AlQumaizi Khalid I, Kumar Sunil, Anwer Razique, Mustafa Shoeb
Department of Family Medicine, College of Medicine, AlMareefa University, Riyadh 11597, Saudi Arabia.
Department of Medical Microbiology, Post Graduate Institute of Medical Education & Research, Sector-12, Chandigarh 160012, India.
Life (Basel). 2022 Mar 14;12(3):419. doi: 10.3390/life12030419.
Background: Acinetobacter baumannii is an opportunistic pathogen associated with healthcare infections and high mortality rates in intensive care units all over the globe. Porins and efflux pumps over-expression have been reported as contributing factors in escalating drug resistance and rendering treatment ineffective. In this study, we investigated the mechanisms of multidrug resistance (MDR) in A. baumannii clinical isolates. Methods: A total of 30 A. baumannii isolates were included in the present study from Nehru Hospital (PGIMER-Chandigarh) located in North India. Kirby Bauer disk diffusion assay and MIC were performed to determine the antimicrobial susceptibility pattern. Screening of beta-lactamases was performed using PCR. Relative gene expression of four RND, one MATE efflux pump, and two outer membrane proteins were determined using RT-PCR. Molecular typing of 22 isolates was carried out using MLST Oxford scheme. Results: CarO porin genes showed over-expression in 63% isolates followed by adeGandabeM efflux pump downregulation/underexpression (<0.5 fold), suggesting the carbapenem-susceptible phenotypic nature of the isolates. High prevalence of VIM-2, NDM-1, and OXA-23 genes was observed in A. baumannii isolates. Interestingly, NDM-1 and OXA-58 were traced in 10 and3 A. baumannii isolates respectively; 13 of 22 (59%) isolates showed novel Sequence Types (STs) in the Multi-Locus Sequence Typing (MLST) analysis. ST 1087 was most commonly found ST among all others (16 STs). Conclusions: This study indicated a possible role of carO porin genes and adeG (RND) andabeM (MATE) efflux pumps in carbapenem susceptibility of A. baumannii. New STs were also reported in the majority of the isolates.
鲍曼不动杆菌是一种机会致病菌,与全球重症监护病房的医院感染及高死亡率相关。据报道,孔蛋白和外排泵的过度表达是导致耐药性增加及治疗无效的因素。在本研究中,我们调查了鲍曼不动杆菌临床分离株的多重耐药机制。方法:本研究共纳入了来自印度北部尼赫鲁医院(昌迪加尔全印医学科学研究所)的30株鲍曼不动杆菌分离株。采用 Kirby Bauer 纸片扩散法和 MIC 法测定抗菌药物敏感性模式。使用 PCR 法筛选β-内酰胺酶。采用 RT-PCR 法测定四种 RND、一种 MATE 外排泵和两种外膜蛋白的相对基因表达。使用 MLST 牛津方案对22株分离株进行分子分型。结果:CarO 孔蛋白基因在63%的分离株中呈过表达,其次是 adeG 和 abeM 外排泵下调/低表达(<0.5倍),提示分离株对碳青霉烯类药物敏感的表型特征。在鲍曼不动杆菌分离株中观察到 VIM-2、NDM-1 和 OXA-23 基因的高流行率。有趣的是,分别在10株和3株鲍曼不动杆菌分离株中检测到 NDM-1 和 OXA-58;在多位点序列分型(MLST)分析中,22株中有13株(59%)显示出新的序列类型(STs)。ST 1087 是所有其他类型(16种 STs)中最常见的 ST。结论:本研究表明 CarO 孔蛋白基因以及 adeG(RND)和 abeM(MATE)外排泵在鲍曼不动杆菌对碳青霉烯类药物的敏感性中可能起作用。大多数分离株中也报道了新的 STs。