and non-β-lactams antimicrobials. The coexistence of the investigated carbapenemases encoding genes was prevalent except for only 15 isolates. The plasmid profile analysis had the highest discriminatory power (SDI = 0.98) in comparison with ERIC-PCR (SDI = 0.89) and antibiogram (SDI = 0.78). The transferability of gene was unsuccessful. All isolates were biofilm formers with the absence of a significant correlation between the biofilm formation capacity and resistance profile. The genes and were prevalent among the isolates. The prevalence of carbapenemases encoding genes, especially genes in Egyptian healthcare settings, is worrisome and necessitates further strict dissemination control measures.
本研究旨在对耐碳青霉烯类分离株进行特征分析,重点是基因分型。此外,还研究了耐碳青霉烯类分离株的耐药模式与生物膜形成能力之间的相关性。通过改良 Hodge 试验和基于抑制剂的试验,对收集的分离株进行抗菌药物耐药性和碳青霉烯酶产生情况的评估。通过 PCR 检测碳青霉烯酶编码基因(、、、和)。对携带基因的分离株进行肠杆菌重复基因间共识聚合酶链反应(ERIC-PCR)和质粒图谱分析进行基因分型。通过计算辛普森多样性指数(SDI)比较三种分型方法(抗菌谱、ERIC-PCR 和质粒图谱分析)的鉴别力。通过化学转化测试基因的可转移性。研究了生物膜形成能力以及编码菌毛黏附素(和)的基因的流行情况。分离株对β-内酰胺类和非β-内酰胺类抗菌药物表现出显著耐药性。除仅 15 株分离株外,所研究的碳青霉烯酶编码基因共存情况普遍。与 ERIC-PCR(SDI = 0.89)和抗菌谱(SDI = 0.78)相比,质粒图谱分析具有最高的鉴别力(SDI = 0.98)。基因的可转移性未成功。所有分离株均为生物膜形成菌,生物膜形成能力与耐药谱之间无显著相关性。基因和在分离株中普遍存在。在埃及医疗环境中,碳青霉烯酶编码基因的流行情况,尤其是基因,令人担忧,需要进一步采取严格的传播控制措施。