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Resistance to linezolid is mediated by the cfr gene in the first report of an outbreak of linezolid-resistant Staphylococcus aureus

机译:利奈唑胺耐药金黄色葡萄球菌暴发的首例报道是由cfr基因介导的对利奈唑胺的耐药性

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摘要

From April through June 2008, we identified 12 patients in the intensive care unit and 3 patients on other wards infected with methicillin-resistant Staphylococcus aureus that was also resistant to linezolid. We investigated the mechanism of resistance--point mutations in domain V of 23S ribosomal RNA (rRNA) or presence of the cfr gene--involved in the outbreak. Strains for the study were obtained in the intensive care unit and other wards. Minimal inhibitory concentrations were determined using automated methods, the E-test, or dilution in Mueller-Hinton agar in accordance with Clinical and Laboratory Standards Institute guidelines. Strains were genotyped using pulsed-field gel electrophoresis and were sequenced to determine the presence of point mutations in 23S rRNA. The presence of the cfr gene was determined by specific polymerase chain reaction. The result was that the minimal inhibitory concentrations of linezolid ranged from 16 mg/L to 32 mg/L, and all the strains were susceptible to tigecycline, vancomycin, and daptomycin. Typing of strains sequentially isolated by pulsed-field gel electrophoresis showed that each patient carried only 1 clonal type of linezolid-resistant, methicillin-resistant S. aureus as detected by sequential isolations. The presence of the cfr gene was confirmed in all the isolates. Furthermore, sequencing of domain V of 23S rRNA showed that the most common mechanism of linezolid resistance reported to date, mutation G2576T, was not detected in any of the strains analyzed. In conclusion, we report the presence of the cfr gene underlying the resistance mechanism involved in a clinical outbreak of linezolid-resistant S. aureus.
机译:从2008年4月到2008年6月,我们确定了重症监护病房的12名患者和其他病房的3名患者,这些患者感染了耐甲氧西林的金黄色葡萄球菌,并且对利奈唑胺也有抵抗力。我们调查了抗药性的机制-涉及爆发的23S核糖体RNA(rRNA)的V结构域中的点突变或cfr基因的存在。在重症监护室和其他病房中获得了用于研究的菌株。根据临床和实验室标准协会的指南,使用自动化方法,E检验或在Mueller-Hinton琼脂中稀释确定最小抑菌浓度。使用脉冲场凝胶电泳对菌株进行基因分型,并测序以确定在23S rRNA中存在点突变。 cfr基因的存在是通过特异性聚合酶链反应确定的。结果是,利奈唑胺的最低抑菌浓度范围为16 mg / L至32 mg / L,并且所有菌株均对替加环素,万古霉素和达托霉素敏感。通过脉冲场凝胶电泳顺序分离的菌株的分型显示,通过顺序分离检测,每位患者仅携带一种抗利奈唑胺,耐甲氧西林金黄色葡萄球菌的克隆型。在所有分离物中都证实了cfr基因的存在。此外,对23S rRNA的结构域V进行测序表明,迄今为止,在所分析的任何菌株中均未检测到最常见的利奈唑胺抗性机制突变G2576T。总而言之,我们报告了在临床上对利奈唑胺耐药的金黄色葡萄球菌的耐药机制中涉及抗药机制的cfr基因的存在。

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