Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at the University of California, Los Angeles, California, USA.
Clin Microbiol Rev. 2013 Oct;26(4):759-80. doi: 10.1128/CMR.00030-13.
Daptomycin is a lipopeptide antimicrobial with in vitro bactericidal activity against Gram-positive bacteria that was first approved for clinical use in 2004 in the United States. Since this time, significant data have emerged regarding the use of daptomycin for the treatment of serious infections, such as bacteremia and endocarditis, caused by Gram-positive pathogens. However, there are also increasing reports of daptomycin nonsusceptibility, in Staphylococcus aureus and, in particular, Enterococcus faecium and Enterococcus faecalis. Such nonsusceptibility is largely in the context of prolonged treatment courses and infections with high bacterial burdens, but it may occur in the absence of prior daptomycin exposure. Nonsusceptibility in both S. aureus and Enterococcus is mediated by adaptations to cell wall homeostasis and membrane phospholipid metabolism. This review summarizes the data on daptomycin, including daptomycin's unique mode of action and spectrum of activity and mechanisms for nonsusceptibility in key pathogens, including S. aureus, E. faecium, and E. faecalis. The challenges faced by the clinical laboratory in obtaining accurate susceptibility results and reporting daptomycin MICs are also discussed.
达托霉素是一种脂肽类抗菌药物,具有体外杀菌活性,可杀灭革兰氏阳性菌,于 2004 年首次在美国获准临床应用。自那时以来,大量数据表明达托霉素可用于治疗革兰氏阳性病原体引起的严重感染,如菌血症和心内膜炎。然而,达托霉素耐药性的报告也越来越多,包括金黄色葡萄球菌,尤其是屎肠球菌和粪肠球菌。这种耐药性主要与延长治疗疗程和高细菌负荷感染有关,但也可能在没有达托霉素暴露的情况下发生。金黄色葡萄球菌和肠球菌的耐药性是通过适应细胞壁内稳态和膜磷脂代谢来介导的。本综述总结了达托霉素的相关数据,包括达托霉素独特的作用模式和作用谱,以及关键病原体(包括金黄色葡萄球菌、屎肠球菌和粪肠球菌)产生耐药性的机制。还讨论了临床实验室在获得准确药敏结果和报告达托霉素 MIC 方面面临的挑战。