Modes and modulations of antibiotic resistance gene expression

被引:266
作者
Depardieu, Florence
Podglajen, Isabelle
Leclercq, Roland
Collatz, Ekkehard
Courvalin, Patrice
机构
[1] Inst Pasteur, Unite Agents Antibacteriens, F-75724 Paris 15, France
[2] Univ Paris 06, INSERM U655, Lab Rech Mol Antibiot, Paris, France
[3] Univ Caen Basse Normandie, CHU Cote de Nacre, Microbiol Serv, Caen, France
[4] Univ Caen Basse Normandie, CHU Cote de Nacre, EA 2128, Caen, France
关键词
D O I
10.1128/CMR.00015-06
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Since antibiotic resistance usually affords a gain of function, there is an associated biological cost resulting in a loss of fitness of the bacterial host. Considering that antibiotic resistance is most often only transiently advantageous to bacteria, an efficient and elegant way for them to escape the lethal action of drugs is the alteration of resistance gene expression. It appears that expression of bacterial resistance to antibiotics is frequently regulated, which indicates that modulation of gene expression probably reflects a good compromise between energy saving and adjustment to a rapidly evolving environment. Modulation of gene expression can occur at the transcriptional or translational level following mutations or the movement of mobile genetic elements and may involve induction by the antibiotic. In the latter case, the antibiotic can have a triple activity: as an antibacterial agent, as an inducer of resistance to itself, and as an inducer of the dissemination of resistance determinants. We will review certain mechanisms, all reversible, that bacteria have elaborated to achieve antibiotic resistance by the fine-tuning of the expression of genetic information.
引用
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页码:79 / +
页数:38
相关论文
共 271 条
[1]   VanE-type vancomycin-resistant Enterococcus faecalis clinical isolates from Australia [J].
Abadía-Patiño, L ;
Christiansen, K ;
Bell, J ;
Courvalin, P ;
Périchon, B .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (12) :4882-4885
[2]   DNA interaction and phosphotransfer of the C4-dicarboxylate-responsive DcuS-DcuR two-component regulatory system from Escherichia coli [J].
Abo-Amer, AE ;
Munn, J ;
Jackson, K ;
Aktas, M ;
Golby, P ;
Kelly, DJ ;
Andrews, SC .
JOURNAL OF BACTERIOLOGY, 2004, 186 (06) :1879-1889
[3]   Characterization of a new efflux pump, MexGHI-OpmD, from Pseudomonas aeruginosa that confers resistance to vanadium [J].
Aendekerk, S ;
Ghysels, B ;
Cornelis, P ;
Baysse, C .
MICROBIOLOGY-SGM, 2002, 148 :2371-2381
[4]   Involvement of an active efflux system in the natural resistance of Pseudomonas aeruginosa to aminoglycosides [J].
Aires, JR ;
Köhler, T ;
Nikaido, H ;
Plésiat, P .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (11) :2624-2628
[5]   INDUCTION OF VANCOMYCIN RESISTANCE IN ENTEROCOCCUS-FAECIUM BY NON-GLYCOPEPTIDE ANTIBIOTICS [J].
ALLEN, NE ;
HOBBS, JN .
FEMS MICROBIOLOGY LETTERS, 1995, 132 (1-2) :107-114
[6]   Antimicrobial susceptibility and molecular characterization of community-acquired methicillin-resistant Staphylococcus aureus [J].
Almer, LS ;
Shortridge, VD ;
Nilius, AM ;
Beyer, JM ;
Soni, NB ;
Bui, MH ;
Stone, GG ;
Flamm, RK .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2002, 43 (03) :225-232
[7]   A NOVEL INTEGRON-LIKE ELEMENT CARRYING THE METALLO-BETA-LACTAMASE GENE BLA(IMP) [J].
ARAKAWA, Y ;
MURAKAMI, M ;
SUZUKI, K ;
ITO, H ;
WACHAROTAYANKUN, R ;
OHSUKA, S ;
KATO, N ;
OHTA, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (07) :1612-1615
[8]   blaCTX-M-2 is located in an unusual class 1 integron (In35) which includes Orf513 [J].
Arduino, SM ;
Roy, PH ;
Jacoby, GA ;
Orman, BE ;
Pineiro, SA ;
Centron, D .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (07) :2303-2306
[9]   vanC cluster of vancomycin-resistant Enterococcus gallinarum BM4174 [J].
Arias, CA ;
Courvalin, P ;
Reynolds, PE .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (06) :1660-1666
[10]   Characterization and modelling of VanT:: a novel, membrane-bound, serine racemase from vancomycin-resistant Enterococcus gallinarum BM4174 [J].
Arias, CA ;
Martín-Martinez, M ;
Blundell, TL ;
Arthur, M ;
Courvalin, P ;
Reynolds, PE .
MOLECULAR MICROBIOLOGY, 1999, 31 (06) :1653-1664