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J. Bacteriol., 11 1997, 7004-7010, Vol 179, No. 22
P Plesiat, JR Aires, C Godard and T Kohler
Testosterone (a strongly hydrophobic steroid) and testosterone
hemisuccinate (a negatively charged derivative) were used as probes to
investigate alterations in the outer membrane of Pseudomonas aeruginosa.
Diffusion rates of the steroids across the lipid bilayer were measured by
coupling the influx of these compounds to their subsequent oxidation by an
intracellular delta1-dehydrogenase enzyme. Wild-type cells of P. aeruginosa
(strain PAO1) were found to be 25 times more permeable to testosterone than
to testosterone hemisuccinate. The uptake of the latter compound appeared
to be partially dependent on the external pH, thus suggesting a
preferential diffusion of the uncharged protonated form across the cell
envelope. Using various PAO mutants, we showed that the permeation of
steroids was not affected by overexpression of active efflux systems but
was increased up to 5.5-fold when the outer membrane contained defective
lipopolysaccharides or lacked the major porin OprF. Such alterations in the
hydrophobic uptake pathway were not, however, associated with an enhanced
permeability of the mutants to the small hydrophilic molecule
N,N,N',N'-tetramethyl-p-phenylene diamine. Thirty-six agents were also
assayed for their ability to damage the cell surface of strain PAO1, using
testosterone as a probe. Polymyxins, rBPI23, chlorhexidine, and
dibromopropamidine demonstrated the strongest permeabilizing activities on
a molar basis in the presence of 1 mM MgCl2. These amphiphilic polycations
increased the transmembrane diffusion of testosterone up to 50-fold and
sensitized the PAO1 cells to hydrophobic antibiotics. All together, these
data indicated that the steroid uptake assay provides a direct and accurate
measurement of the hydrophobic uptake pathway in P. aeruginosa.
Copyright © 1997, American Society for Microbiology
Use of steroids to monitor alterations in the outer membrane of Pseudomonas aeruginosa
Laboratoire de Bacteriologie, Faculte de Medecine, Besancon, France. pplesiat@infrescom.fr
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