Department of Microbiology, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Department of Microbiology, Faculty of Medicine, Kermanshah University of Medical Sciences, kermanshah, Iran.
BMC Microbiol. 2020 Apr 25;20(1):101. doi: 10.1186/s12866-020-01792-w.
Multi-drug resistant (MDR) Acinetobacter baumannii is one of the most important causes of nosocomial infections. The purpose of this study was to identify antibiotic resistance patterns, biofilm formation and the clonal relationship of clinical and environmental isolates of A. baumannii by Pulsed Field Gel Electrophoresis method. Forty-three clinical and 26 environmental isolates of the MDR A. baumannii were collected and recognized via API 20NE. Antibiotic resistance of the isolates was assessed by the disk diffusion method, and the biofilm formation test was done by the microtiter plate method. Pulsed Field Gel Electrophoresis (PFGE) was used to assess the genomic features of the bacterial isolates.
The resistance rate of clinical and environmental isolates against antibiotics were from 95 to 100%. The difference in antibiotic resistance rates between clinical and environmental isolates was not statistically significant (p > 0.05). Biofilm production capabilities revealed that 31 (44.9%), and 30 (43.5%) isolates had strong and moderate biofilm producer activity, respectively. PFGE typing exhibited eight different clusters (A, B, C, D, E, F, G, and H) with two significant clusters included A and G with 21 (30.4%) and 16 (23.2%) members respectively, which comprises up to 53.6% of all isolates. There was no relationship between biofilm formation and antibiotic resistance patterns with PFGE pulsotypes.
The results show that there is a close relationship between environmental and clinical isolates of A. baumannii. Cross-contamination is also very important that occurs through daily clinical activities between environmental and clinical isolates. Therefore, in order to reduce the clonal contamination of MDR A. baumannii environmental and clinical isolates, it is necessary to use strict infection control strategies.
多重耐药(MDR)鲍曼不动杆菌是医院感染的最重要原因之一。本研究的目的是通过脉冲场凝胶电泳(PFGE)方法鉴定临床和环境分离株的抗生素耐药模式、生物膜形成和克隆关系。收集了 43 株临床和 26 株环境 MDR 鲍曼不动杆菌分离株,并通过 API 20NE 进行鉴定。采用纸片扩散法评估分离株的抗生素耐药性,采用微量滴定板法进行生物膜形成试验。脉冲场凝胶电泳(PFGE)用于评估细菌分离株的基因组特征。
临床和环境分离株对抗生素的耐药率为 95%至 100%。临床和环境分离株的抗生素耐药率差异无统计学意义(p>0.05)。生物膜产生能力显示,31 株(44.9%)和 30 株(43.5%)分离株具有强和中度生物膜产生活性。PFGE 分型显示 8 个不同的聚类(A、B、C、D、E、F、G 和 H),其中 A 和 G 两个显著聚类分别包含 21 株(30.4%)和 16 株(23.2%),占所有分离株的 53.6%。生物膜形成与抗生素耐药模式与 PFGE 脉冲类型之间没有关系。
结果表明,环境和临床鲍曼不动杆菌分离株之间存在密切关系。环境和临床分离株之间的交叉污染也非常重要,这是通过日常临床活动发生的。因此,为了减少 MDR 鲍曼不动杆菌环境和临床分离株的克隆污染,有必要采用严格的感染控制策略。