Abstract
Trimethoprim-sulfamethoxazole (co-trimoxazole) is one of the antimicrobials of choice for the treatment of Stenotrophomonas maltophilia infections. The analysis of mutants either lacking or overexpressing the efflux pump SmeDEF shows that this efflux pump contributes to intrinsic and acquired co-trimoxazole resistance in S. maltophilia. Since SmeDEF can extrude a variety of antibiotics, selection with such antimicrobials, including quinolones, might also select for S. maltophilia co-trimoxazole resistance.
Copyright © 2015, American Society for Microbiology. All Rights Reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Anti-Bacterial Agents / pharmacology*
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Bacterial Proteins / genetics*
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Bacterial Proteins / metabolism*
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Drug Resistance, Bacterial / genetics*
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Membrane Transport Proteins / genetics*
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Membrane Transport Proteins / metabolism*
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Microbial Sensitivity Tests
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Mutation / genetics
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Quinolones / pharmacology
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Stenotrophomonas maltophilia / drug effects*
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Stenotrophomonas maltophilia / genetics
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Stenotrophomonas maltophilia / metabolism
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Trimethoprim, Sulfamethoxazole Drug Combination / pharmacology*
Substances
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Anti-Bacterial Agents
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Bacterial Proteins
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Membrane Transport Proteins
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Quinolones
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Trimethoprim, Sulfamethoxazole Drug Combination