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Antimicrobial Agents and Chemotherapy, September 1998, p. 2225-2231, Vol. 42, No. 9
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Influence of the TonB Energy-Coupling Protein on
Efflux-Mediated Multidrug Resistance in Pseudomonas
aeruginosa
Qixun
Zhao,1
Xian-Zhi
Li,1
Anita
Mistry,2
Ramakrishnan
Srikumar,1
Li
Zhang,1
Olga
Lomovskaya,2 and
Keith
Poole1,*
Department of Microbiology and Immunology,
Queen's University, Kingston, Ontario K7L 3N6,
Canada,1 and
Microcide
Pharmaceuticals, Inc., Mountain View, California
940432
Received 1 April 1998/Returned for modification 4 June
1998/Accepted 25 June 1998
TonB couples the energized state of the cytoplasmic membrane to the
operation of outer membrane receptors responsible for Fe(III)
siderophore uptake across the outer membrane of gram-negative bacteria.
A tonB mutant of Pseudomonas aeruginosa
deficient in iron siderophore uptake was shown in the present study to
be hypersusceptible to a wide variety of antibiotics, reminiscent of
the phenotype of mutants defective in the mexAB-oprM
antibiotic efflux operon. This was not related to influences of a
tonB mutation on the iron status of the cell, and indeed,
intrinsic antibiotic susceptibility and mexAB-oprM
expression were unaffected by iron levels in the growth medium. The
presence of tonB on a multicopy plasmid increased the level
of resistance of a MexAB-OprM+ strain but not that of a
MexAB-OprM
strain to a variety of antimicrobial agents.
mexAB-oprM expression was not, however, altered in a
tonB deletion mutant, indicating that any influence of TonB
on MexAB-OprM-mediated multidrug resistance was at the level of pump
activity. Consistent with this, drug accumulation assays revealed that
the tonB deletion mutant exhibited decreased levels of drug
efflux. Still, the multidrug resistance of a nalB strain
was not wholly abrogated by a tonB mutation, indicating
that it is likely not an essential component of the efflux apparatus.
Similarly, elimination of tonB from an nfxB strain only partially compromised MexCD-OprJ-mediated multidrug resistance. Intriguingly, the drug susceptibility of a
mexAB-oprM deletion strain was increased following deletion
of tonB, suggesting that TonB may also influence antibiotic
resistance mediated by determinants other than MexAB-OprM (and
MexCD-OprJ). Thus, TonB plays an important role in both intrinsic and
acquired antibiotic resistance in P. aeruginosa.
*
Corresponding author. Mailing address: Department of
Microbiology and Immunology, Queen's University, Kingston, Ontario K7L 3N6, Canada. Phone: (613) 545-6677. Fax: (613) 545-6796. E-mail: poolek{at}post.queensu.ca.
Antimicrobial Agents and Chemotherapy, September 1998, p. 2225-2231, Vol. 42, No. 9
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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