Biofilm Production by Multi Drug Resistant Bacterial Pathogens IsolatedFrom Patients in Intensive Care Units in Egyptian Hospitals

Elhabibi T, R. S
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引用次数: 10

Abstract

Antibiotic resistance among Multi drug resistant (MDR) Gram negative bacteria causing hospital acquired infections poses a great threat in ICU patients. The treatment of such infections has become increasingly problematic, due to their intrinsic and/or acquired resistance to variable classes of antibiotics. Moreover, the demonstrated ability of these bacteria to grow as biofilm is believed to have a major role in their ability to resist various antibiotics. The aim of this study is to evaluate the role of the selected genes in biofilm formation in 3 significant MDR bacterial isolates (Acinetobacter baumannii and Pseudomonas aeruginosa and Stenotrophomonas maltophilia). In this study a total of 625 non replicated Gram negative non-fermenter bacterial isolates were isolated from different clinical specimens from intensive care units from hospitals in Egypt. These bacterial isolates were identified biochemically, API20E and genetically. The antibiogram of all isolates was determined and revealed that all isolates were MDR and colistin was the most potent antibiotic against all A. baumannii and P. aeruginosa isolates. While trimethoprim/sulfamethoxazole combination was the most potent against all S. maltophilia isolates. Detection of biofilm formation of isolates was done by Tube method. While, Quantification of biofilm formation was done by the microtiter plate method using crystal violet (CV) assay. Screening for some selected genes responsible for biofilm formation was done by PCR as bap gene which is responsible for biofilm formation in A. baumannii, rhlI gene in P. aeruginosa strains and rmlA, spgM, rpfF genes in S. maltophilia. The results revealed the presence of these genes in both strong and weak biofilm producer isolates. These final results showed the significance of these genes in biofilm formation.
从埃及医院重症监护病房患者中分离的多重耐药细菌病原体的生物膜生产
多药耐药(MDR)革兰氏阴性菌引起的医院获得性感染对ICU患者的耐药性构成了巨大威胁。由于这些感染对不同种类的抗生素具有内在和/或获得性耐药性,因此治疗这些感染变得越来越成问题。此外,这些细菌作为生物膜生长的能力被认为在它们抵抗各种抗生素的能力中起着重要作用。本研究的目的是评价所选基因在3种重要耐多药菌株(鲍曼不动杆菌、铜绿假单胞菌和嗜麦芽窄养单胞菌)生物膜形成中的作用。在这项研究中,从埃及医院重症监护病房的不同临床标本中共分离出625株非复制革兰氏阴性非发酵细菌。这些细菌分离株经生化、API20E和遗传学鉴定。所有分离株均为耐多药,粘菌素是对鲍曼假单胞菌和铜绿假单胞菌最有效的抗生素。甲氧苄氨嘧啶/磺胺甲恶唑联合用药对嗜麦芽葡萄球菌最有效。采用试管法检测分离菌株的生物膜形成情况。采用结晶紫(CV)微滴板法测定生物膜的形成。采用PCR方法筛选了部分与生物膜形成有关的基因,如鲍曼假单胞菌中与生物膜形成有关的bap基因、铜绿假单胞菌中与生物膜形成有关的rhlI基因和嗜麦芽假单胞菌中与生物膜形成有关的rmlA、spgM、rpfF基因。结果显示,这些基因存在于强和弱生物膜产生菌分离株中。这些最终结果显示了这些基因在生物膜形成中的重要意义。
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