Pillai Satish K, Gold Howard S, Sakoulas George, Wennersten Christine, Moellering Robert C, Eliopoulos George M
Department of Infectious Disease, Cleveland Clinic Foundation, Mailstop S32, Cleveland, OH 44195, USA.
Antimicrob Agents Chemother. 2007 Jun;51(6):2223-5. doi: 10.1128/AAC.00202-07. Epub 2007 Apr 2.
A previous study documented the presence of mutations in mprF that accompanied the loss of daptomycin susceptibility among Staphylococcus aureus isolates following exposure to the drug. An association between the development of glycopeptide-intermediate S. aureus and daptomycin nonsusceptibility has also been recently described. We report that among three clinical S. aureus isolates which developed vancomycin heteroresistance, as well as daptomycin nonsusceptibility despite a lack of exposure to this drug, there were no mutations resulting in amino acid substitutions in MprF.
先前的一项研究记录了在金黄色葡萄球菌分离株接触达托霉素后,mprF中存在的突变伴随着达托霉素敏感性的丧失。最近也有人描述了耐糖肽金黄色葡萄球菌的出现与达托霉素不敏感性之间的关联。我们报告,在三株出现万古霉素异质性耐药以及尽管未接触过该药物但对达托霉素不敏感的临床金黄色葡萄球菌分离株中,MprF没有导致氨基酸替代的突变。