Role of outer membrane protein OprD and penicillin-binding proteins in resistance of Pseudomonas aeruginosa to imipenem and meropenem

被引:78
作者
Farra, Anna [2 ]
Islam, Sohidul [1 ]
Stralfors, Annelie [1 ]
Sorberg, Mikael [2 ]
Wretlind, Bengt [1 ]
机构
[1] Karolinska Univ Hosp, Karolinska Inst, Dept Lab Med, Div Clin Microbiol, SE-14186 Stockholm, Sweden
[2] Karolinska Univ Hosp, Karolinska Inst, Dept Infect Dis, Div Internal Med, SE-17176 Stockholm, Sweden
关键词
Pseudomonas aeruginosa; imipenem; OprD; penicillin-binding proteins;
D O I
10.1016/j.ijantimicag.2007.12.016
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The main mechanism of imipenem resistance in Pseudomonas aeruginosa is via downregulation of the gene for OprD porin. In a previous study, it was shown that the level of resistance did not parallel with the degree of downregulation of the porin gene, thus arguing for the existence of other resistance mechanisms. Penicillin-binding protein (PBP) 2 and PBP3 are involved in carbapenem resistance in Escherichia coli. The genes for PBPs were sequenced in three imipenem-resistant clinical strains and these strains were conjugated with two susceptible P. aeruginosa PA0 strains, selecting for auxotrophic markers. In all the clinical and resistant isolates there was no obvious elevation of AmpC cephalosporinase. The active sites of PBP1b (ponB), PBP2 (pbpA), PBP3 (pbpB) and PBP6 (dacC) had no mutations in any of the examined strains. Production of oprD mRNA was significantly lower in clinical strains and transconjugants after selection for the proB marker (PA4565 at 5113 kb). The clinical strains had alterations in OprD that were not found in transconjugants. Our findings suggest that PBPs do not play a role in imipenem resistance in the clinical strains examined here, but that a regulatory gene for oprD contributing to carbapenem resistance is located close to the proB gene. (C) 2008 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:427 / 433
页数:7
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