Medical Microbiology Research Center, Qazvin University of Medical Sciences, Qazvin, IR, Iran.
Medical Microbiology Research Center, Qazvin University of Medical Sciences, Qazvin, IR, Iran.
Infect Genet Evol. 2018 Oct;64:219-224. doi: 10.1016/j.meegid.2018.06.030. Epub 2018 Jun 28.
Production of aminoglycoside modifying enzymes (AMEs) and 16S rRNA methylases are two main resistance mechanisms against these antibiotics. This study determined the frequency of AMEs and 16 s rRNA methylase genes among aminoglycoside non-susceptible K. pneumoniae isolates and evaluated their clonal relationship by enterobacterial repetitive intergenic consensus (ERIC)-PCR. A total of 177 K. pneumoniae isolates were collected from hospitals of Qazvin and Tehran, Iran. The identification of isolates was done by standard laboratory methods and API 20E strips. Aminoglycosides susceptibility was determined by Kirby-Bauer method and AMEs and 16S rRNA methylase encoding genes were studied by PCR and sequencing methods. Clonal relatedness of isolates was assessed by ERIC-PCR method. In total, 74% of isolates were non-susceptible to the aminoglycosides used in the study among those kanamycin 110 (62.1%), tobramycin 91 (51.4%), and gentamycin 87 (49.2%) showed the highest rates of resistance whereas netilmicin and amikacin revealed high susceptibility rates of 67.8% and 61.0%, respectively. Of 130 aminoglycoside non-susceptible isolates, 91.5% were positive for the presence of aac(6')-Ib as the most dominant gene followed by aac(3)-II (78.5%), aph(3')-IIIa (14.6%), ant(4')-Ia (3.1%), and armA (7.7%) either alone or in combination. ERIC-PCR results showed 67.7% of non-susceptible isolates had different banding patterns followed by three distinct clones including A (16.2%), B (10.8%), and C (5.4%). Among those isolates carrying AMEs genes, 85 (68%) isolates belonged to independent groups and 21 (16.8%), 12 (9.6%), and 7 (5.6%) isolates belonged to groups A, B, and C, respectively, whereas 7 (70%) of 16S rRNA methylase-producing isolates belonged to independent groups. Our results revealed high prevalence of AMEs with the emergence of armA genes among the genetically unrelated resistant isolates of K. pneumonia in Iran, suggesting the need for more effective therapeutic strategies to reduce the selection pressure and better management of the patients infected with these resistant isolates.
氨基糖苷类修饰酶(AMEs)和 16S rRNA 甲基化酶的产生是这些抗生素产生耐药性的两种主要机制。本研究确定了对氨基糖苷类药物不敏感的肺炎克雷伯菌分离株中 AMEs 和 16S rRNA 甲基化酶基因的频率,并通过肠杆菌重复基因间共识(ERIC)-PCR 评估了它们的克隆关系。从伊朗的 Qazvin 和德黑兰的医院共收集了 177 株肺炎克雷伯菌分离株。通过标准实验室方法和 API 20E 条带对分离株进行鉴定。通过 Kirby-Bauer 法测定氨基糖苷类药物的敏感性,通过 PCR 和测序法研究 AMEs 和 16S rRNA 甲基化酶编码基因。通过 ERIC-PCR 方法评估分离株的克隆相关性。在研究中使用的氨基糖苷类药物中,共有 74%的分离株对这些药物不敏感,其中卡那霉素 110(62.1%)、妥布霉素 91(51.4%)和庆大霉素 87(49.2%)的耐药率最高,而奈替米星和阿米卡星的耐药率分别为 67.8%和 61.0%。在 130 株氨基糖苷类药物不敏感的分离株中,91.5%的分离株存在 aac(6')-Ib 作为最主要的基因,其次是 aac(3)-II(78.5%)、aph(3')-IIIa(14.6%)、ant(4')-Ia(3.1%)和 armA(7.7%),这些基因单独或组合存在。ERIC-PCR 结果显示,67.7%的非敏感分离株具有不同的带型,其次是三个不同的克隆,包括 A(16.2%)、B(10.8%)和 C(5.4%)。在携带 AMEs 基因的分离株中,85(68%)株属于独立组,21(16.8%)、12(9.6%)和 7(5.6%)株分别属于 A、B 和 C 组,而 7(70%)株产生 16S rRNA 甲基化酶的分离株属于独立组。我们的结果表明,在伊朗与遗传无关的耐多药肺炎克雷伯菌分离株中,AMEs 的流行率很高,同时出现了 armA 基因,这表明需要更有效的治疗策略来降低选择压力,并更好地管理感染这些耐药分离株的患者。