Minimizing potential resistance: The molecular view

被引:43
作者
Courvalin, P
Trieu-Cuot, P
机构
[1] Inst Pasteur, Unite Agents Antibacteriens, F-75724 Paris 15, France
[2] Fac Med Necker Enfants Malad, Microbiol Lab, Paris, France
关键词
D O I
10.1086/321840
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The major contribution of molecular biology to the study of antibiotic resistance has been the elucidation of nearly all biochemical mechanisms of resistance and the routes for dissemination of genetic information among bacteria. In this review, we consider the potential contribution of molecular biology to counteracting the evolution of resistant bacteria. In particular, we emphasize the fact that fundamental approaches have had direct practical effects on minimizing potential resistance: by improving interpretation of resistance phenotypes, by providing more adequate human therapy, by fostering more prudent use of antibiotics, and by allowing the rational design of new drugs that evade existing resistance mechanisms or address unexploited targets.
引用
收藏
页码:S138 / S146
页数:9
相关论文
共 51 条
[1]   The biological cost of antibiotic resistance [J].
Andersson, DI ;
Levin, BR .
CURRENT OPINION IN MICROBIOLOGY, 1999, 2 (05) :489-493
[2]  
AROZ R, 2000, BIOCHEMISTRY-US, P1571
[3]   Novel ribosomal mutations affecting translational accuracy, antibiotic resistance and virulence of Salmonella typhimurium [J].
Björkman, J ;
Samuelsson, P ;
Andersson, DI ;
Hughes, D .
MOLECULAR MICROBIOLOGY, 1999, 31 (01) :53-58
[4]   Circularization of Tn916 is required for expression of the transposon-encoded transfer functions:: characterization of long tetracycline-inducible transcripts reading through the attachment site [J].
Celli, J ;
Trieu-Cuot, P .
MOLECULAR MICROBIOLOGY, 1998, 28 (01) :103-117
[5]  
CHASLUSDANCLA E, 1986, FEMS MICROBIOL LETT, V34, P265, DOI 10.1111/j.1574-6968.1986.tb01417.x
[6]   EMERGENCE OF AMINOGLYCOSIDE 3-N-ACETYLTRANSFERASE-IV IN ESCHERICHIA-COLI AND SALMONELLA-TYPHIMURIUM ISOLATED FROM ANIMALS IN FRANCE [J].
CHASLUSDANCLA, E ;
MARTEL, JL ;
CARLIER, C ;
LAFONT, JP ;
COURVALIN, P .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1986, 29 (02) :239-243
[7]   HIGH GENETIC HOMOLOGY BETWEEN PLASMIDS OF HUMAN AND ANIMAL ORIGINS CONFERRING RESISTANCE TO THE AMINOGLYCOSIDES GENTAMICIN AND APRAMYCIN [J].
CHASLUSDANCLA, E ;
POHL, P ;
MEURISSE, M ;
MARIN, M ;
LAFONT, JP .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1991, 35 (03) :590-593
[8]   Decreased susceptibility of Streptococcus pneumoniae to fluoroquinolones in Canada [J].
Chen, DK ;
McGeer, A ;
de Azavedo, JC ;
Low, DE .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (04) :233-239
[9]   UNCONSTRAINED BACTERIAL PROMISCUITY - THE TN916-TN1545 FAMILY OF CONJUGATIVE TRANSPOSONS [J].
CLEWELL, DB ;
FLANNAGAN, SE ;
JAWORSKI, DD .
TRENDS IN MICROBIOLOGY, 1995, 3 (06) :229-236
[10]   TRANSFER OF ANTIBIOTIC-RESISTANCE GENES BETWEEN GRAM-POSITIVE AND GRAM-NEGATIVE BACTERIA [J].
COURVALIN, P .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (07) :1447-1451