The threat of antibiotic resistance in Gram-negative pathogenic bacteria:: β-lactams in peril!

被引:166
作者
Thomson, JM
Bonomo, RA
机构
[1] Case Western Reserve Univ, Dept Pharmacol, Sch Med, Cleveland, OH 44106 USA
[2] Louis Stokes Cleveland Vet Affairs Med Ctr, Dept Med, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.mib.2005.08.014
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
beta-Lactam antibiotics are the cornerstone of our antibiotic armamentarium. By inhibiting bacterial cell wall synthesis, they are highly effective against Gram-positive and Gram-negative bacteria. Unfortunately, bacteria have evolved sophisticated resistance mechanisms to combat the lethal effects of beta-lactam antibiotics. Pseudomonas aeruginosa, Acinetobacter baumannii and Klebsiella pneumoniae are all able to evade killing by penicillins, cephalosporins and carbapenems. This multi-drug resistant phenotype that challenges healthcare workers worldwide is caused by an array of resistance determinants. These include altered expression of outer membrane proteins and efflux pumps, along with an increasing arsenal of beta-lactamases. Future strategies in beta-lactam design must take into account the complex nature of resistance in Gram-negative pathogens.
引用
收藏
页码:518 / 524
页数:7
相关论文
共 52 条
[21]   Evaluation of colistin as an agent against multi-resistant in Gram-negative bacteria [J].
Li, J ;
Nation, RL ;
Milne, RW ;
Turnidge, JD ;
Coulthard, K .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2005, 25 (01) :11-25
[22]   Interplay between the MexA-MexB-OprM multidrug efflux system and the outer membrane barrier in the multiple antibiotic resistance of Pseudomonas aeruginosa [J].
Li, XZ ;
Zhang, L ;
Poole, K .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2000, 45 (04) :433-436
[23]   First isolation of metallo-β-lactamase-producing multiresistant Klebsiella pneumoniae from a patient in Brazil [J].
Lincopan, N ;
McCulloch, JA ;
Reinert, C ;
Cassettari, VC ;
Gales, AC ;
Mamizuka, EM .
JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (01) :516-519
[24]   Multiple mechanisms of antimicrobial resistance in Pseudomonas aeruginosa:: Our worst nightmare? [J].
Livermore, DM .
CLINICAL INFECTIOUS DISEASES, 2002, 34 (05) :634-640
[25]   BETA-LACTAMASES IN LABORATORY AND CLINICAL RESISTANCE [J].
LIVERMORE, DM .
CLINICAL MICROBIOLOGY REVIEWS, 1995, 8 (04) :557-&
[26]   Clinical strains of Pseudomonas aeruginosa overproducing MexAB-OprM and MexXY efflux pumps simultaneously [J].
Llanes, C ;
Hocquet, D ;
Vogne, C ;
Benali-Baitich, D ;
Neuwirth, C ;
Plésiat, P .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (05) :1797-1802
[27]   First nosocomial outbreak of Pseudomonas aeruginosa producing an integron-borne metallo-β-lactamase (VIM-2) in the United States [J].
Lolans, K ;
Queenan, AM ;
Bush, K ;
Sahud, A ;
Quinn, JP .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (08) :3538-3540
[28]   Vacuuming the periplasm [J].
Lomovskaya, O ;
Totrov, M .
JOURNAL OF BACTERIOLOGY, 2005, 187 (06) :1879-1883
[29]   Resistance-nodulation-cell division-type efflux pump involved in aminoglycoside resistance in Acinetobacter baumannii strain BM4454 [J].
Magnet, S ;
Courvalin, P ;
Lambert, T .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (12) :3375-3380
[30]   Expression of the RND-type efflux pump AdeABC in Acinetobacter baumannii is regulated by the AdeRS two-component system [J].
Marchand, I ;
Damier-Piolle, L ;
Courvalin, P ;
Lambert, T .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (09) :3298-3304