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首页> 外文期刊>APMIS: Acta Pathologica, Microbiologica et Immunologica Scandinavica >Emergence of mutation-based linezolid-resistant invasive Enterococcus faecalis in a haemodialysis patient in Norway
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Emergence of mutation-based linezolid-resistant invasive Enterococcus faecalis in a haemodialysis patient in Norway

机译:在挪威的血液透析患者中​​出现基于突变的耐利奈唑胺类侵入性肠球菌的出现

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摘要

Linezolid, an oxazolidinone antibiotic, has been available as a therapeutic alternative against antibiotic-resistant Gram-positive cocci since 2000. Linezolid inhibits bacterial protein synthesis by binding to the A site pocket at the ribosomal peptidyltransferase centre in domain V of the 23S rRNA genes. Point mutations in this region, in particular a G2576U mutation, have been associated with linezolid resistance in both enterococci and staphylococci [1, 2]. Recently, the first Enterococcus human isolate with plasmid mediated transferable linezolid resistance encoded by the cfr (chloramphenicol-florfenicol resistance) gene was recovered from a patient in Thailand [3]. Although resistance to linezolid in clinical isolates was reported prior to the release of the drug [4], surveillance programmes in both the US and Europe confirm that resistance rates remain very low [1, 2].
机译:利奈唑胺是一种恶唑烷酮抗生素,自2000年以来就可以用作抗药性革兰氏阳性球菌的治疗替代品。利奈唑胺通过结合23S rRNA基因V域中核糖体肽基转移酶中心的A位点口袋来抑制细菌蛋白质合成。该区域的点突变,特别是G2576U突变,已与肠球菌和葡萄球菌中的利奈唑胺抗性相关[1、2]。最近,从泰国的一名患者中回收了首个肠球菌人类分离株,该分离株具有由质粒介导的由cfr(氯霉素-氟苯尼考耐药)基因编码的可转移利奈唑胺耐药性[3]。尽管在药物释放之前已有临床分离株对利奈唑胺产生耐药性的报道[4],但美国和欧洲的监测计划均证实耐药率仍然很低[1、2]。

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