Yadav Kamlesh Kumar, Adhikari Nabaraj, Khadka Rama, Pant Anil Dev, Shah Bibha
Department of Microbiology, Kantipur College of Medical Science, Sitapaila, Kathmandu, Nepal.
Consultant pathologist, National Kidney Center, Vanasthali, Kathmandu, Nepal.
Antimicrob Resist Infect Control. 2015 Oct 26;4:42. doi: 10.1186/s13756-015-0085-0. eCollection 2015.
Emergence of antibacterial resistance and production of Extended spectrum β-lactamases (ESBLs) are responsible for the frequently observed empirical therapy failures. Most countries have experienced rapid dissemination of ESBLs producing Enterobacteriaceae isolates, particularly E. coli and Klebsiella pneumoniae. ESBLs are clinically significant and when detected, indicate the need for the use of appropriate antibacterial agents. But antibacterial choice is often complicated by multi-resistance.
This study was carried from June to November 2014 to study the multidrug resistant (MDR) Enterobacteriaceae and ESBL producing E. coli among urine isolates in hospital setting. Isolates from urine samples were primarily screened for possible ESBL production followed by phenotypic confirmation. Antibiotic susceptibility testing (AST) was done by Kirby Bauer disk diffusion method following Clinical and Laboratory Standard Institute (CLSI) guidelines.
Out of 450 urine samples processed, 141 significant growths were obtained including 95 Enterobacteriaceae isolates with 67 E. coli. Among Enterobacteriaceae, 92 (96.84 %) were recorded as MDR and 18 (26.87 %) E. coli were confirmed as ESBLs producers.
Using the phenotypic confirmatory test forwarded by the CLSI, relatively significant E. coli isolates tested were ESBL producers. Also high numbers of MDR organisms were isolated among Enterobacteriaceae. Isolates showed significant resistance to the commonly prescribed drugs. These findings suggest for further study in this field including the consequences of colonization with MDR and ESBL-producing bacteria both in the community and in the hospital setting.
抗菌药物耐药性的出现以及超广谱β-内酰胺酶(ESBLs)的产生是导致常见经验性治疗失败的原因。大多数国家都经历了产ESBLs的肠杆菌科分离株,尤其是大肠埃希菌和肺炎克雷伯菌的快速传播。ESBLs具有临床意义,一旦检测到,就表明需要使用合适的抗菌药物。但抗菌药物的选择常常因多重耐药性而变得复杂。
本研究于2014年6月至11月开展,旨在研究医院环境中尿液分离株中的多重耐药(MDR)肠杆菌科细菌及产ESBLs的大肠埃希菌。首先对尿液样本分离株进行ESBLs产生可能性的初步筛查,随后进行表型确认。按照临床和实验室标准协会(CLSI)指南,采用 Kirby Bauer纸片扩散法进行抗生素敏感性试验(AST)。
在处理的450份尿液样本中,获得141份有意义的培养物,其中包括95份肠杆菌科分离株,其中67份为大肠埃希菌。在肠杆菌科中,92份(96.84%)被记录为多重耐药,18份(26.87%)大肠埃希菌被确认为ESBLs生产者。
使用CLSI提出的表型确认试验,检测的大肠埃希菌分离株中相对有意义的部分为ESBLs生产者。在肠杆菌科中还分离出大量多重耐药菌。分离株对常用药物表现出显著耐药性。这些发现表明需要在该领域进行进一步研究,包括社区和医院环境中多重耐药菌和产ESBLs细菌定植的后果。