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      A genetic basis for Pseudomonas aeruginosa biofilm antibiotic resistance.

      Nature

      physiology, Animals, genetics, drug effects, Pseudomonas aeruginosa, Plankton, Phenotype, metabolism, Periplasm, Mutation, Microbial Sensitivity Tests, biosynthesis, Glucans, Drug Resistance, Bacterial, growth & development, Biofilms, Bacterial Proteins, pharmacology, Anti-Bacterial Agents

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          Abstract

          Biofilms are surface-attached microbial communities with characteristic architecture and phenotypic and biochemical properties distinct from their free-swimming, planktonic counterparts. One of the best-known of these biofilm-specific properties is the development of antibiotic resistance that can be up to 1,000-fold greater than planktonic cells. We report a genetic determinant of this high-level resistance in the Gram-negative opportunistic pathogen, Pseudomonas aeruginosa. We have identified a mutant of P. aeruginosa that, while still capable of forming biofilms with the characteristic P. aeruginosa architecture, does not develop high-level biofilm-specific resistance to three different classes of antibiotics. The locus identified in our screen, ndvB, is required for the synthesis of periplasmic glucans. Our discovery that these periplasmic glucans interact physically with tobramycin suggests that these glucose polymers may prevent antibiotics from reaching their sites of action by sequestering these antimicrobial agents in the periplasm. Our results indicate that biofilms themselves are not simply a diffusion barrier to these antibiotics, but rather that bacteria within these microbial communities employ distinct mechanisms to resist the action of antimicrobial agents.

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          Journal
          10.1038/nature02122
          14628055

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