Infections caused by Gram-positive bacteria: a review of the global challenge

被引:317
作者
Woodford, Neil [1 ]
Livermore, David M. [1 ]
机构
[1] Hlth Protect Agcy, Ctr Infect, ARMRL, London NW9 5EQ, England
关键词
Antibiotic resistance; Enterococcus; Pneumococcus; Staphylococcus; RESISTANT STAPHYLOCOCCUS-AUREUS; FIELD GEL-ELECTROPHORESIS; PANTON-VALENTINE LEUKOCIDIN; IN-VITRO ACTIVITY; BETA-LACTAMASE GENE; 23S RIBOSOMAL-RNA; METHICILLIN-RESISTANT; ENTEROCOCCUS-FAECIUM; STREPTOCOCCUS-PNEUMONIAE; LINEZOLID-RESISTANT;
D O I
10.1016/S0163-4453(09)60003-7
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Infections caused by multidrug-resistant Gram-positive bacteria represent a major public health burden, not just in terms of morbidity and mortality, but also in terms of increased expenditure on patient management and implementation of infection control measures. Staphylococcus aureus and Enterococcus spp. are established pathogens in the hospital environment, and their frequent multidrug resistance complicates therapy. The archetypal hospital "superbug", methicillin-resistant S. aureus (MRSA), regularly attracts mass-media interest and, in many countries, there is political pressure to reduce MRSA infection rates, with some progress now being made in the United Kingdom and the United States. To compound these established problems, we have witnessed the emergence and spread of virulent clones of MRSA in the community, and of Clostridium difficile in hospitals. Multidrug-resistant Streptococcus pneumoniae clones are major community pathogens in many parts of the world, but are now being challenged by new conjugate vaccines. Using combinations of molecular epidemiological tools, which characterize the resistant isolates and their resistance determinants, scientists can track highly successful bacterial strains at local, national, and international levels. These methods have provided new insights into the evolution of key pathogens, and this information may aid the design of control strategies and vaccines. In addition, the development of new antimicrobials-including oxazolidinones, lipopeptides, glycylcyclines, ketolides, and new generations of fluoroquinolones, antistaphylococcal beta-lactams, and glycopeptides - must remain a high priority for the continued effective treatment of infections caused by resistant strains. So far, resistance to these newer agents is identified rarely in surveillance programs, but occasional reports of resistance causing therapeutic failure (e.g., with linezolid, daptomycin, telithromycin, or newer fluoroquinolones) give cause for concern. The emergence of antibiotic resistance is inevitable, but we must seek to decrease its impact and prolong the effectiveness of the agents available to us. (c) 2009 The British Infection Society. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:S4 / S16
页数:13
相关论文
共 176 条
[1]   Bactericidal activities of two daptomycin regimens against clinical strains of glycopeptide intermediate-resistant Staphylococcus aureus, vancomycin-resistant Enterococcus faecium, and methicillin-resistant Staphylococcus aureus isolates in an in vitro pharmacodynamic model with simulated endocardial vegetations [J].
Akins, RL ;
Rybak, MJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (02) :454-459
[2]   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
[3]  
[Anonymous], 1961, BMJ-BRIT MED J, V1, P113
[4]   Linezolid-resistant enterococci: report of the first isolates in the United Kingdom [J].
Auckland, C ;
Teare, L ;
Cooke, F ;
Kaufmann, ME ;
Warner, M ;
Jones, G ;
Bamford, K ;
Ayles, H ;
Johnson, AP .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 50 (05) :743-746
[5]   Pre- and postvaccination clonal compositions of invasive pneumococcal serotypes for isolates collected in the United States in 1999, 2001, and 2002 [J].
Beall, B ;
McEllistrem, MC ;
Gertz, RE ;
Wedel, S ;
Boxrud, DJ ;
Gonzalez, AL ;
Medina, MJ ;
Pai, R ;
Thompson, TA ;
Harrison, LH ;
McGee, L ;
Whitney, CG .
JOURNAL OF CLINICAL MICROBIOLOGY, 2006, 44 (03) :999-1017
[6]   Emergence of a novel penicillin-nonsusceptible, invasive serotype 35B clone of Streptococcus pneumoniae within the United States [J].
Beall, B ;
McEllistrem, MC ;
Gertz, RE ;
Boxrud, DJ ;
Besser, JM ;
Harrison, LH ;
Jorgensen, JH ;
Whitney, CG .
JOURNAL OF INFECTIOUS DISEASES, 2002, 186 (01) :118-122
[7]   Presence of Staphylococcus aureus with reduced susceptibility to vancomycin in Germany [J].
Bierbaum, G ;
Fuchs, K ;
Lenz, W ;
Szekat, C ;
Sahl, HG .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1999, 18 (10) :691-696
[8]   Antistaphylococcal activity of ceftobiprole, a new broad-spectrum cephalosporin [J].
Bogdanovich, T ;
Ednie, LM ;
Shapiro, S ;
Appelbaum, PC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (10) :4210-4219
[9]   Molecular characterization of Enterococcus faecalis N06-0364 with low-level vancomycin resistance harboring a novel D-Ala-D-Ser gene cluster, vanL [J].
Boyd, David A. ;
Willey, Barbara M. ;
Fawcett, Darlene ;
Gillani, Nazira ;
Mulvey, Michael R. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2008, 52 (07) :2667-2672
[10]   A European study on the relationship between antimicrobial use and antimicrobial resistance [J].
Bronzwaer, SLAM ;
Cars, O ;
Buchholz, U ;
Mölstad, S ;
Goettsch, W ;
Veldhuijzen, IK ;
Kool, JL ;
Sprenger, MJW ;
Degener, JE .
EMERGING INFECTIOUS DISEASES, 2002, 8 (03) :278-282