Mazandaran University of Medical Sciences, Faculty of Medicine, Molecular and Cell Biology Research Centre, Sari, Iran.
Mazandaran University of Medical Sciences, Faculty of Medicine, Department of Medical Microbiology and Virology, Sari, Iran.
Rev Soc Bras Med Trop. 2021 Jan 29;54:e05992020. doi: 10.1590/0037-8682-0599-2020. eCollection 2021.
This study aimed to determine the role of genes encoding aminoglycoside-modifying enzymes (AMEs) and 16S rRNA methylase (ArmA) in Acinetobacter baumannii clinical isolates.
We collected 100 clinical isolates of A. baumannii and identified and confirmed them using microbiological tests and assessment of the OXA-51 gene. Antibiotic susceptibility testing was carried out using disk agar diffusion and micro-broth dilution methods. The presence of AME genes and ArmA was detected by PCR and multiplex PCR.
The most and least effective antibiotics in this study were netilmicin and ciprofloxacin with 68% and 100% resistance rates, respectively. According to the minimum inhibitory concentration test, 94% of the isolates were resistant to gentamicin, tobramycin, and streptomycin, while the highest susceptibility (20%) was observed against netilmicin. The proportion of strains harboring the aminoglycoside resistance genes was as follows: APH(3')-VIa (aphA6) (77%), ANT(2")-Ia (aadB) (73%), ANT(3")-Ia (aadA1) (33%), AAC(6')-Ib (aacA4) (33%), ArmA (22%), and AAC(3)-IIa (aacC2) (19%). Among the 22 gene profiles detected in this study, the most prevalent profiles included APH(3')-VIa + ANT(2")-Ia (39 isolates, 100% of which were kanamycin-resistant), and AAC(3)-IIa + AAC(6')-Ib + ANT(3")-Ia + APH(3')-VIa + ANT(2")-Ia (14 isolates, all of which were resistant to gentamicin, kanamycin, and streptomycin).
High minimum inhibitory concentration of aminoglycosides in isolates with the simultaneous presence of AME- and ArmA-encoding genes indicated the importance of these genes in resistance to aminoglycosides. However, control of their spread could be effective in the treatment of infections caused by A. baumannii.
本研究旨在确定氨基糖苷修饰酶(AMEs)和 16S rRNA 甲基化酶(ArmA)基因在鲍曼不动杆菌临床分离株中的作用。
我们收集了 100 株鲍曼不动杆菌临床分离株,通过微生物学试验和 OXA-51 基因评估进行鉴定和确认。采用纸片琼脂扩散法和微量肉汤稀释法进行抗生素药敏试验。通过 PCR 和多重 PCR 检测 AME 基因和 ArmA 的存在。
本研究中最有效和最无效的抗生素分别为奈替米星和环丙沙星,耐药率分别为 68%和 100%。根据最低抑菌浓度试验,94%的分离株对庆大霉素、妥布霉素和链霉素耐药,而对奈替米星的敏感性最高(20%)。携带氨基糖苷类耐药基因的菌株比例如下:APH(3')-VIa(aphA6)(77%)、ANT(2")-Ia(aadB)(73%)、ANT(3")-Ia(aadA1)(33%)、AAC(6')-Ib(aacA4)(33%)、ArmA(22%)和 AAC(3)-IIa(aacC2)(19%)。在本研究中检测到的 22 种基因谱中,最常见的基因谱包括 APH(3')-VIa + ANT(2")-Ia(39 株,全部对卡那霉素耐药)和 AAC(3)-IIa + AAC(6')-Ib + ANT(3")-Ia + APH(3')-VIa + ANT(2")-Ia(14 株,全部对庆大霉素、卡那霉素和链霉素耐药)。
同时存在 AME 和 ArmA 编码基因的分离株对氨基糖苷类药物的最低抑菌浓度较高,表明这些基因在氨基糖苷类药物耐药中具有重要作用。然而,控制这些基因的传播可能对治疗由鲍曼不动杆菌引起的感染有效。