Mechanisms of antibiotic resistance in enterococci

被引:493
作者
Miller, William R. [1 ]
Munita, Jose M. [1 ,2 ,3 ]
Arias, Cesar A. [1 ,4 ]
机构
[1] Univ Texas Med Sch, Div Infect Dis, Dept Internal Med, Houston, TX 77030 USA
[2] Clin Alemana Santiago, Santiago, Chile
[3] Univ Desarrollo, Santiago, Chile
[4] Univ El Bosque, Mol Genet & Antimicrobial Resistance Unit, Bogota, Colombia
关键词
antimicrobial resistance; enterococcus; mechanisms of resistance; vancomycin-resistant enterococci; BETA-LACTAM RESISTANCE; PENICILLIN-BINDING PROTEIN; INTRINSIC CEPHALOSPORIN RESISTANCE; FAECALIS INFECTIVE ENDOCARDITIS; PLASMID-MEDIATED RESISTANCE; GROUP-D STREPTOCOCCI; STAPHYLOCOCCUS-AUREUS; VANCOMYCIN RESISTANCE; AMPICILLIN RESISTANCE; IN-VITRO;
D O I
10.1586/14787210.2014.956092
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Multidrug-resistant (MDR) enterococci are important nosocomial pathogens and a growing clinical challenge. These organisms have developed resistance to virtually all antimicrobials currently used in clinical practice using a diverse number of genetic strategies. Due to this ability to recruit antibiotic resistance determinants, MDR enterococci display a wide repertoire of antibiotic resistance mechanisms including modification of drug targets, inactivation of therapeutic agents, overexpression of efflux pumps and a sophisticated cell envelope adaptive response that promotes survival in the human host and the nosocomial environment. MDR enterococci are well adapted to survive in the gastrointestinal tract and can become the dominant flora under antibiotic pressure, predisposing the severely ill and immunocompromised patient to invasive infections. A thorough understanding of the mechanisms underlying antibiotic resistance in enterococci is the first step for devising strategies to control the spread of these organisms and potentially establish novel therapeutic approaches.
引用
收藏
页码:1221 / 1236
页数:16
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