Department of Microbiology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Gronostajowa 7, 30-387, Krakow, Poland.
Department of Molecular Microbiology, National Medicines Institute, Warsaw, Poland.
Eur J Clin Microbiol Infect Dis. 2020 Sep;39(9):1717-1725. doi: 10.1007/s10096-020-03893-w. Epub 2020 Apr 29.
Coagulase-negative staphylococci, ubiquitous commensals of human skin, and mucous membranes represent important pathogens for immunocompromised patients and neonates. The increasing antibiotic resistance among Staphylococcus epidermidis is an emerging problem worldwide. In particular, the linezolid-resistant S. epidermidis (LRSE) strains are observed in Europe since 2014. The aim of our study was to genetically characterize 11 LRSE isolates, recovered mostly from blood in the University Children's Hospital in Krakow, Poland, between 2015 and 2017. For identification of the isolates at the species level, we used 16S rRNA sequencing and RFLP of the saoC gene. Isolates were characterized phenotypically by determining their antimicrobial resistance patterns and using molecular methods such as PFGE, MLST, SCCmec typing, detection of the ica operon, and analysis of antimicrobial resistance determinants. All isolates were multidrug-resistant, including resistance to methicillin, and exhibited so-called PhLOPS phenotype. In PFGE, all isolates (excluding one from a catheter) represented identical patterns, were identified as ST2, and harbored the ica operon, responsible for biofilm formation. Linezolid resistance was associated with acquisition of A157R mutation in the ribosomal protein L3 and the presence of cfr gene. All isolates revealed new SCCmec cassette element composition. Recently, pediatric patients with serious staphylococcal infections are often treated with linezolid. The increasing linezolid resistance in bacterial strains becomes a real threat for patients, and monitoring such infections combined with surveillance and infection prevention programs is very important to decrease number of linezolid-resistant staphylococcal strains.
凝固酶阴性葡萄球菌是人类皮肤和黏膜的普遍共生菌,是免疫功能低下患者和新生儿的重要病原体。表皮葡萄球菌的抗生素耐药性日益增加是一个全球性的新兴问题。特别是,自 2014 年以来,欧洲已经观察到耐利奈唑胺的表皮葡萄球菌(LRSE)菌株。我们的研究目的是对 11 株从波兰克拉科夫大学儿童医院(University Children's Hospital in Krakow)的血液中分离出的耐利奈唑胺的表皮葡萄球菌(LRSE)分离株进行基因特征分析,这些分离株于 2015 年至 2017 年间分离得到。为了在种水平上鉴定这些分离株,我们使用 16S rRNA 测序和 saoC 基因的 RFLP 技术。通过确定其抗菌药物耐药模式,并使用分子方法(如 PFGE、MLST、SCCmec 分型、ica 操纵子检测和抗菌药物耐药决定因素分析),对分离株进行表型特征鉴定。所有分离株均为多药耐药株,包括对甲氧西林的耐药性,并表现出所谓的 PhLOPS 表型。在 PFGE 中,所有分离株(除了一个导管分离株外)均表现出相同的模式,被鉴定为 ST2 型,并携带 ica 操纵子,负责生物膜的形成。利奈唑胺耐药与核糖体蛋白 L3 的 A157R 突变和 cfr 基因的存在有关。所有分离株均揭示了新的 SCCmec 盒元件组成。最近,患有严重葡萄球菌感染的儿科患者通常使用利奈唑胺进行治疗。细菌菌株中利奈唑胺耐药性的增加对患者构成了真正的威胁,因此,监测此类感染并结合监测和感染预防计划非常重要,这有助于减少耐利奈唑胺的葡萄球菌菌株的数量。