Mechanisms of Resistance and Clinical Relevance of Resistance to β-Lactams, Glycopeptides, and Fluoroquinolones

被引:142
作者
Rice, Louis B. [1 ]
机构
[1] Brown Univ, Dept Med, Warren Alpert Med Sch, Providence, RI 02912 USA
关键词
STAPHYLOCOCCUS-AUREUS INFECTIONS; SEQUENCE TYPE ST131; ENTEROCOCCUS-FAECIUM; GASTROINTESTINAL COLONIZATION; AMPICILLIN RESISTANCE; CELL-WALL; VANCOMYCIN; ANTIBIOTICS; EXPRESSION; EMERGENCE;
D O I
10.1016/j.mayocp.2011.12.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The widespread use of antibiotics has resulted in a growing problem of antimicrobial resistance in the community and hospital settings. Antimicrobial classes for which resistance has become a major problem include the beta-lactams, the glycopeptides, and the fluoroquinolones. In gram-positive bacteria, beta-lactam resistance most commonly results from expression of intrinsic low-affinity penicillin-binding proteins. In gram-negative bacteria, expression of acquired beta-lactamases presents a particular challenge owing to some natural spectra that include virtually all beta-lactam classes. Glycopeptide resistance has been largely restricted to nosocomial Enterococcus faecium strains, the spread of which is promoted by ineffective infection control mechanisms for fecal organisms and the widespread use of colonization-promoting antimicrobials (especially cephalosporins and antianaerobic antibiotics). Fluoroquinolone resistance in community-associated strains of Escherichia coli, many of which also express beta-lactamases that confer cephalosporin resistance, is increasingly prevalent. Economic and regulatory forces have served to discourage large pharmaceutical companies from developing new antibiotics, suggesting that the antibiotics currently on the market may be all that will be available for the coming decade. As such, it is critical that we devise, test, and implement antimicrobial stewardship strategies that are effective at constraining and, ideally, reducing resistance in human pathogenic bacteria. (C) 2012 Mayo Foundation for Medical Education and Research square Mayo Clin Proc. 2012;87(2)198-208
引用
收藏
页码:198 / 208
页数:11
相关论文
共 69 条
[2]   The role of antimicrobial use in the epidemiology of resistant pneumococci: A 10-year follow up [J].
Arason, Vilhjalmur A. ;
Sigurdsson, Johann A. ;
Erlendsdottir, Helga ;
Gudmundsson, Sigurdur ;
Kristinsson, Karl G. .
MICROBIAL DRUG RESISTANCE-MECHANISMS EPIDEMIOLOGY AND DISEASE, 2006, 12 (03) :169-176
[3]   Outer membrane profiles of clonally related Klebsiella pneumoniae isolates from clinical samples and activities of cephalosporins and carbapenems [J].
Ardanuy, C ;
Liñares, J ;
Domínguez, MA ;
Hernández-Allés, S ;
Benedi, VJ ;
Martínez-Martínez, L .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (07) :1636-1640
[4]   CHARACTERIZATION OF TN1546, A TN3-RELATED TRANSPOSON CONFERRING GLYCOPEPTIDE RESISTANCE BY SYNTHESIS OF DEPSIPEPTIDE PEPTIDOGLYCAN PRECURSORS IN ENTEROCOCCUS-FAECIUM BM4147 [J].
ARTHUR, M ;
MOLINAS, C ;
DEPARDIEU, F ;
COURVALIN, P .
JOURNAL OF BACTERIOLOGY, 1993, 175 (01) :117-127
[5]   Diversity of Staphylococcal Cassette Chromosome mec Elements in Predominant Methicillin-Resistant Staphylococcus aureus Clones in a Small Geographic Area [J].
Basset, Patrick ;
Senn, Laurence ;
Vogel, Valerie ;
Zanetti, Giorgio ;
Blanc, Dominique S. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2010, 54 (11) :4589-4595
[6]   Newer Beta-lactam Antibiotics: Doripenem, Ceftobiprole, Ceftaroline, and Cefepime [J].
Bazan, Jose A. ;
Martin, Stanley I. ;
Kaye, Kenneth M. .
MEDICAL CLINICS OF NORTH AMERICA, 2011, 95 (04) :743-+
[7]   Complete Nucleotide Sequence of Plasmid pTN48, Encoding the CTX-M-14 Extended-Spectrum β-Lactamase from an Escherichia coli O102-ST405 Strain [J].
Billard-Pomares, Typhaine ;
Tenaillon, Olivier ;
Le Nagard, Herve ;
Rouy, Zoe ;
Cruveiller, Stephane ;
Medigue, Claudine ;
Arlet, Guillaume ;
Denamur, Erick ;
Branger, Catherine .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2011, 55 (03) :1270-1273
[8]   Relationship between Vancomycin Trough Concentrations and Nephrotoxicity: a Prospective Multicenter Trial [J].
Bosso, John A. ;
Nappi, Jean ;
Rudisill, Celeste ;
Wellein, Marlea ;
Bookstaver, P. Brandon ;
Swindler, Jenna ;
Mauldin, Patrick D. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2011, 55 (12) :5475-5479
[9]   In Vitro Effect of qnrA1, qnrB1, and qnrS1 Genes on Fluoroquinolone Activity against Isogenic Escherichia coli Isolates with Mutations in gyrA and parC [J].
Briales, A. ;
Rodriguez-Martinez, J. M. ;
Velasco, C. ;
Diaz de Alba, P. ;
Dominguez-Herrera, J. ;
Pachon, J. ;
Pascual, A. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2011, 55 (03) :1266-1269
[10]   Genetic linkage and cotransfer of a novel, vanB-containing transposon (Tn5382) and a low-affinity penicillin-binding protein 5 gene in a clinical vancomycin-resistant Enterococcus faecium isolate [J].
Carias, LL ;
Rudin, SD ;
Donskey, CJ ;
Rice, LB .
JOURNAL OF BACTERIOLOGY, 1998, 180 (17) :4426-4434