Diversity of β-lactam resistance mechanisms in cystic fibrosis isolates of Pseudomonas aeruginosa: a French multicentre study

被引:59
作者
Llanes, Catherine [1 ]
Pourcel, Christine [2 ]
Richardot, Charlotte [1 ]
Plesiat, Patrick [1 ]
Fichant, Gwennaele [3 ]
Cavallo, Jean-Didier [4 ]
Merens, Audrey [5 ]
机构
[1] CHRU Jean Minjoz, Ctr Natl Reference Resistance Antibiot, Besancon, France
[2] Univ Paris 11, Inst Genet & Microbiol, F-91405 Orsay, France
[3] CNRS, Lab Genet & Microbiol Mol, Toulouse, France
[4] Ecole Val de Grace, Paris, France
[5] Hop Instruct Armees Begin, Serv Biol Med, St Mande, France
关键词
OprD; efflux systems; AmpC; antibiotic resistance surveillance; molecular typing; MULTIDRUG EFFLUX SYSTEM; MEXE-MEXF-OPRN; ANTIMICROBIAL SUSCEPTIBILITY; CARBAPENEM RESISTANCE; SEQUENCE ALIGNMENT; CLINICAL STRAINS; EXPRESSION; INFECTION; EMERGENCE; REGION;
D O I
10.1093/jac/dkt115
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
To investigate the resistance mechanisms of -lactam-resistant Pseudomonas aeruginosa isolated from cystic fibrosis (CF) patients in France. Two-hundred-and-four P. aeruginosa CF isolates were collected in 10 French university hospitals in 2007. Their susceptibility to 14 antibiotics and their resistance mechanisms to -lactams were investigated. Their -lactamase contents were characterized by isoelectric focusing, PCR and enzymatic assays. Expression levels of efflux pumps and the intrinsic -lactamase AmpC were quantified by reverse transcription real-time quantitative PCR. Genotyping was performed using multiple-locus variable number of tandem repeats analysis (MLVA). The oprD genes were sequenced and compared with those of reference P. aeruginosa strains. To assess deficient OprD production, western blotting experiments were carried out on outer membrane preparations. MLVA typing discriminated 131 genotypes and 47 clusters. One-hundred-and-twenty-four isolates (60.8) displayed a susceptible phenotype to -lactams according to EUCAST breakpoints. In the 80 remaining isolates, resistance to -lactams resulted from derepression of intrinsic cephalosporinase AmpC (61.3) and/or acquisition of secondary -lactamases (13.8). Efflux pumps were up-regulated in 88.8 of isolates and porin OprD was lost in 53.8 of isolates due to frameshifting or nonsense mutations in the oprD gene. beta-Lactam resistance rates are quite high in CF strains of P. aeruginosa isolated in France and not really different from those reported for nosocomial strains. Development of -lactam resistance is correlated with patient age. It results from intrinsic mechanisms sequentially accumulated by bacteria isolated from patients who have undergone repeated courses of chemotherapy.
引用
收藏
页码:1763 / 1771
页数:9
相关论文
共 52 条
[11]   THE ABSENCE OF CORRELATION BETWEEN ALLOZYME AND RRN RFLP ANALYSIS INDICATES A HIGH GENE FLOW-RATE WITHIN HUMAN CLINICAL PSEUDOMONAS-AERUGINOSA ISOLATES [J].
DENAMUR, E ;
PICARD, B ;
DECOUX, G ;
DENIS, JB ;
ELION, J .
FEMS MICROBIOLOGY LETTERS, 1993, 110 (03) :275-280
[12]   Antimicrobial resistance of Pseudomonas aeruginosa biofilms [J].
Drenkard, E .
MICROBES AND INFECTION, 2003, 5 (13) :1213-1219
[13]   Analysis of antibiotic resistance gene expression in Pseudomonas aeruginosa by quantitative real-time-PCR [J].
Dumas, JL ;
van Delden, C ;
Perron, K ;
Köhler, T .
FEMS MICROBIOLOGY LETTERS, 2006, 254 (02) :217-225
[14]   Acquisition of different carbapenem resistance mechanisms by an epidemic clonal lineage of Pseudomonas aeruginosa [J].
Edalucci, E. ;
Spinelli, R. ;
Dolzani, L. ;
Riccio, M. Letizia ;
Dubois, V. ;
Tonin, E. Angelo ;
Rossolini, G. M. ;
Lagatolla, C. .
CLINICAL MICROBIOLOGY AND INFECTION, 2008, 14 (01) :88-90
[15]   MUSCLE: multiple sequence alignment with high accuracy and high throughput [J].
Edgar, RC .
NUCLEIC ACIDS RESEARCH, 2004, 32 (05) :1792-1797
[16]   C-terminal region of Pseudomonas aeruginosa outer membrane porin OprD modulates susceptibility to meropenem [J].
Epp, SF ;
Köhler, T ;
Plesiat, P ;
Michea-Hamzehpour, M ;
Frey, J ;
Pechère, JC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (06) :1780-1787
[17]   BIONJ: An improved version of the NJ algorithm based on a simple model of sequence data [J].
Gascuel, O .
MOLECULAR BIOLOGY AND EVOLUTION, 1997, 14 (07) :685-695
[18]   RAPID EMERGENCE OF RESISTANCE IN PSEUDOMONAS-AERUGINOSA IN CYSTIC-FIBROSIS PATIENTS DUE TO INVIVO SELECTION OF STABLE PARTIALLY DEREPRESSED BETA-LACTAMASE PRODUCING STRAINS [J].
GIWERCMAN, B ;
LAMBERT, PA ;
ROSDAHL, VT ;
SHAND, GH ;
HOIBY, N .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1990, 26 (02) :247-259
[19]   CORRELATION BETWEEN LIPOPOLYSACCHARIDE STRUCTURE AND PERMEABILITY RESISTANCE IN BETA-LACTAM-RESISTANT PSEUDOMONAS-AERUGINOSA [J].
GODFREY, AJ ;
HATLELID, L ;
BRYAN, LE .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1984, 26 (02) :181-186
[20]   BETA-LACTAM-RESISTANT PSEUDOMONAS-AERUGINOSA WITH MODIFIED PENICILLIN-BINDING PROTEINS EMERGING DURING CYSTIC-FIBROSIS TREATMENT [J].
GODFREY, AJ ;
BRYAN, LE ;
RABIN, HR .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1981, 19 (05) :705-711