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Incidence of β-lactamases Among Novel Multidrug Resistant Clinical Isolates of UTI Patients: An Antimicrobial Resistance Surveillance Study

机译:新型UTI患者多药耐药临床分离株中β-内酰胺酶的发生率:一项耐药性监测研究

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Community or Nosocomial Urinary Tract Infections (UTI) are increasing worldwide speedily by creating problem to currently available β-lactam antibiotic therapies. Thus it is an urgent need of research to find the effective therapeutic options to treat / manage the UTI. Therefore, the present work is designed to determine prevalence of β-lactam resistance in seven novel bacterial isolates from the community UTI as well as to identify and characterize the types of β-lactamases involved in UTI. Total Five Hundred and Forty Nine (n= 549) clinical strains isolated from Urine samples and identified as E. coli, P. mirabilis, K. pneumoniae, P. aeruginosa, Enterobacter spp., Escherichia spp., Enterococcus spp., A. haemolyticus, Micrococcus, Serratia spp., Shigella spp., Staph. Aureus etc. Antimicrobial susceptibility profile of these strains revealed high level resistance to Ampicillin (99%), Ceftazidime (98.99%), Amoxicillin (98%), Cefotaxime (99%), Cefaclor (98%) and Penicillin (99%). Thus out of 549 only seven were detected as novel Extended Spectrum β-lactamase producers. All the seven isolates were identified at 16 S r RNA level and submitted to NCBI with following accession numbers such as: JX827388.1, JX827385, JX827384.1, JX827383.1, JX827382, JX827386 and JX827387. Minimum inhibitory concentration of each novel strain was determined against 25 different β-lactam antibiotics i.e. Ampicillin, Amoxiclav, Oxacillin, Vancomycin, Gentamycin, Ciprofloxacin, Nitrofurantoin, Ceftazidime, Cotrimaxazole, Trimethoprim, Imipenam, Amikacin, Amoxicillin, Cephalexin, Cefuroxime, Nalidixic acid, Cefazoline, Cefdinir, Cefexime, Ceftriaxone, Cefuroxime, Cefotaxime, Aztreonam, Cefaclor, Penicillin etc. All these strains revealed to possess virulence markers such as α-hemolysin, Cell surface hydrophobicity, Aerobactin production, Serum Resisitance, Colicine production etc. In addition to this an antimicrobial surveillance of the same strain was tested for multiple antibiotic resistance scale with the help of WHONET software designed by World Health Organization.
机译:社区或医院泌尿道感染(UTI)在世界范围内迅速增加,这是对目前可用的β-内酰胺类抗生素治疗产生了问题。因此,迫切需要进行研究以找到有效的治疗方法来治疗/管理泌尿道感染。因此,本工作旨在确定来自社区UTI的七种新型细菌分离株中β-内酰胺酶的耐药性,以及鉴定和表征涉及UTI的β-内酰胺酶的类型。从尿液样本中分离出总共五百四十九(n = 549)种临床菌株,它们被鉴定为大肠杆菌,奇异杆菌,肺炎克雷伯氏菌,铜绿假单胞菌,肠杆菌属,大肠埃希氏菌,肠球菌属。溶血性,微球菌,沙雷氏菌,志贺氏菌,葡萄球菌。这些菌株的抗菌药敏性显示对氨苄西林(99%),头孢他啶(98.99%),阿莫西林(98%),头孢噻肟(99%),头孢克洛(98%)和青霉素(99%)有高水平的耐药性。因此,在549个样本中,只有7个被检测为新型延伸谱β-内酰胺酶生产者。所有七个分离株均在16 S r RNA水平鉴定,并以下列登录号提交给NCBI:JX827388.1,JX827385,JX827384.1,JX827383.1,JX827382,JX827386和JX827387。确定每种新菌株对25种不同的β-内酰胺抗生素的最小抑菌浓度,这些抗生素分别是氨苄青霉素,阿莫西拉夫,奥沙西林,万古霉素,庆大霉素,环丙沙星,硝基呋喃妥因,头孢他啶,复方新诺明,甲氧苄啶,Imipenam,阿米卡星,阿莫西林,头孢氨苄,头孢呋啶头孢唑啉,头孢地尼,头孢氨苄,头孢曲松,头孢呋辛,头孢噻肟,氨曲南,头孢克洛,青霉素等。所有这些菌株均显示具有毒力标记,例如α-溶血素,细胞表面疏水性,气杆菌素产生,血清抗性,可丽宁产生等。借助世界卫生组织设计的WHONET软件,对同一菌株进行了抗菌监测,测试了多种抗生素耐药性。

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