1 Department of Microbiology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
2 Department of Virology, Pasteur Institute of Iran, Tehran, Iran.
Microb Drug Resist. 2019 May;25(4):558-566. doi: 10.1089/mdr.2018.0146. Epub 2018 Nov 30.
Few studies describe the molecular characterization of mupirocin resistance in strains. In this study, we evaluated the characteristics of mupirocin resistance in isolates for 1-year period in Tehran, Iran. In a cross-sectional study, we collected 51 unique mupirocin-resistant strains obtained from 648 isolates. High- and low-level resistance were determined by minimum inhibitory concentration with broth microdilution method. Presence of the genes for resistance to antibiotics and toxins was detected by polymerase chain reaction assays. Genotyping was performed by protein A () and staphylococcal cassette chromosome mec (SCC) typing, whereas clones were determined by multilocus sequence typing. Among mupirocin-resistant isolates, methicillin-resistant (MRSA) 23 (45.1%) and 28 (54.9%) isolates were classified as high- and low-level mupirocin resistance, respectively. Among the 51 tested strains 25 (49%) isolates were positive for genes. Seven different clones were detected in this study. High-level mupirocin-resistant (HLMUPR) strains belonged to ST8-SCC IV/t064 ( = 10, 19.6%), ST5-SCC IV/t002 ( = 5, 9.8%), ST8-SCC IV/t008 ( = 4, 7.8%), and ST239-SCC III/t631 ( = 4, 7.8%) clones, while low-level mupirocin-resistant (LLMUPR) strains belonged to ST22-SCC IV/t790 ( = 11, 21.6%), ST239-SCC III/t860 ( = 9, 17.7%), and ST15-SCC IV/t084 ( = 8, 15.7%) clones. Two strains belonged to ST22-SCC IV/t790 clone, despite carrying gene, and demonstrated LLMUPR phenotype. One ST8-SCCIV/t008 strain with HLMUPR was confirmed as Vancomycin-intermediate strain. Our data demonstrated the need for thorough epidemiological monitoring and a routine mupirocin testing program to prevent and detect mupirocin resistance in MRSA.
在本研究中,我们评估了伊朗德黑兰为期一年的 分离株中莫匹罗星耐药的特征。在一项横断面研究中,我们收集了 648 株分离株中获得的 51 株独特的莫匹罗星耐药株。采用肉汤微量稀释法测定最低抑菌浓度,确定高、低水平耐药性。采用聚合酶链反应检测抗生素和毒素耐药基因的存在。通过蛋白 A () 和葡萄球菌盒染色体 mec (SCC) 分型进行基因分型,而克隆则通过多位点序列分型确定。在莫匹罗星耐药的分离株中,23 株(45.1%)和 28 株(54.9%)耐甲氧西林的 (MRSA)被分类为高和低水平的莫匹罗星耐药。在 51 株测试菌株中,25 株(49%)菌株的 基因呈阳性。在本研究中检测到 7 种不同的克隆。高水平莫匹罗星耐药(HLMUPR)菌株属于 ST8-SCC IV/t064( = 10,19.6%)、ST5-SCC IV/t002( = 5,9.8%)、ST8-SCC IV/t008( = 4,7.8%)和 ST239-SCC III/t631( = 4,7.8%)克隆,而低水平莫匹罗星耐药(LLMUPR)菌株属于 ST22-SCC IV/t790( = 11,21.6%)、ST239-SCC III/t860( = 9,17.7%)和 ST15-SCC IV/t084( = 8,15.7%)克隆。两株属于 ST22-SCC IV/t790 克隆的菌株携带 基因,但表现出 LLMUPR 表型。一株具有 HLMUPR 的 ST8-SCCIV/t008 菌株被确认为耐万古霉素中间型 株。我们的数据表明,需要进行彻底的流行病学监测和常规莫匹罗星检测计划,以预防和检测耐甲氧西林金黄色葡萄球菌中的莫匹罗星耐药性。