Department of Microbiology and Immunology, College of Medicine, Kaohsiung Medical University, Taiwan.
Division of Infectious Diseases, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
J Antimicrob Chemother. 2021 Jun 18;76(7):1689-1697. doi: 10.1093/jac/dkab071.
To explore the mechanisms mediating the different levels of gentamicin resistance in enterococci.
Susceptibility testing with gentamicin and PCR of resistance determinants were performed in 149 enterococcal isolates. Genetic relatedness was characterized by MLST and PFGE analysis. Sequences of the aac(6')-Ie-aph(2'')-Ia gene and its surrounding environment were determined by Illumina sequencing. Stability assays of gentamicin resistance were carried out to evaluate the probability of loss of the high-level gentamicin resistance (HLGR) phenotype.
A total of 17 (11.4%) aac(6')-Ie-aph(2'')-Ia-positive enterococcal isolates (2 Enterococcus faecalis and 15 Enterococcus faecium) with non-HLGR phenotype were found. MLST analysis revealed that the 2 E. faecalis belonged to ST116 and ST618, while all the 15 E. faecium belonged to clonal complex 17. Sequence analysis demonstrated that IS1216V was inserted into the 5'-end of aac(6')-Ie-aph(2'')-Ia, leading to loss of HLGR phenotype. Three IS1216V insertion types were found, and type II and III were frequently found in E. faecium. Interestingly, a total of 38 aac(6')-Ie-aph(2'')-Ia-positive E. faecium with HLGR phenotype also had type II or type III IS1216V insertion. Sequencing of the aac(6')-Ie-aph(2'')-Ia-positive HLGR E. faecium E37 revealed that an intact aac(6')-Ie-aph(2'')-Ia was located adjacent to IS1216V-disrupted aac(6')-Ie-aph(2'')-Ia. In a non-antibiotic environment, E37 tended to lose HLGR phenotype with a probability of 1.57 × 10-4, which was largely attributed to homologous recombination between the intact and disrupted aac(6')-Ie-aph(2'')-Ia.
This is first study to elucidate that the E. faecium is capable of changing its HLGR phenotype, which may contribute to adaptation to hospital environments with decreased usage of gentamicin.
探讨肠球菌中不同水平庆大霉素耐药的机制。
对 149 株肠球菌分离株进行庆大霉素药敏试验和耐药决定因子 PCR 检测。采用 MLST 和 PFGE 分析进行遗传相关性分析。通过 Illumina 测序确定 aac(6')-Ie-aph(2'')-Ia 基因及其周围环境的序列。进行庆大霉素耐药稳定性检测,以评估高水平庆大霉素耐药(HLGR)表型丧失的概率。
共发现 17 株(11.4%)具有非 HLGR 表型的 aac(6')-Ie-aph(2'')-Ia 阳性肠球菌分离株(2 株屎肠球菌和 15 株粪肠球菌)。MLST 分析显示,2 株屎肠球菌分别属于 ST116 和 ST618,而 15 株粪肠球菌均属于 17 号克隆复合体。序列分析表明,IS1216V 插入到 aac(6')-Ie-aph(2'')-Ia 的 5'-端,导致 HLGR 表型丧失。发现 3 种 IS1216V 插入类型,II 型和 III 型在粪肠球菌中较为常见。有趣的是,共 38 株具有 HLGR 表型的 aac(6')-Ie-aph(2'')-Ia 阳性粪肠球菌也存在 II 型或 III 型 IS1216V 插入。对 HLGR 粪肠球菌 E37 的 aac(6')-Ie-aph(2'')-Ia 阳性序列分析表明,完整的 aac(6')-Ie-aph(2'')-Ia 位于 IS1216V 破坏的 aac(6')-Ie-aph(2'')-Ia 旁边。在非抗生素环境中,E37 失去 HLGR 表型的概率为 1.57×10-4,这主要归因于完整和破坏的 aac(6')-Ie-aph(2'')-Ia 之间的同源重组。
这是首次阐明粪肠球菌能够改变其 HLGR 表型的研究,这可能有助于其适应庆大霉素使用减少的医院环境。