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

被引:110
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
相关论文
共 55 条
[1]   Emergence of high-level vancomycin-resistant Staphylococcus aureus in the Imam Khomeini hospital in Tehran [J].
Aligholi, Marzieh ;
Emaneini, Mohammad ;
Jabalameli, Fereshteh ;
Shahsavan, Shadi ;
Dabiri, Hosein ;
Sedaght, Hossein .
MEDICAL PRINCIPLES AND PRACTICE, 2008, 17 (05) :432-434
[2]   Vancomycin MICs did not creep in Staphylococcus aureus isolates from 2002 to 2006 in a setting with low vancomycin usage [J].
Alos, Juan-Ignacio ;
Garcia-Canas, Ana ;
Garcia-Hierro, Paloma ;
Rodriguez-Salvanes, Francisco .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2008, 62 (04) :773-775
[3]   Reduced glycopeptide susceptibility in methicillin-resistant Staphylococcus aureus (MRSA) [J].
Appelbaum, Peter C. .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2007, 30 (05) :398-408
[4]   Clinical and microbiological aspects of linezolid resistance mediated by the cfr gene encoding a 23S rRNA methyltransferase [J].
Arias, Cesar A. ;
Vallejo, Martha ;
Reyes, Jinnethe ;
Panesso, Diana ;
Moreno, Jaime ;
Castaneda, Elizabeth ;
Villegas, Maria V. ;
Murray, Barbara E. ;
Quinn, John P. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2008, 46 (03) :892-896
[5]   Linezolid resistance in Staphylococcus aureus:: Gene dosage effect, stability, fitness costs, and cross-resistances [J].
Besier, Silke ;
Ludwig, Albrecht ;
Zander, Johannes ;
Brade, Volker ;
Wichelhaus, Thomas A. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2008, 52 (04) :1570-1572
[6]  
BONILLA H, 2009, 49 INT C ANT AG CHEM
[7]   Perspectives on daptomycin resistance, with emphasis on resistance in Staphylococcus aureus [J].
Boucher, Helen W. ;
Sakoulas, George .
CLINICAL INFECTIOUS DISEASES, 2007, 45 (05) :601-608
[8]   Oxazolidinones: activity, mode of action, and mechanism of resistance [J].
Bozdogan, B ;
Appelbaum, PC .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2004, 23 (02) :113-119
[9]   Update of the in vitro activity of daptomycin tested against 6710 Gram-positive cocci isolated in North America (2006) [J].
Castanheira, Mariana ;
Jones, Ronald N. ;
Sader, Helio S. .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2008, 61 (02) :235-239
[10]   Clinical features associated with bacteremia due to heterogeneous vancomycin-intermediate Staphylococcus aureus [J].
Charles, PGP ;
Ward, PB ;
Johnson, PDR ;
Howden, BP ;
Grayson, ML .
CLINICAL INFECTIOUS DISEASES, 2004, 38 (03) :448-451