Darabi Narges, Motazakker Morteza, Khalkhali Hamid Reza, Yousefi Saber
Department of Microbiology and Virology, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Cellular and Molecular Research Center, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
J Infect Dev Ctries. 2019 Aug 31;13(8):690-697. doi: 10.3855/jidc.9985.
Klebsiella pneumoniae is an opportunistic pathogen accounting for 5-7% of hospital acquired infections. The emergence of carbapenem-resistant Klebsiella pneumoniae has been increasing rapidly over recent years causing many therapeutic problems worldwide. This study aimed to research the antimicrobial resistance profile, detect β-lactamase genes among clinical isolates of K. pneumoniae, and determine their clonal relatedness.
All Klebsiella pneumoniae isolates were obtained from teaching hospitals in Urmia, Iran. Antimicrobial susceptibility testing was done by the disk diffusion method. Furthermore, minimum inhibitory concentrations of imipenem were determined by applying Etest strips. Screening of β-lactamase-producing isolates was performed by the combined disk method and modified Hodge test. The detection of β-lactamase genes was conducted by polymerase chain reaction (PCR), and isolates' clonal relatedness was evaluated by random amplified polymorphic DNA (RAPD)-PCR.
Overall, 45 out of 182 (24.7%) K. pneumoniae isolates were non-susceptible to imipenem. The combined disk method and modified Hodge test revealed that 93.3% and 71.1% of the imipenem non-susceptible isolates were β-lactamase producers, respectively. The presence of blaVIM, blaNDM, blaKPC, and blaIMP genes was confirmed in 48.9%, 15.6%, 11.1%, and 6.7% of the β-lactamase-producing isolates, respectively. RAPD-PCR revealed that 73% of these isolates were classified into six different clusters.
A relatively high prevalence of β-lactamase genes was seen among multidrug-resistant isolates of K. pneumoniae. Most patients infected with β-lactamase-producing isolates had a history of long-term hospitalization and nosocomial infections. The predominance of β-lactamase genes in intensive care unit and internal units alarm clinicians to the growth of hospitalization and mortality rates.
肺炎克雷伯菌是一种机会致病菌,占医院获得性感染的5%-7%。近年来,耐碳青霉烯类肺炎克雷伯菌的出现迅速增加,在全球范围内引发了许多治疗问题。本研究旨在研究肺炎克雷伯菌临床分离株的抗菌药物耐药谱,检测β-内酰胺酶基因,并确定它们的克隆相关性。
所有肺炎克雷伯菌分离株均取自伊朗乌尔米耶的教学医院。采用纸片扩散法进行抗菌药物敏感性试验。此外,应用Etest试纸条测定亚胺培南的最低抑菌浓度。通过联合纸片法和改良Hodge试验对产β-内酰胺酶的分离株进行筛选。通过聚合酶链反应(PCR)检测β-内酰胺酶基因,并通过随机扩增多态性DNA(RAPD)-PCR评估分离株的克隆相关性。
总体而言,182株肺炎克雷伯菌分离株中有45株(24.7%)对亚胺培南不敏感。联合纸片法和改良Hodge试验显示,分别有93.3%和71.1%的亚胺培南不敏感分离株为β-内酰胺酶产生菌。在产β-内酰胺酶的分离株中,blaVIM、blaNDM、blaKPC和blaIMP基因的存在分别在48.9%、15.6%、11.1%和6.7%的菌株中得到证实。RAPD-PCR显示,这些分离株中有73%被分为六个不同的簇。
在多重耐药的肺炎克雷伯菌分离株中,β-内酰胺酶基因的流行率相对较高。大多数感染产β-内酰胺酶分离株的患者有长期住院和医院感染史。重症监护病房和内科病房中β-内酰胺酶基因的优势提醒临床医生注意住院率和死亡率的上升。