Senok Abiola, Somily Ali M, Nassar Rania, Garaween Ghada, Kim Sing Garwin, Müller Elke, Reissig Annett, Gawlik Darius, Ehricht Ralf, Monecke Stefan
Department of Basic Medical Sciences, College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates.
Department of Pathology and Laboratory Medicine, College of Medicine, King Khalid University Hospital and King Saud University, Riyadh, Saudi Arabia.
Infect Drug Resist. 2019 Sep 3;12:2739-2746. doi: 10.2147/IDR.S218870. eCollection 2019.
There is a need for continuous surveillance of methicillin-resistant (MRSA) to identify emergence of new strains. We hypothesize that MRSA strains are evolving with ongoing acquisition of SCC elements. This study was carried out to evaluate the evolution of MRSA at a tertiary care facility in Saudi Arabia.
MRSA isolates associated with invasive clinical infection, which were identified in 2017 at the microbiology laboratory, King Khalid University Hospital (KKUH) in Riyadh, Saudi Arabia, were studied. The molecular characterization of isolates was carried out using StaphyType DNA microarray (Alere Technologies GmbH/Abbott, Jena, Germany).
The 125 MRSA isolates studied belonged to 18 clonal complexes (CC) which were distributed into 32 strain assignments. The predominant CC were CC5 (n=30), CC6 (n=17), CC80 (n=13), CC22 (n=12), CC361 (n=12). The findings demonstrated the first identification of CC152, CC361 and CC1153 MRSA as well as ST5-MRSA-[I+fus], "Geraldine Clone", CC6-MRSA-IV (PVL+) and CC88-MRSA-V (PVL+), WA MRSA-117 in Saudi Arabia. Four novel variants were identified: CC5-MRSA-[VI+fus+tirS], CC22-MRSA-V/VT+fus, CC152-MRSA-V+fus and CC361-MRSA-[VT+fus]. Fifty-four isolates (n/N=54/125; 43.2%) including the novel strains carried the Q6GD50 SCC gene while the Panton-Valentine leukocidin genes were present in 30.4% (n/N=38/125).
The findings demonstrate an expanding MRSA repertoire in our setting including emergence of previously unreported clonal complexes and novel strains. The high carriage of gene suggests a role for fusidic acid misuse in driving the evolution of the MRSA genome and underscores the need for increased monitoring of antibiotic use.
需要持续监测耐甲氧西林金黄色葡萄球菌(MRSA)以识别新菌株的出现。我们假设MRSA菌株随着SCC元件的不断获得而进化。本研究旨在评估沙特阿拉伯一家三级医疗机构中MRSA的进化情况。
对2017年在沙特阿拉伯利雅得的国王哈立德大学医院(KKUH)微生物实验室鉴定出的与侵袭性临床感染相关的MRSA分离株进行研究。使用StaphyType DNA微阵列(德国耶拿的Alere Technologies GmbH/雅培公司)对分离株进行分子特征分析。
所研究的125株MRSA分离株属于18个克隆复合体(CC),分为32个菌株类型。主要的CC为CC5(n = 30)、CC6(n = 17)、CC80(n = 13)、CC22(n = 12)、CC361(n = 12)。研究结果首次在沙特阿拉伯鉴定出CC152、CC361和CC1153 MRSA以及ST5-MRSA-[I+fus]、“杰拉尔丁克隆”、CC6-MRSA-IV(PVL+)和CC88-MRSA-V(PVL+)、WA MRSA-117。鉴定出四个新变体:CC5-MRSA-[VI+fus+tirS]、CC22-MRSA-V/VT+fus、CC152-MRSA-V+fus和CC361-MRSA-[VT+fus]。54株分离株(n/N = 54/125;43.2%)包括新菌株携带Q6GD50 SCC基因,而Panton-Valentine杀白细胞素基因在30.4%(n/N = 38/125)的分离株中存在。
研究结果表明在我们的环境中MRSA种类在不断增加,包括出现以前未报告的克隆复合体和新菌株。基因的高携带率表明夫西地酸的不当使用在推动MRSA基因组进化中起作用,并强调需要加强对抗生素使用的监测。