首页> 美国卫生研究院文献>Journal of Clinical and Diagnostic Research : JCDR >Phenotypic and Genetic Characterization of Carbapenemase and ESBLs Producing Gram-negative Bacteria (GNB) Isolated from Patients with Cystic Fibrosis (CF) in Tehran Hospitals
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Phenotypic and Genetic Characterization of Carbapenemase and ESBLs Producing Gram-negative Bacteria (GNB) Isolated from Patients with Cystic Fibrosis (CF) in Tehran Hospitals

机译:从德黑兰医院囊性纤维化(CF)患者分离的碳青霉烯酶和ESBLs产生革兰氏阴性细菌(GNB)的表型和遗传特征。

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摘要

>Background: Cystic Fibrosis (CF) is an autosomal recessive genetic disorder in white populations caused by mutation in a gene that encodes Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) protein. Since frequent respiratory tract infections are the major problem in patients with CF, obligation to identify the causative bacteria and determining their antibiotic resistance pattern is crucial. The purpose of this project was to detect Gram-negative bacteria (GNB) isolated from sputa of CF patients and to determine their antibiotic resistance pattern.>Materials and Methods: The sputum of 52 CF patients, treated as inpatients at hospitals in Tehran, was obtained between November 2011 and June 2012. Samples cultured in selective and non-selective media and GNB recognized by biochemical tests. Antimicrobial susceptibility testing to cephalosporins, aminoglycosides and carbapenems was performed by disk diffusion method and MICs of them were measured. For phenotypic detection of carbapenemase and ESBLs production, the Modified Hodge test, double disk synergy test and the combined disk methods were performed. Subsequently, the genes encoding the extended spectrum beta-lactamases (blaPER, blaCTX-M) and carbapenemases (blaIMP-1, blaGES, blaKPC, blaNDM, blaVIM-1, blaVIM-2, blaSPM, blaSIM) in Gram negative bacteria were targeted among the resistant isolates by using PCR. PFGE was used to determine any genetic relationship among the Pseudomonas aeruginosa isolated from these patients.>Results: Fifty five GNB were isolated from 52 sputum samples including Pseudomonas aeruginosa, Klebsiella ozaenae, Alcaligenes xylosoxidans, Achromobacter denitrificans, Klebsiella pneumonia and Stenotrophomonas maltophilia. The rates of resistance to different antibiotic were as follows: cefixime (%80), ceftriaxone (%43), ceftazidime (%45) and meropenem (%7). The prevalence of genes encoding the ESBLs and Carbapenemases among the the phenotypically positive strains were as follows: blaCTX-M (19), blaIMP-1 (2), blaVIM-1 (2) and blaVIM-2 (3) genes respectively. No other genes were detected. PFGE analysis revealed 8 genotypes. Six isolates had mutually 3 similar patterns.>Conclusion: This study showed the existence of important ESBLs and carbapenemases genes among the GNB isolated from patients with CF. Continuous surveillance of ESBLs and Carbapenemases, also identification of their types, in bacteria isolated from these patients have an important clinical impact, since, it can often provide valuable information for effective infection control measures and for the choice of appropriate antimicrobial therapy.
机译:>背景:囊性纤维化(CF)是白人人群中的一种常染色体隐性遗传疾病,是由编码囊性纤维化跨膜电导调节剂(CFTR)蛋白的基因突变引起的。由于频繁的呼吸道感染是CF患者的主要问题,因此必须确定致病细菌并确定其抗生素耐药性。该项目的目的是检测从CF患者痰中分离出的革兰氏阴性细菌(GNB)并确定其抗生素耐药性模式。>材料和方法: 52例CF患者的痰液(作为住院患者)该药物于2011年11月至2012年6月在德黑兰的医院获得。在选择性和非选择性培养基中培养的样品以及经生化检验识别的GNB。采用圆盘扩散法对头孢菌素,氨基糖苷类和碳青霉烯类药物进行药敏试验,并测定其MIC。对于表型检测碳青霉烯酶和ESBLs的生产,进行了改良Hodge试验,双盘协同试验和组合盘方法。随后,在革兰氏阴性细菌中靶向了编码超广谱β-内酰胺酶(blaPER,blaCTX-M)和碳青霉烯酶(blaIMP-1,blaGES,blaKPC,blaNDM,blaVIM-1,blaVIM-2,blaSPM,blaSIM)的基因通过PCR鉴定抗性菌株。 >结果:从52个痰液中分离出55个GNB,包括铜绿假单胞菌,产氧克雷伯氏菌,木霉产碱杆菌,氧化亚硝化杆菌,克雷伯氏菌,克雷伯氏菌和嗜麦芽窄食单胞菌。对不同抗生素的耐药率如下:头孢克肟(%80),头孢曲松(%43),头孢他啶(%45)和美罗培南(%7)。在表型阳性菌株中编码ESBLs和碳青霉烯酶的基因的流行程度分别为:blaCTX-M(19),blaIMP-1(2),blaVIM-1(2)和blaVIM-2(3)基因。没有检测到其他基因。 PFGE分析揭示了8个基因型。六个分离株具有彼此相似的3个模式。>结论:该研究表明,从CF患者中分离出的GNB中存在重要的ESBLs和碳青霉烯酶基因。从这些患者中分离出的细菌中,对ESBLs和碳青霉烯酶的连续监测以及鉴定其类型具有重要的临床影响,因为它通常可以为有效的感染控制措施和选择适当的抗菌疗法提供有价值的信息。

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