Resistance or decreased susceptibility to glycopeptides, daptomycin, and linezolid in methicillin-resistant Staphylococcus aureus

被引:107
|
作者
Nannini, Esteban [2 ]
Murray, Barbara E. [1 ,4 ]
Arias, Cesar A. [1 ,3 ,5 ]
机构
[1] Univ Texas Med Sch, Dept Internal Med, Div Infect Dis, Ctr Study Emerging & Reemerging Pathogens, Houston, TX USA
[2] Univ Nacl Rosario, Div Infect Dis, Sch Med, RA-2000 Rosario, Santa Fe, Argentina
[3] Univ Texas Med Sch, Lab Antimicrobial Res, Houston, TX USA
[4] Univ Texas Med Sch, Lab Enterococcal Res, Houston, TX USA
[5] Mol Genet & Antimicrobial Resistance Unit, Bogota, Colombia
关键词
VANCOMYCIN-INTERMEDIATE; REDUCED SUSCEPTIBILITY; BACTERICIDAL ACTIVITY; 1ST REPORT; CFR GENE; ENDOCARDITIS; EFFICACY; STRAINS; ISOLATE; OXAZOLIDINONES;
D O I
10.1016/j.coph.2010.06.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Methicillin-resistant Staphylococcus aureus (MRSA) with decreased susceptibility to glycopeptides can be categorized as first, heteroresistant to vancomycin (hVISA); second, with intermediate susceptibility to vancomycin (VISA); and third, fully resistant to vancomycin (VRSA). Whereas the hVISA and VISA isolates are characterized by increased cell wall thickness, activated cell wall synthesis and reduced autolysis, VRSA harbor the vanA gene cluster resulting in a remodeled peptidoglycan. Nonsusceptibility to daptomycin has been associated with changes in the structure and function of the cell envelope and surface charge. Linezolid resistance in MRSA is often associated with mutations in the 23S rRNA, although resistance mediated by an acquired gene (cfr encoding a 23S rRNA methyltransferase) has now been documented in several continents and in outbreak settings.
引用
收藏
页码:516 / 521
页数:6
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