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Antimicrobial Agents and Chemotherapy, November 2007, p. 3908-3914, Vol. 51, No. 11
0066-4804/07/$08.00+0 doi:10.1128/AAC.00449-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

,1,2
Rimantas Daugelavi
ius,1,2 and
Dennis H. Bamford1*
Department of Biological and Environmental Sciences and Institute of Biotechnology, Biocenter 2, P.O. Box 56 (Viikinkaari 5), 00014 University of Helsinki, Finland,1
Department of Biochemistry and Biophysics, Vilnius University, M. K.
iurlionio 21, 03101 Vilnius, Lithuania2
Received 2 April 2007/ Returned for modification 30 April 2007/ Accepted 10 August 2007
Polymyxin B (PMB) is a cationic antibiotic that interacts with the envelopes of gram-negative bacterial cells. The therapeutic use of PMB was abandoned for a long time due to its undesirable side effects; however, the spread of resistance to currently used antibiotics has forced the reevaluation of PMB for clinical use. Previous studies have used enteric bacteria to examine the mode of PMB action, resulting in a somewhat limited understanding of this process. This study examined the effects of PMB on marine pseudoalteromonads and demonstrates that the frequently accepted view that "what is true for Escherichia coli is true for all bacteria" does not hold true. We show here that in contrast to the growth inhibition observed for enteric bacteria, PMB induces lysis of pseudoalteromonads, which is not prevented by high concentrations of divalent cations. Furthermore, we demonstrate that a high membrane voltage is required for the interaction of PMB with the cytoplasmic membranes of pseudoalteromonads, further elucidating the mechanisms by which PMB interacts with the cell envelopes of those gram-negative bacteria.
Published ahead of print on 20 August 2007.
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