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Outer membrane proteins responsible for multiple drug resistance in Pseudomonas aeruginosa
1Biological Research Laboratories, Sankyo Co., Ltd., Tokyo, Japan.
Abstract:
Three types of multiple-drug-resistant mutants which were phenotypically similar to previously described nalB, nfxB, and nfxC mutants were isolated from Pseudomonas aeruginosa PAO1 and two clinical isolates. Type 1 (nalB-type) mutants showed cross-resistance to meropenem, cephems, and quinolones. They overproduced an outer membrane protein with an apparent molecular mass of 50 kDa (OprM). Type 2 (nfxB-type) mutants showed cross-resistance to quinolones and new cephems, i.e., cefpirome and cefozopran, concomitant with overproduction of an outer membrane protein with an apparent molecular mass of 54 kDa (OprJ). Type 3 (nfxC-type) mutants showed cross-resistance to carbapenems and quinolones. They produced decreased amounts of OprD and increased amounts of a 50-kDa protein (OprN), which was almost the same molecular weight as that of OprM, but it was distinguishable from OprM by its heat modifiability on sodium dodecyl sulfate-polyacrylamide gel electrophoresis. In the presence of salicylate, the parent strains showed an increased level of resistance to carbapenems and quinolones and produced decreased amounts of OprD and increased amounts of OprN. Salicylate caused the repression of OprJ production and the loss of resistance to cefpirome and cefozopran in two of the three OprJ-overproducing mutants, although salicylate slightly increased the level of resistance in the parent strains. The changes in susceptibilities were transient in the presence of salicylate. These data suggest that at least three different outer membrane proteins, OprM, OprJ, and OprN, are associated with multiple drug resistance in P. aeruginosa.
Insights
Three outer membrane proteins (OprM, OprJ, and OprN) in Pseudomonas aeruginosa are linked to multiple drug resistance. These proteins confer resistance to various antibiotics, including carbapenems and quinolones.
Area of Science:
- Microbiology
- Molecular Biology
- Biochemistry
Background:
- Pseudomonas aeruginosa is an opportunistic pathogen known for developing multidrug resistance.
- Understanding the mechanisms of this resistance is crucial for effective treatment strategies.
Purpose of the Study:
- To identify and characterize novel outer membrane proteins involved in multidrug resistance in Pseudomonas aeruginosa.
- To investigate the role of specific outer membrane proteins (OprM, OprJ, OprN) in conferring resistance to various antibiotic classes.
Main Methods:
- Isolation and characterization of multiple-drug-resistant mutants of Pseudomonas aeruginosa.
- Analysis of outer membrane protein expression using SDS-PAGE.
- Assessment of antibiotic susceptibility profiles.
- Investigation of the effect of salicylate on gene expression and antibiotic resistance.
Main Results:
- Three distinct types of multidrug-resistant mutants were identified, phenotypically resembling nalB, nfxB, and nfxC mutants.
- Type 1 mutants overproduced OprM, conferring resistance to meropenem, cephems, and quinolones.
- Type 2 mutants overproduced OprJ, conferring resistance to quinolones and new cephems.
- Type 3 mutants showed altered OprD and OprN expression, conferring resistance to carbapenems and quinolones.
Conclusions:
- At least three distinct outer membrane proteins (OprM, OprJ, and OprN) are associated with multiple drug resistance in Pseudomonas aeruginosa.
- These proteins play a significant role in the bacterium's ability to resist a range of antibiotics.
- Salicylate influences the expression of these proteins and affects antibiotic susceptibility in a transient manner.