Monitoring of the Pseudomonas aeruginosa sensitivity to antibiotics in France and spreading of betalactamine resistance mechanisms:: GERPB 1999 study

被引:16
作者
Cavallo, JD
Leblanc, F
Fabre, R
Fourticq-Esqueöute, A
机构
[1] Hop Instruct Armees Begin, Serv Biol Med, F-94163 St Mande, France
[2] Lab Glaxo Smithkline, Marly Le Roi, France
来源
PATHOLOGIE BIOLOGIE | 2001年 / 49卷 / 07期
关键词
France; Pseudomonas aeruginosa; resistance mechanisms; susceptibility to antibiotics;
D O I
10.1016/S0369-8114(01)00213-9
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
A prospective survey was carried out in october 1999 in 15 french teaching hospitals. Average susceptibility rates, determined by minimal inhibitory concentrations, for the 738 non-repetitive strains of R aeruginosa isolated were: ticarcillin, 58%, ticarcillin + clavulanic acid, 56%, piperacillin, 73%, piperacillin + tazobactam, 82%, ceftazidime, 76%, cefepime, 53%, cetpirome, 36%, aztreonam, 58%, imipenem, 81%, amikacin, 62%, tobramycine, 71% and, ciprofloxacin, 60%. Among the 75% serotypable strains, the most frequent serotypes were, O : 6 (15.3%), O : 11 (14.5%), O : 1 (10.4%), O : 3 (7.9%), O : 4 (6.1%) and O : 12 (6.1%). The serotype O : 12 was the most resistant to antibiotics. Forty-two percent of the strains were resistant or presented an intermediate susceptibility to ticarcillin. Mechanisms were as follow: 14.5% non enzymatic mechanism, 12.5% overproduction of the constitutive cephalosporinase, 7.1% transferable betalactamase and, 6.9% combination of these mechanisms. Among the 67 transferable betalactamases: 48 (71.6%) were PSE-1, 12 (19.4%) TEM-2 and 6 (7.5%) oxacillinases. One extended spectrum betalactamase was characterized, Among the cephalosporines tested, cefepime was less affected by the overproduction of constitutive cephalosporinase. Ceftazidime, remained the best cephalosporin except against the strains overexpressing the chromosomal type 1 beta-lactamase. Resistance to tobramycin was mainly due to enzymatic mechanisms with a high level of resistance. Decreased susceptibility was more frequent for amikacin than for tobramycin. This was probably related with non enzymatic mechanisms. (C) 2001 Editions scientifiques et medicales Elsevier SAS.
引用
收藏
页码:534 / 539
页数:6
相关论文
共 15 条
[1]  
ACAR J, 1998, PATHOL BIOL, V46, P1
[2]   Comparitive distribution of resistance patterns and serotypes in Pseudomonas aeruginosa isolates from intensive care units and other wards [J].
Bert, F ;
LambertZechovsky, N .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1996, 37 (04) :809-813
[3]   Regional survey of Pseudomonas aeruginosa in northern France:: epidemiological and microbiological data. [J].
Cattoen, C ;
Levent, T ;
Grandbastien, B ;
Descamps, D ;
Bouillet, L ;
Coignard, B ;
Beaucaire, G .
MEDECINE ET MALADIES INFECTIEUSES, 1999, 29 (03) :160-166
[4]  
Cavallo JD, 2000, PATHOL BIOL, V48, P472
[5]   Hospital outbreak of carbapenem-resistant Pseudomonas aeruginosa producing VIM-1, a novel transferable metallo-β-lactamase [J].
Cornaglia, G ;
Mazzariol, A ;
Lauretti, L ;
Rossolini, GM ;
Fontana, R .
CLINICAL INFECTIOUS DISEASES, 2000, 31 (05) :1119-1125
[6]  
COURVALIN P, 1996, CLIN MICROBIOL INFEC, V2, P511
[7]  
*GERPD, 2000, LETT INFECT, V15, P18
[8]   Substrate specificities of MexAB-OprM, MexCD-OprJ, and MexXY-OprM efflux pumps in Pseudomonas aeruginosa [J].
Masuda, N ;
Sakagawa, E ;
Ohya, S ;
Gotoh, N ;
Tsujimoto, H ;
Nishino, T .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (12) :3322-3327
[9]  
Pechere Jean-Claude, 1999, Clin Microbiol Infect, V5 Suppl 1, pS15, DOI 10.1111/j.1469-0691.1999.tb00719.x
[10]  
Philippon A, 1998, MED MALADIES INFECT, V28, P134